Research Article

Natural Variation of the Amino-Terminal Glutamine-Rich Domain in Drosophila Argonaute2 Is Not Associated with Developmental Defects

  • Daniel Hain,

    Affiliation: Division of Cell and Developmental Biology, College of Life Sciences, University of Dundee, Dundee, United Kingdom

  • Brian R. Bettencourt,

    Affiliation: Alnylam Pharmaceuticals, Cambridge, Massachusetts, United States of America

  • Katsutomo Okamura,

    Affiliation: Sloan-Kettering Institute, Department of Developmental Biology, New York, New York, United States of America

  • Tibor Csorba,

    Affiliation: Wellcome Trust Centre for Gene Regulation and Expression, College of Life Sciences, University of Dundee, Dundee, United Kingdom

    Current address: Agricultural Biotechnology Centre, Godollo, Hungary

  • Wibke Meyer,

    Affiliation: Institut für Genetik, Heinrich Heine Universität, Düsseldorf, Germany

    Current address: Institute for Reference Materials and Measurements, Joint Research Centre European Commission, Geel, Belgium

  • Zhigang Jin,

    Affiliation: Sloan-Kettering Institute, Department of Developmental Biology, New York, New York, United States of America

  • Jason Biggerstaff,

    Affiliation: Boston University, Boston, Massachusetts, United States of America

  • Haruhiko Siomi,

    Affiliation: Department of Molecular Biology, Keio University School of Medicine, Tokyo, Japan

  • Gyorgy Hutvagner,

    Affiliation: Wellcome Trust Centre for Gene Regulation and Expression, College of Life Sciences, University of Dundee, Dundee, United Kingdom

  • Eric C. Lai,

    Affiliation: Sloan-Kettering Institute, Department of Developmental Biology, New York, New York, United States of America

  • Michael Welte equal contributor,

    equal contributor Contributed equally to this work with: Michael Welte, H.-Arno J. Müller

    Affiliation: Department of Biology, University of Rochester, Rochester, New York, United States of America

  • H.-Arno J. Müller equal contributor mail

    equal contributor Contributed equally to this work with: Michael Welte, H.-Arno J. Müller

    Affiliation: Division of Cell and Developmental Biology, College of Life Sciences, University of Dundee, Dundee, United Kingdom

  • Published: December 17, 2010
  • DOI: 10.1371/journal.pone.0015264


The Drosophila argonaute2 (ago2) gene plays a major role in siRNA mediated RNA silencing pathways. Unlike mammalian Argonaute proteins, the Drosophila protein has an unusual amino-terminal domain made up largely of multiple copies of glutamine-rich repeats (GRRs). We report here that the ago2 locus produces an alternative transcript that encodes a putative short isoform without this amino-terminal domain. Several ago2 mutations previously reported to be null alleles only abolish expression of the long, GRR-containing isoform. Analysis of drop out (dop) mutations had previously suggested that variations in GRR copy number result in defects in RNAi and embryonic development. However, we find that dop mutations genetically complement transcript-null alleles of ago2 and that ago2 alleles with variant GRR copy numbers support normal development. In addition, we show that the assembly of the central RNAi machinery, the RISC (RNA induced silencing complex), is unimpaired in embryos when GRR copy number is altered. In fact, we find that GRR copy number is highly variable in natural D. melanogaster populations as well as in laboratory strains. Finally, while many other insects share an extensive, glutamine-rich Ago2 amino-terminal domain, its primary sequence varies drastically between species. Our data indicate that GRR variation does not modulate an essential function of Ago2 and that the amino-terminal domain of Ago2 is subject to rapid evolution.


Argonaute proteins play key roles in diverse mechanisms of gene regulation from plants to fungi and animals, including humans. The Argonaute protein family is characterized by a stereotyped domain structure and has been divided into the Argonaute subfamily (related to Arabidopsis thaliana Argonaute) and the PIWI subfamily (related to D. melanogaster PIWI) [1], [2]. Organisms may contain a large number of different Argonaute encoding genes, currently with a maximum of 26 family members identified in C. elegans [3]. The presence of multiple, differentially expressed family members in a single species indicates diverse biological functions of Argonaute proteins.

A common feature of all Argonaute proteins is that they bind small RNAs and mediate silencing of target transcripts by translational inhibition or RNA degradation [4]. Argonaute subfamily proteins interact with siRNAs and/or miRNAs and in animals exert diverse functions during development of various somatic lineages. These functions range from selective degradation of unwanted maternal mRNAs in early development to the regulation of transcripts important for cell fate decisions during neuronal and muscle development as well as degradation of viral RNA in adult organisms [5]. An important function for the RNAi pathway was also demonstrated in innate immune response against viruses in animals and plants [6], [7], [8], [9].

Drosophila has proved to be an excellent model system for research on Argonaute protein function [10], [11], [12]. The Drosophila melanogaster genome encodes five Argonaute family members: Piwi subfamily members Aubergine (Aub), Piwi and Ago3 and the Argonaute subfamily members Ago1 and Ago2. Ago1 is essential for miRNA function, while Ago2 predominantly acts in the siRNA pathway [11], [13], [14]. Ago2 is the carrier of both exogenous and endogenous siRNAs, and functions in virus defense, restriction of transposable elements, and cleavage of mRNA targets [15]. Ago1 and Ago2 also have overlapping functions, e.g. in the control of segment polarity during embryogenesis [16].

Drosophila Ago2 is unique among the Argonaute subfamily: Its sequence is highly divergent and clearly distinct from other metazoan Argonautes (including Drosophila Ago1 and the four human Argonautes Ago1, Ago2, Ago3 and Ago4) or even Argonautes from fungi or plants [17]. It is a modular protein with the canonical PAZ and PIWI domains in the carboxy-terminal half and an amino-terminal half that is highly enriched in glutamine residues [16]. The carboxy-terminal region (820 amino acids) is broadly conserved in Argonaute family members from plants to fission yeast and vertebrates and has well-characterized biochemical functions, such as binding and cleavage of RNA [1]. In contrast, the amino-terminal portion (in the following referred to as the amino-terminal domain or NTD) is not well characterized. While the corresponding region is typically very short in most other family members (e.g. 24 aa in human Ago2), the Ago2 NTD in D. melanogaster is 397 amino acids long and encompasses long stretches of low sequence complexity (40% of all residues are glutamine). The majority of the NTD consists of two types of imperfect glutamine-rich repeats (GRR), called GRR1 (6 amino acid imperfect repeat) and GRR2 (23 amino acid imperfect repeat) ([16]; see below). Previous analysis of the drop out (dop) mutation suggested that altered GRR copy number disrupts Ago2 function and leads to maternal-effect lethality [16].

In the present paper, we demonstrate that ago2 is a complex locus that produces several distinct transcripts. The protein isoforms encoded by these transcripts have identical C-terminal regions that include the PAZ and Piwi domains. But while two long isoforms contain the unusual NTD, a previously uncharacterized short isoform lacks both types of amino-terminal GRRs, reminiscent of mammalian Argonaute proteins. We find that two ago2 mutant alleles widely employed as null alleles still express the short isoform. Using true null alleles, we show that the dop mutation is not allelic to ago2 and that GRR variation does not cause striking defects in embryonic development. In fact, we find extensive GRR repeat-number variation among D. melanogaster strains isolated from natural and laboratory populations as well as tremendous variability of the Ago2 NTD between insect species. These data suggest that this domain is subject to rapid evolution and has a non-essential, possibly modulatory function.

Results and Discussion

The ago2 locus generates transcripts encoding putative long and short isoforms

Gene annotation predicts that the ago2 locus gives rise to the two transcripts AGO2-RB and AGO2-RC (FlyBase, 6_2010). They are largely identical, but differ at their very 5′ ends, due to alternative splicing and the use of distinct transcription start sites (Fig. 1A). As a result, the two protein isoforms encoded by these transcripts, AGO2-PB and AGO2-PC, differ only by tiny unique stretches (6 or 9 amino acids) at their amino termini and have a 1208 amino acid region in common.


Figure 1. The ago251B and ago2414 alleles produce an alternative transcript encoding a putative short form of the protein.

(A) ago2 genomic organization indicating 8 exons of the two alternatively spliced gene products Ago2-RB and Ago2-RC (UTRs are indicated in orange; CDS is indicated in blue). Also shown is the extent of the chromosomal deletions generated by imprecise excision of the EP(3)3417 P-element insertion, located 12 bp downstream of the transcriptional start site (TSS) for Ago2-RB. The ago2414 allele creates a deletion of 2356 bp and ago2321 creates a deletion of 2514 bp. (B) Cartoon of genomic organization of Ago2-RB and the positions of the PCR primers (RB, TS, GM (forward and reverse, respectively), E5, and PZ). RT-PCR experiments using primer pairs as indicated; all PCR products were subjected to DNA sequencing. The RB/PZ primer pair amplifies a product of 3488 bp indicative of a transcript encoding for the long isoform; this product is only detected in w1118 and dop1, but not in ago251B and ago2414. GM/PZ amplifies a 2200 bp product, which is detected in all genotypes. The TS primer was designed to bind within the second intron. The TS/GM or TS/E5 primer pairs revealed products of the predicted sizes and sequences of an alternative transcript encoding for the short isoform (w1118 samples). All template polyA+ RNA was prepared from ovaries. (C) 10 µg total RNA from adult flies was subjected to Northern blotting. The ago2414 allele produces detectable ago2 transcripts whereas no transcript was detected in ago2321 homozygous flies. Note that the probe was designed against the downstream of ago2454 deletion and a putative truncated mRNA was detected in ago2454 homozygous flies. (D) Quantitative RT PCR comparing expression of transcripts encoding Ago2long and Ago2short from total RNA of 3–5 hrs embryos. Primer pairs were designed to specifically amplify PCR products of transcripts encoding for the short and long isoform, respectively. (E) UAS::GM07030-HA was expressed in embryos using maternal α4-tubulin64C::Gal4 (mat67;mat15) and proteins were immunoblotted using anti-HA antibody. w1118 embryos were used as a control. The arrowhead indicates one specific protein band at around 85 kDa indicative of HA-tagged Ago2short (LC - loading control).


To functionally characterize Ago2, many studies employ the two putative null alleles ago251B and ago2414. These alleles represent two independently derived deletions that eliminate the first two annotated AGO2-RB exons and part of the third intron (Fig. 1A; [11], [18]). As they delete the annotated translational start sites for both AGO2-RB and AGO2-RC, these alleles are expected to abolish all ago2 expression [11], [18].

To test this prediction directly, we performed RT-PCR analysis with various primers across the ago2 locus (Fig. 1B). Experiments that involved a primer specific for exon 1 (primer RB) failed to detect any ago2 transcripts in these alleles (Fig. 1B), confirming the absence of AGO2-RB and AGO2-RC. However, when we employed primers from exons 3 through 7, we detected amplification products in these supposed null alleles. These products are not due to contamination with genomic DNA templates as their size was the same as in the wild type and sequencing confirmed that they represent correctly spliced transcripts. Furthermore, Northern analysis of total RNA of adult flies confirmed the presence of ago2 transcript in ago414 (Fig. 1C). These results indicate the presence of previously unannotated transcripts in ago251B and ago2414.

These transcripts could also be detected with primers upstream of the third exon splice site, a region annotated as intronic for AGO2-RB and AGO2-RC (Fig. 1B, primer TS). Apparently, the alternate transcripts originate 5′ to exon 3. This property makes it possible to design isoform-specific primers to examine the expression of the alternative transcript and of AGO2-RB/AGO2-RC separately. Using these primers, we found that wild-type flies express both types of transcripts. Quantitative RT-PCR analysis on samples from adult flies indicates that the shorter transcript is expressed approximately 30% less than AGO2-RB/AGO2-RC (Fig. 1D).

These alternative transcripts are predicted to encode a shorter protein isoform of Ago2, in the following referred to as Ago2short. Since we have not been able to verify protein production from this transcript in vivo, we tested whether a cDNA encoding Ago2short can in principle produce a protein of the expected size. The Berkeley Drosophila genome project (BDGP) had isolated an EST clone, GM07030, which is predicted to encode Ago2short. We generated a transgene, in which HA-tagged GM07030 is driven under the control of UAS elements. Uniform expression of this transgene in the embryo results in a protein product of approximately 85 kDa, consistent with the predicted molecular weight of Ago2short (Fig. 1E).

A truncated Ago2 protein lacking GRRs was recently shown to support full biochemical reconstitution of RISC indicating that the N-terminal region does not contain domains that are essential for core RNAi [19]. In the lack of an NTD, Ago2short is reminiscent of the mammalian Argonautes; indeed, BLAST comparisons reveal significant similarity between Ago2short and human Ago2 throughout essentially the entire length of the proteins (not shown). We conclude that the ago2 locus has the potential to encode at least three protein isoforms, only two of which encompass the unusual NTD that sets D. melanogaster Ago2 apart from other family members.

Identification of true null alleles of ago2

The available putative null alleles of ago2 remove 5′ exons with limited coding potential [11], [18]. The existence of an alternative isoform implies that ago251B and ago2414 may retain some Ago2 function. Indeed, although Northern analysis of embryos had suggested that ago2414 is transcript null [11], we observed substantial amounts of nearly full length transcript in adult flies (Fig. 1C).

We therefore examined additional excision events derived from EP(3)3417 to identify bona fide Ago2 null alleles. This screen identified two alleles that were transcript null in the adult, ago2321 and ago2454 (Fig. 1C). These alleles contain the same 5′ breakpoint located 34 bp downstream of the transcriptional start site of AGO2-RB, but have different 3′ breakpoints (Fig. 1A). The deletion in ago2321 removes 2514 bp and is very similar to ago2414, but retains a section of the original EP element; this insertion may contribute to why it is transcript null. ago2454 carries a deletion of 5750 bp and accumulates a truncated transcript consistent with this deletion. This deletion removes the PAZ domain and much of the PIWI domain, and is therefore unquestionably a null allele.

Homozygotes of ago2321 and ago2454 stocks were viable, but unlike ago251B and ago2414, they exhibited low fertility in both males and females. 55% of embryos obtained from ago2321 homozygous mothers did not hatch (n = 221), while ago2454 homozygous females did not lay any eggs. 50% ovaries from ago2321 and 90% ovaries from ago2454 homozygotes are rudimentary. Surprisingly, none of the phenotypes seen in ago2321 or ago2454 homozygotes except male sterility were seen in ago2321/ago2454 trans-heterozygotes. Moreover, ago2321/Df or ago2454/Df hemizygotes (using the molecularly defined deficiencies Df(3L)ED218 and Df(3L)BSC5580) displayed none of the above-mentioned phenotypes. Therefore, the fertility phenotypes observed in ago2321 and ago2454 homozygotes are likely attributable to background mutations. While a detailed analysis of these novel ago2 null alleles is beyond the scope of this paper, an exciting prospect for the future is to determine whether these alleles corroborate or extend other phenotypes that were previously reported for ago2414 or ago251B alleles. Such phenotypes include defective heterochromatin formation [20], defective neuromuscular junction and egg chamber development [21], and defects in embryonic syncytial divisions and pole cell formation [22]. The partial penetrance of these defects in ago2414 and ago251B homozygotes might result from residual Ago2 function due to Ago2short expression.

Ago2 is the carrier of endogenous small interfering RNAs (endo-siRNAs) [15]. Although a cohort of endo-siRNA substrates have been identified, along with a number of targeted transcripts, the biological function of endogenous RNAi remains poorly defined. The major phenotypes are molecular in nature, and include upregulation of transcripts derived from transposable elements and certain direct targets of hairpin RNA-derived siRNAs [23], [24], [25], [26], [27], [28]. A detailed analysis of the true ago2 null alleles ago2454 and ago2321 might therefore provide the most stringent test of the overall requirements of the endo-siRNA pathway for various aspects of development.

GRR variation does not noticeably disrupt development

Our expression analysis indicates that D. melanogaster is able to produce Ago2 variants with and without the glutamine-rich NTD. This observation suggests that the NTD serves some important function as its expression is retained even though NTD-less forms can apparently be produced.

Our previous work had suggested a biological role for the NTD. We discovered variants in the GRR pattern and found that they were associated with severe disruption of embryonic development [16]. In particular, we had found that embryos from mothers homozygous for dop mutations show delays in cellularization, display abnormal transport of lipid droplets, and fail to hatch. Sequencing of genomic DNA of the dop1 allele revealed that in this strain ago2 has 4 copies of GRR1 and 10 copies of GRR2; in contrast, the precursor chromosome (red e) exhibited the expected 4xGRR1/11xGRR2 pattern of the published wild-type sequence. For an independently derived dop allele (dop46), ago2 displayed 3xGRR1 and 11xGRR2. A functional connection between dop and ago2 was suggested by the observation that a chromosomal deletion (Df(3L)XG9) uncovering ago2 does not complement dop alleles and that the maternal lethality of dop mutations is partially rescued by expression of an ago2 cDNA [16]. Finally, dop alleles genetically interact with other genes involved in RNA silencing. These results suggested that deviation from the wild-type number of GRRs severely impairs Ago2 functions and results in developmental defects [16].

The identification of true null alleles of ago2 (above) enabled us to perform a stringent genetic test of this idea. dop homozygous as well as dop/Df(3L)XG9 mothers are completely sterile. However, mothers carrying one dop allele (either dop1 or dop46) and one ago2 null allele (ago2321 or ago2454) were fertile. For example, the embryos obtained from dop1/ago2321 heterozygotes hatched at rates similar to wild type (Fig. 2A).


Figure 2. Null alleles of ago2 complement dop1 mutants.

(A) Percentage of larvae hatching from indicated genotypes (n>300 per genotype). (B) Bright-field images of post-gastrula embryos (stage 10) show that the periphery of dop1 mutant embryos is abnormally transparent compared to wild type (wt) [16]. These transparency changes are characteristic of altered lipid-droplet distribution [57]. Embryos obtained from mothers transheterozygous for dop1 and either ago2321 or ago2454 exhibit a normal pattern lipid-droplet distribution. (C) Immunolabeling of the membrane protein Neurotactin (red) and DNA (DAPI, blue) in embryos during and after cellularization. Embryos from dop1 homozygous females exhibit a severe delay in membrane ingression marked by the absence of Neurotactin staining at the interface between adjacent nuclei [16]. Embryos from dop1/ago2321 transheterozygous mothers show normal membrane ingression during cellularization.


The embryos from transheterozygous (ago2null/dop) mothers also did not exhibit the developmental defects characteristic of dop mutant embryos. Embryos obtained from dop1 or dop46 homozygous mothers show normal syncytial development, but plasma membrane growth during cellularization is strongly delayed (Fig. 2B; [16]). Embryos obtained from transheterozygous mothers do not display such delay in cellularization (Fig. 2B). Furthermore, lipid droplets are severely mislocalized in dop mutant embryos during germ-band extension (Fig. 2C). In contrast, lipid-droplet distribution in embryos from ago2null/dop mothers is similar to the wild type (Fig. 2C). These results demonstrate that dop is not allelic to ago2. In addition, there is no evidence that ago2 with non-standard GRR pattern results in developmental defects.

GRR variation does not affect RISC assembly

Depletion of Ago2 from cell lines or flies results in a complete block of the RNAi response [10]. Furthermore, biochemical data indicate that Ago2 is an essential and sufficient component of RISC, the central machinery that directs mRNA cleavage by siRNAs [10], [12], [29], [30]. Ago2long is essential for this process, because ago251B or ago2414 homozygotes lack most, if not all, of the RNAi response [11], [16]. Since the dop1 chromosome (characterized by the 4/10 GRR ago2 pattern) exhibits a mild suppression of experimental RNAi in vivo [16], variation in Ago2long might modulate the formation of RISC.

To test this possibility directly, we assayed RISC-formation in vitro in embryo extracts obtained from wild-type and dop1 embryos, using gel shift experiments with siRNA [31]. RISC formation as observed by assembly of complexes over time was unimpaired in dop1 mutant embryos when compared to wild type (Fig. 3). We therefore conclude that the variation of GRR pattern in dop mutants does not affect formation of RISC. This finding is consistent with reports that recombinant Ago2 lacking the first 277 aa of the NTD (this truncation removes all GRR1 and seven GRR2 repeats) supports RISC assembly [19].


Figure 3. Comparison of RISC formation in wild type and dop1 mutant embryos.

In-vitro silencing complexes formation was analyzed by incubating dilutions of cell free extracts (conc: µg/µl total protein) of wild type or dop1 Drosophila embryo extracts with pre-labelled siRNA. The formed silencing complexes were separated on a native acrylamide gel. The free-siRNAs and the R1, R2 and holo-RISC complexes are shown (The star marks an unknown band).


GRR copy number varies extensively between different fly strains

The complementation tests above demonstrate that dop and ago2 represent distinct genes. Yet, in two independently derived lines, dop mutations are associated with changes in the GRR pattern of ago2 [16]. This fortuitous association might be explained if changes in the GRR pattern of ago2 occur at high frequency.

We therefore examined GRR1 and GGR2 copy number in twenty-two laboratory strains of diverse origins. In these strains, GRR1 copy number varied between 2 and 4, and GRR2 copy number between 10 and 16 (Table 1, Fig. 4, Fig. S1, and data not shown). For example, copies of the wild-type strain Oregon R obtained from two different laboratories had 4x GRR1 and 13x GRR2 or 3x GRR1 and 16x GRR2, respectively. Various combinations of GRR1 and GRR2 copy numbers can occur. In the following, we refer to these combinations as GRR haplotypes.


Figure 4. Different Ago2 GRR haplotypes in Drosophila melanogaster.

(A) The domain structure of Ago2_PB protein isoform, according to FlyBase version FB2009_2. The amino-terminal half contains glutamine-rich repeats (GRR), shown in more detail in (C). The carboxy-terminal half contains the PAZ and the PIWI domains (bar indicates 100 amino acids). (B) The copy number of GRR2 repeats varies between various laboratory strains. Using flanking primers, the genomic region encompassing the GRR2 repeats was amplified by PCR in various laboratory strains, or in the progeny of crosses between those strains. CS = Canton S; TM6B = balancer chromosome (tested over a deficiency encompassing the ago2 locus); OR* and OR** are Oregon R strains obtained from two independent sources. Below the gel image is the number of GGR2 repeats as determined by sequencing. (C) Different ago2 haplotypes determined by genomic DNA sequencing (see Table 1 for a complete list of all haplotypes determined in this study).


Table 1. GRR pattern in Ago2 in different D. melanogaster strains.


To assess if variation in GRR copy number is a consequence of extended laboratory culture, we examined ten strains recently isolated from the wild. These strains are isogenic for third chromosomes that had been extracted from a single wild North American population [32]; we analyzed their GRR haplotypes within five years after they had been established. These strains exhibited GRR haplotype diversity equal to or greater than that found in the long-established laboratory strains (Table 1).

Our results indicate that in D. melanogaster the NTD of Ago2 can undergo drastic changes in length and sequence composition. As we have not attempted a comprehensive survey, we suspect that GRR variation is not restricted to the haplotypes we identified. Considering just the instances listed in Table 1, NTD length can vary by over 35% (from 368 to 506 amino acids). These changes in the NTD likely arise by repeat expansion and contraction mediated by unequal crossing over [33]. Interestingly, the glutamine fraction of the NTD remains fairly constant (~40%).

Failure to detect phenotypic consequences of NTD variability

The NTD variability we uncovered provides an independent test whether GRR copy number and the dop phenotype are linked. Many of the strains in Table 1 are homozygous viable and at least grossly normal, suggesting that the exact composition of the amino-terminal domain of Ago2 is nonessential for viability and that many GRR haplotypes are compatible with normal development. In particular, the Tai255.1 strain, a wild-type D. melanogaster strain isolated 1983 at Ivory Coast [34] had the same 3/11 GRR haplotype found in the dop46 allele. However, unlike dop1 or dop46 embryos, Tai255.1 embryos develop apparently normally (Fig. 5). They cellularized normally and displayed normal lipid-droplet transport (Fig. 5A,B). We therefore conclude that GRR variation in ago2 does not disrupt embryogenesis and in particular is not responsible for the developmental defects observed in dop mutants.


Figure 5. Altered GRR pattern is not associated with developmental defects characteristic of dop alleles.

(A) Kymographs from time-lapse microscopy of w1118, Tai255.1 and dop1 embryos. Upper panels show primary data and lower panels indicate the embryo surface membrane (red) and the ingressing plasma membrane (yellow) over time (t). In the wild type (wt), membrane ingression is initially slow at 0.29 µm/min) and then increased in the second phase to 0.72 µm/min. Similar values were observed for Tai255.1. dop1 mutant embryos exhibit a strong reduction in membrane ingression during slow phase (0.12 µm/min); fast phase is normal. (B) Bright-field images of post-gastrula stage embryos indicating distribution of lipid droplets in wild-type (wt), Tai255.1 and dop1 mutant embryos. In wild-type and Tai255.1 embryos, the periphery of the embryo is opaque due to the presence of lipid droplets within the ectoderm and mesoderm cell layer. dop1 mutant embryos exhibit a characteristic lipid-droplet transport defect indicated by a concentration of lipid droplets in the center of the embryo and a transparent embryonic periphery.


We next examined if GRR variation influences expression of long and short Ago2 isoforms. Eight wild type third-chromosome extracted 3CPA strains all express both long and short ago2 transcripts (Fig. 6). We conducted quantitative real-time PCR using ago2 long- and short-specific primers and cDNA prepared from 3-day old females [35]. ago2long expression varied significantly among the strains (ANOVA; p<0.05), and was consistently higher than ago2short expression (Fig. 6; average ago2long expression is 11% higher than ago2short). In contrast, ago2short expression did not vary significantly among the strains, and we detected no correlation between ago2long and ago2short expression levels. Last, there was no obvious relationship between GRR haplotypes and ago2long or ago2short expression in these strains. These results suggest independent regulation of transcripts for ago2long and ago2short.


Figure 6. Expression of ago2short and ago2long in wild-type D. melanogaster strains.

Levels of Ago2long (blue) and Ago2short (red) in the 3CPA strains. Each symbol represents mean expression level relative to RpL32, indicated as ratio of qtPCR critical thresholds (“CT”). Bars represent one SEM. X axis denotes strain.


In summary, we find no evidence that GRR variation is associated with dramatic changes in embryonic development or survival, in RISC formation or with changes in isoform expression. It is conceivable that GRR variation does not have any functional consequences and simply arises as “noise” due to the propensity of repeat regions to undergo unequal crossing over. Alternatively, GRR variation may be involved in more subtle functions of Ago2 than the ones tested here. While RISC formation per se can occur in the absence of most of the GRRs [19], regulation of Ago2 activity or efficient recognition of certain targets might be modulated by the NTD. For example, the long Ago2 isoform, which includes the NTD, is implicated in anti-viral responses as the ago2414 allele, which still expresses the short Ago2 isoform (above), exhibits strongly impaired host defense against viruses [7]. Future population-genetic and functional tests of Ago2 should therefore examine a range of complete ago2 haplotypes or, at a minimum, carefully define which “wild-type” version of Ago2 is being analyzed.

Extensive remodeling of the NTD between closely related species

Previous studies have uncovered unusually high variability in non-NTD regions of Ago2 [36], [37]. Comparison of the C-terminal 839 amino acids of Ago2 (i.e. largely excluding the NTD) in pairs of recently diverged Drosophila species revealed rapid evolutionary changes. These observations placed ago2 among the fastest evolving genes in Drosophilids, along with other components of the RNAi pathway [36]. It was proposed that this reflects adaptive evolution in response to changes in viral pathogens, as part of a virus-host arms race [37]. The observed changes in these RNAi pathway genes indeed bear the signature of positive selection [36].

The previously described evolutionary changes in Ago2 are concentrated in regions of unknown function [36]. In contrast, regions of Ago2 associated with core functions are conserved across all Drosophila species. The function of the NTD is also unknown. We therefore examined the NTDs in closely related species to determine whether their sequence evolution matches the former or latter pattern.

For this analysis, we focused on the three species most closely related to Drosophila melanogaster, namely Drosophila simulans, Drosophila mauritiana, and Drosophila sechellia. These species diverged <1 Mya (sechellia versus simulans) or ~2.3 Mya (D. melanogaster versus D. sechellia/simulans/mauritiana lineages) ago from each other, and the sequences of most genes are highly conserved in all four species [38], [39].

We first examined the DNA sequences that correspond to exon 3 of ago2 in D. melanogaster. Here, this exon encodes 330 amino acids of the NTD (including all GRR2 repeats) plus the following 92 amino acids, whose sequence is conserved in Argonautes from fungi, plants and animals. The latter, non-NTD stretch displayed very high amino acid sequence conservation between the four Drosophila species (Fig. S2, S3, and data not shown). And in each of the four species, the sequence immediately 5′ to this conserved region has the potential to encode glutamine-rich, repetitive stretches, but the exact sequence is highly divergent ([16], and Fig. S2). For example, the 23 aa GRR2 repeats characteristic of D. melanogaster are not apparent in any of the other three species. This observation suggests that NTDs can change drastically between even closely related species.

As the Ago2-encoding genomic sequences of D. simulans and D. mauritiana were nearly identical but differed from both D. sechellia and D. melanogaster, we performed a detailed comparison of the entire NTD between D. melanogaster, D. simulans and D. sechellia. The analysis above does not reveal the full extent of the NTDs or if these putative NTDs are indeed expressed. We therefore predicted possible upstream exons and designed primers in these exons and in exon 5 for RT-PCR analysis. For both D. simulans and D. sechellia, this strategy allowed us to amplify cDNA fragments spanning these exons; sequencing revealed that these fragments indeed encompass the putative exon 3, including the highly variable glutamine-rich stretches. Thus, like D. melanogaster, these species express unusual Ago2 NTDs.

The NTDs of the three species differ extensively from each other in length (D. sechellia: 211 aa; D. simulans: 277 aa; D. melanogaster 368 to 506 aa (Table 1)); their glutamine content, however, was fairly similar (36–40%) (Table 2; Fig. S3). These length differences do not arise from variation in copy numbers of similar repeats, as between distinct D. melanogaster strains (Table 1). Rather, NTD organization is quite different between species. The primary sequences of the simulans and sechellia NTDs are clearly related; both species contain a highly similar sequence of ~118 aa. But D. simulans Ago2 has imperfect, tandem copies of this sequence while D. sechellia Ago2 has a single copy (Fig. S2B). Instead, in D. sechellia Ago2, a 15 aa stretch internal to the 118 aa region is repeated three times. Neither the 118 aa nor the 15 aa repeat displays striking similarity to the 6 aa (GRR1) or 23 aa (GRR2) repeats in D. melanogaster. In contrast, the remainder of the Ago2 sequence in all three species is highly similar and can easily be aligned (Fig. S3). Thus, the primary sequence of the NTD is extremely variable, much more so than the rest of the protein (which already is among the most rapidly evolving proteins in Drosophila [36]).


Table 2. NTD of Ago2 orthologs in Drosophila species.


In D. melanogaster, the NTD displays drastic intra-specific variation (Table 1). To test if similar variability might occur in D. simulans, we amplified by PCR the genomic region corresponding to exon 3 from nine different strains and sequenced the PCR fragments. In total, we recovered five haplotypes that vary from each other by small deletions and insertions (Fig. S2A). We conclude that the NTD evolves rapidly both within and between species.

The NTD of Ago2 is highly variable throughout insects

In the genus Drosophila, nearly full genome sequences are available for nine additional species [40]. This resource provides an opportunity to examine the pattern of Ago2 evolution across longer evolutionary times, on the order of 50 Mya. We first identified all Argonaute family members in the predicted proteomes of all twelve species, by reciprocal blastp best-hit analysis and comparison of FlyBase annotations in all 12 species. We conducted multiple alignment of the protein sequences, neighbor-joining tree building and 1000 bootstrap trials via CLUSTALX (data not shown). Examination of the phylogram revealed a subset of these proteins as most closely related to Ago2 of D. melanogaster, clearly separate from Ago1, Piwi, Aubergine, and Ago3 orthologs. Interestingly, D. willistoni had two Ago2 paralogs and D. pseudoobscura and D. persimilis each had five Ago2 paralogs (see also Fig. 7). Multiple Ago2s in a single genome have also been reported for the mosquito Culex quinquefasciatus [41] and the flour beetle Tribolium castaneum [42] (Table 3). Presumably, multiple ago2 genes in a single organism allow those variants to be adapted for specific tasks. We speculate that in D. melanogaster the multiple isoforms generated from a single ago2 gene allow similar specialization.


Figure 7. Rooted neighbor-joining phylogram of Ago2 proteins.

Tree is rooted with Homo sapiens Ago2. Branch lengths (genetic distance) indicated by ruler. Numbers at nodes indicate supportive number of 1000 bootstrap trials. Nodes labeled with D indicate gene duplications. The genus Drosophila is indicated by a black bar. Species designations: Hsap, Homo sapiens; Dpul, Daphnia pulex; Bmor, Bombyx mori; Apis, Acyrthosiphon pisum; Phum, Pediculus humanus; Amel, Apis mellifera; Nvit, Nasonia vitripennis; Tcas, Tribolium castaneum; Cqu, Culex quinquefasciatus; Aae, Aedes aegypti; Dgri, Drosophila grimshawi; Dmoj, D. mojavensis; Dvir, D. virilis; Dwil, D. willistoni; Dana, D. ananassae; Dmel, D. melanogaster; Dsim, D. simulans; Dsec, D. sechellia; Dere, D. erecta; Dyak, D. yakuba; Dpse, D. pseudoobscura; Dper, D. persimilis.


Table 3. NTD of Ago2 orthologs in other species.


The protein annotation for the 11 non-melanogaster genomes employs a consensus between eight distinct gene prediction algorithms [40]. For most of the Ago2 candidates, either this consensus or at least one of the individual algorithms indicated the presence of a glutamine-rich NTD, suggesting that such amino-terminal domains are common throughout the genus. In total, 18 out of the 21 Ago2 sequences in Table 2 have an NTD of more than 240 amino acids and an NTD glutamine content above 12%. Although the presence of these NTDs will have to be independently confirmed in the future, for several of these candidates, cDNA or microarray evidence support that the NTD region is indeed expressed (Table S1).

Although many of these predicted Ago2 proteins have glutamine-rich NTDs, the primary sequence, length and glutamine content vary greatly between family members (Table 2, Fig. S4). This is even true for Ago2 paralogs in the same species, such as for the Ago2s of D. willistoni that have NTDs of 244 and 356 amino acids, respectively. And some of the D. persimilis and D. pseudoobscura copies even seem to lack a glutamine-rich NTD entirely. In addition, there are radical changes in repeat organization between species [16]. For example, in various Ago2s, we identified repeats of 11, 12, 13, 16, 22 and 31 amino acids in length. Even in the sister species D. persimilis and D. pseudoobscura which diverged ~0.5 Mya ago [43], the closely related Ago2 pair Dpse\Ago2c and Dper\Ago2c are identical across much of the NTD and the rest of the coding sequence, but are distinguished from each other by unique repeats (Fig. S5).

To determine if Ago2 NTDs are found outside the genus Drosophila, we searched various databases for Ago2 candidates and identified them in a wide variety of insect species, including flies, beetles, bees, wasps and lice, and even the crustacean Daphnia pulex (Fig. S4). A comparison with Argonaute family members from fungi, plants and animals (i.e., the dataset analyzed in [17]) indicated that insect plus Daphnia Ago2s are a monophyletic assemblage, well supported by bootstrap trials (data not shown). As previously noticed for D. melanogaster Ago2 [17], this entire clade is highly divergent and distinct from all other Argonautes. And like the Drosophila Ago2s, most members of this clade are predicted to carry glutamine-rich amino-terminal domains ([16], Fig. 7, Fig. S4, Table 3). In several instances, cDNA data support that these NTDs are expressed (Table S1). These domains are often, but not always, organized as multiple copies of imperfect repeats. As in the genus Drosophila, the lengths and sequences of these repeats vary substantially ([16], Fig. S4), and the NTDs overall do not display extensive similarity in primary sequence. Thus, highly variable Ago2 NTDs are apparently ancient and predate the origin of insects.

At the moment, it is impossible to determine whether drift or selection is the primary determinant of this variability. It is conceivable that the dramatic changes in NTD primary sequence are simply a consequence of the high instability of repetitive DNA sequences. If the NTD has no function, it may be free to vary with little constraints. In this scenario, selective sweeps due to positive selection on the rest of the Ago2 sequence, e.g. as frequency-dependent adaptation of the anti-viral response [36], may cause certain NTD haplotypes that happened to be present in those ago2 variants to rise in frequency via hitchhiking. Indeed, the number and heterozygosity of NTD alleles in the natural PA population is striking, especially when compared with other protein-coding repeats which may experience similar selective pressures. Considering the unique GRR1/GRR2 haplotypes listed in Table 1 (excluding missing data), there are 7 NTD alleles segregating among the PA strains. Heterozygosity, measured as one minus the sum of the allele frequencies, is 0.815. A recent survey of 58 protein-coding repeats in the same strains found lower diversity overall [44] the mean and maximum number of alleles were 2.83±0.2 and 8, respectively. Mean and maximum heterozygosity in the same survey were 0.457±0.03 and 0.83. This survey considered primarily homotypic amino-acid repeat loci, not mixed or “minisatellite” repeats as are found in the Ago2 NTD. Analyses of mixed protein-coding repeats in natural D. melanogaster populations are less common. The best-studied example involves the period (per) gene, which harbors a Thr-Gly repeat of varying length that is subject to strong natural selection imposed by photoperiod and climate [45]. A large survey of Australian populations found 8 Per Thr-Gly alleles segregating, with overall heterozygosity of 0.640 [46]. Thus, Ago2 NTD intraspecies variability is among the highest measured for protein-coding repeats in D. melanogaster, with very high heterozygosity consistent with selection-mediated maintenance of allele frequencies. Unlike per, however, no clear phenotypic basis for selection on NTD alleles is evident. To determine whether and how selection operates on the NTD vs. linked Ago2 regions, future studies should survey natural variability and linkage disequilibrium throughout the entire ago2 locus. Such studies will greatly benefit from recent efforts to sequence multiple D. melanogaster genomes.

Glutamine-rich NTDs of low sequence complexity are present across many insect species, even in species that are apparently able to generate Ago2 variants lacking the NTD (such as Ago2short in D. melanogaster and Ago2e in D. persimilis and pseudoobscura). We therefore favor the hypothesis that the NTD provides an important regulatory activity. Given the role of Ago2 in the defense against viruses [7], [9], it is an intriguing possibility that NTD variability modulates anti-viral responses. It will be revealing to test if the survival after viral challenge is different in D. melanogaster strains expressing endogenous Ago2 or Ago2 variants in which the NTD is deleted or replaced by the NTD of other insect species.

How the NTD might modulate the biological function of Ago2 is an exciting question for the future. A possible paradigm comes from the analysis of Trypanosoma brucei Ago1: Here, the amino-terminal 68 amino acids contain ten arginine-glycine rich motifs [47]. This so-called RGG domain is involved in the association of TbAgo1 with poly-ribosomes, an association required for an efficient RNAi response in this organism [48]. Intriguingly, the TbAgo1 RGG domain and the NTDs of arthropod Ago2s are all characterized by low sequence complexity and are likely to be intrinsically unstructured (based on RONN algorithm predictions ([49], data not shown). As intrinsically unstructured domains have been proposed as protein interaction domains [50] and changes in the number of glutamine-rich repeats can modulate interaction strength [51], [52], RGG or NTD variation might modulate the affinity of the Argonaute protein to particular targets. Indeed, mutant versions of TbAgo1 show progressively stronger RNAi responses, the more copies of the RGG motif are present [48].


The evolution of the Argonaute protein family resulted in members with specific tasks in small RNA functions within a single organism. Here we uncover additional complexity: Many insects express multiple Ago2 variants, either from independent genes or by generating multiple isoforms from a single gene. In addition, there is variation between different individuals of the same species, due to extensive variation in NTD organization. The functional significance of this variation remains unknown; we find that it does not grossly alter embryonic development or RISC assembly. But given the known role of Ago2 in protection against viruses, we speculate that this variability might allow fine-tuning of anti-viral responses. Such a modulatory role of the NTD would also be consistent with the rapid evolution of this domain, as observed in comparisons across insects. A potential association between NTD haplotype and Ago2 activity might provide novel insights into the plasticity of RNAi pathways in general and the innate viral response mechanisms in particular.

Materials and Methods

Drosophila strains and culture

Drosophila strains and embryos were cultured under standard laboratory condidtions. The following strains were used in this study: Oregon R, Canton-S (gift from L. Griffith), ago251B (gift of F.-B. Gao), ago2414, ago2454, ago2321. Screening of deletion mutants was carried out as previously described [11]. The EP transposon in the EP(3)3417 line was mobilized by crossing EP(3)3417 virgins with males possessing Δ2-3 transposase. Deletions were determined as described previously [11]. The D. melanogaster 3CPA strains were donated by B.P. Lazzaro and had been established in 2001 via extracting 3rd chromosomes segregating in a single Pennsylvania (USA) population over balancers and crossing into a common background [32]. D. melanogaster strains Tai255.1, w-14 melbourne and Oregon R** as well as D. simulans strains Oxnard, Tsimbazaza, vermilion, maz1, maz6 and C167.4 were a gift from H. Hollocher. These strains are described in Sainz et al. [53]. Additional strains were obtained from the Tucson Drosophila Stock Center: three D. simulans strains (sim1 = #14021-0251.48, sim2 = #14021-0251.047, sim3 = #14021-0251.004), one D. mauritiana strain (#14021-0241.46) and two D. sechellia strains (#14021-0248.08, #14021-0248.25). All other strains in Table 1 were obtained from the Bloomington Drosophila Stock Center.

Quantitative real-time PCR

Groups of 15 female flies aged 3-5 days were anesthetized under light CO2 and flash-frozen in liquid N2. Total RNA was prepared from each group, and cDNA was synthesized using oligo-dT primers according to standard protocols (see Bettencourt et al. 2008). Three replicate preparations were obtained for each of the 3CPA strains in Figure 6. QrtPCR was conducted using primers specific for ago2long and ago2short; sequences are available upon request. The ribosomal protein gene RpL32 was also examined as a control according to Bettencourt et al. (2008). A minimum of two replicate PCR reactions per strain/gene were conducted. Reactions were conducted and analyzed on a BIO-RAD myIQ thermocycler using a standard 40-cycle protocol, and amplification products were verified via electrophoresis and melt-curve.

In vivo observations and immunohistology

For in vivo observation, embryos were collected and staged on yeasted apple juice plates and mounted in halocarbon oil 27 (Sigma-Aldrich) on microscope slides. Video-microscopy was performed on a Zeiss (Germany) microscope equipped with Nomarski optics, and time-lapse movies were taken using the OpenLab software (Improvision, UK). For immunohistology, embryos were either heat-fixed or fixed using modified Stefanini's fixative and stained with antibodies essentially as described elsewhere [54]. The following antibodies were used: mouse anti Neurotactin (DSHB; Iowa, USA); mouse anti Arm [55]. All secondary fluorochrome conjugated antibodies were from Dianova (Germany) or Molecular Probes (Eugene, OR). Imaging was performed on a Leica SP2 Confocal microscope, and image processing was performed with Adobe Photoshop.

Molecular Biology

Molecular cloning was performed following standard protocols. RT-PCR was performed using ‘one Step RT PCR kit’ (Qiagen, Germany) with embryonic poly A+ RNA as templates. Primer sequences are available upon request. Products from RT-PCR were confirmed by sequencing (Seqlab, Göttingen, Germany). GenBank accession numbers of full-length cDNA for D. melanogaster ago2 are BT003546 (EST RE04347, RB isoform) and BT099682 (EST RE36670, RC isoform). In addition, the sequence of the EST GM07030 (GenBank accession number AY094751) is consistent with expression of the ago2short isoform. PCR to analyze NTDs in D. melanogaster, simulans, mauritiana and sechellia was performed with primers located in introns surrounding exons 2 and 3 of ago2, respectively. Protein extraction and immunoblotting was performed as described before [16].

Northern blotting

RNA samples were prepared from 2-4-day old male flies using Trizol. 10 µg total RNA was loaded in each lane on a denaturing agarose gel and transferred to Genescreen plus membrane. The template for the probe was prepared by PCR using an ago2 cDNA fragment cloned in pGEMT-easy vector. The primers used for PCR amplification are available upon request. Probes were labeled using Random Primed DNA Labeling Kit (Roche) and P32-dCTP, and hybridized at 65°C in 500 mM Church phosphate buffer containing 7% SDS and 1 mM EDTA.

RISC formation assay

Drosophila embryo extract preparation and synthetic siRNA labelling and annealing were described previously [56]. Reactions used different dilutions of cell free extraxts of wild-type or dop1 mutant embryos, 5 nM of P32-end-labelled siRNA and 1x lysis buffer containing 10% v/v of glycerol in a total volume of 10 µl. Reactions were incubated for 30 min to allow silencing complex formation. Native gel electrophoresis for separation of silencing complexes was essentially as described previously [31]. The in vitro reaction mixtures were diluted with 10 µl of loading buffer (1x lysis buffer, 6% Ficoll 400), and part of the sample was analyzed on a 3.9% (39:1 acrylamide-bisacrylamide) native acrylamide gel in 1xTBE buffer. The gels were dried and exposed to a storage phosphor screen.

Ago2 sequence comparisons

For various species, Ago2 family members were identified by searching FlyBase annotations or GenBank entries. For Ago2 proteins from Drosophila species, most candidates showed a glutamine-rich NTD. For those candidates that did not, we examined the eight distinct gene prediction algorithms from which the FlyBase consensus prediction is derived [40]. In several additional cases, at least one of these algorithms predicted a glutamine-rich NTD (details provided in Fig. S4). DUF1785, PAZ and PIWI domains were estimated using the Conserved Domain Search at NCBI. To estimate the extent of the NTD, the candidates were aligned with human Ago2 using the “Align two sequences by using BLAST” function at NCBI; the NTD was defined as those sequences amino-terminal to where significant alignment was detected. Similar results are obtained when candidates are aligned to any of the other human Argonaute family members (not shown). For human Ago2, the NTD was defined by aligning to D. melanogaster Ago2. For the phylogram in Fig. 7, we conducted multiple alignment of the protein sequences, neighbor-joining tree building and 1000 bootstrap trials via CLUSTALX. In similar phylograms based on all Drosophila Argonaute family members (not shown), the branch lengths for Ago2s are much longer than for Ago1s, consistent with the observation that Ago2 evolves much more rapidly than Ago1 [36]. These increased branch lengths hold true even if the NTD sequences of Ago2 are omitted from the analysis.

Supporting Information

Figure S1.

Amino acid sequence of GRR2 repeats in various D. melanogaster strains. GRR2 repeats display slight sequence variations, indicated by different colors. Fly strains differ both in number and type of repeat. The 3CPA122 pattern is identical to the one in the current FlyBase annotation for Ago2, and was also found in strains In(1)AB, w-14 melbourne, red e, and dop46. Note that the same overall repeat copy number can be achieved via distinct primary sequences (compare left and right columns below). This variability in sequence likely results in even greater number of distinct haplotypes, and the ten haplotypes in Table 1, which are based solely on repeat copy number, probably underestimate the true variability among the 32 strains surveyed.



Figure S2.

Variability in the Ago2 NTD for Drosophila simulans , mauritiana , and sechellia strains. The genomic DNA corresponding to exon 3 of ago2 was sequenced in a number of strains of the D. simulans species complex. The amino acid sequences for the corresponding NTD stretches were compared. A) Nine D. simulans and one D. mauritiana strain displayed highly similar sequences that could easily be aligned. Details on these strains are given in materials and methods. A total of six different haplotypes differ from each other by small insertions and deletions as well as single amino-acid changes. Strains sim2 and sim3 had the same sequence as strain Oxnard; strains maz1 and C167.4 had the same sequence as maz6. B) Comparison of D. simulans (strain maz6 is shown) and D. sechellia (two strains analyzed) sequences shows that they are composed of highly related stretches (indicated in red, green, and yellow) whose overall arrangement differs. In D. simulans, there is an imperfect, tandem repeat of the red + green + yellow stretches (118 or 121 aa long). In D. sechellia, a single copy of the red stretch is followed by three repeats (15 aa long) of the green stretch, and then one copy of the yellow stretch.



Figure S3.

Ago2 from Drosophila melanogaster , simulans and sechellia are dramatically variable in the NTD, but highly similar in the rest of the protein. Ago2 from D. melanogaster, simulans and sechellia aligned with CLUSTALW. Color code for domains as in Fig. S4.



Figure S4.

Sequences of Ago2 family members in insects and in Daphnia pulex For various species, Ago2 family members were identified by searching FlyBase annotations or GenBank entries. In a few cases, predicted proteins were corrected based on cDNA data or after resequencing problematic genomic regions; if alternative predictions for the protein included a glutamine- rich NTD, those predictions are listed below.In these sequences, four domains were identified: NTD (light blue), DUF1785 (pink), PAZ (green) and Piwi (yellow). The latter three domains were estimated using the Conserved Domain Search at NCBI. The extent of the NTD was based on comparison to human Ago2 (see Materials and Methods). Glutamine residues are highlighted in red and bold. For D. pseudoobscura, D. persimilis, and D. willistoni, FlyBase annotations suggest the existence of multiple Ago2 paralogs. Sequences of these putative paralogs were compared to ensure that they did not represent alternative isoforms of the same gene. For annotations that showed only minor differences from each other, only one such annotation was included in the list below. The phylogram in Fig. 7 suggests that the thus chosen candidates represent bona fide paralogs. Dsim\Ago2 Drosophila simulans NTD sequence based on our cDNA sequencing; rest of sequence based on Genbank entry EDX10559.1. The FlyBase annotation for this gene (GD14553) is largely identical across the NTD, DUF and PAZ domains, but predicts a deletion of much of the Piwi domain. Dsec\Ago2 Drosophila sechellia NTD sequence based on our cDNA sequencing; rest of sequence based on combining FlyBase annotations GM25537 and GM25538 and resequencing the genomic DNA between those annotations. Dere\Ago2 Drosophila erecta Based on alternative GNOMON prediction for FlyBase annotation GG15907. Dyak\Ago2 Drosophila yakuba FlyBase annotation GE22249. Dana\Ago2 Drosophila ananassae FlyBase annotation GF10056. Dpse\Ago2a Drosophila pseudoobscura FlyBase annotation GA28114. Note: because this prediction does not start with a Methionine, future analysis will likely refine the translation start site. Dpse\Ago2b Drosophila pseudoobscura FlyBase annotation GA27454. Dpse\Ago2c Drosophila pseudoobscura FlyBase annotation GA27411. Dpse\Ago2d Drosophila pseudoobscura Based on alternative GNOMON prediction for FlyBase annotation GA23629. Dpse\Ago2e Drosophila pseudoobscura FlyBase annotation GA26008. Dper\Ago2a Drosophila persimilis FlyBase annotation GL14308. Dper\Ago2b Drosophila persimilis FlyBase annotation GL21510. Dper\Ago2c Drosophila persimilis Based on alternative N-SCAN prediction for FlyBase annotation GL22202. Dper\Ago2d Drosophila persimilis FlyBase annotation GL24877. Dper\Ago2e Drosophila persimilis Flybase annotation GL19556. Dwil\Ago2a Drosophila willistoni FlyBase annotation GK10600. Dwil\Ago2b Drosophila willistoni FlyBase annotation GK24525. Dmoj\Ago2 Drosophila mojavensis FlyBase annotation GI13119. Dgri\Ago2 Drosophila grimshawi FlyBase annotation GH14741. Dvir\Ago2 Drosophila virilis Based on alternative N-SCAN prediction for FlyBase annotation GJ17143. Cqu\Ago2-1 Culex quinquefasciatus (Southern house mosquito) GenBank entry XP_001865113. Cqu\Ago2-2 Culex quinquefasciatus (Southern house mosquito) GenBank entry EDS33578.1. Aae\Ago2 Aedes aegypti (yellow fewer mosquito) GenBank entry ACR56327.1. Amel\Ago2 Apis mellifera (honey bee) GenBank entry XP_395048. Nvit\Ago2 Nasonia vitripennis (jewel wasp) GenBank entry XP_001607164.1. Bmor\Ago2 Bombyx mori (domestic silkworm) GenBank entry NP_001036995. Tcas\Ago2a Tribolium castaneum (red flour beetle) GenBank entry NP_001107842 (Argonaute-2a). Tcas\Ago2b Tribolium castaneum (red flour beetle) GenBank entry NP_001107828 (Argonaute-2b). Apis\Ago2 Acyrthosiphon pisum (pea aphid) GenBank entry XP_001944852.1. Phum\Ago2 Pediculus humanus (human louse) GenBank entry EEB09910. Dpul\Ago2 Daphnia pulex (common water flea) One of two alternative predictions on WfleaBase: DP_DGIL_SNO_00003046. Hsap\Ago2 Homo sapiens GenBank entry NP_036286.2.



Figure S5.

Comparison of Dpse\Ago2c and Dper\Ago2c. Dpse\Ago2c and Dper\Ago2c were aligned by CLUSTALW. The two proteins are almost completely identical through the entire coding region. The major differences are in the center of the NTD, where alignment is spotty, suggesting rapid changes in primary sequence. Color code for domains as in Fig. S4.



Table S1.

Evidence for expression of Ago2 NTDs in various insect species. For various insect Ago2s, the genomic regions corresponding to the NTD are indeed transcribed. Evidence includes cDNA analysis of Ago2 specifically, EST data from high-throughput sequencing efforts, and RNAseq data. If the transcribed region encompasses the entire NTD, this is indicated as “full” in the table.




We thank the Drosophila stock centers in Bloomington (Indiana, USA), Tuscon (Arizona, USA) and the Developmental Studies Hybridoma Bank (Iowa, USA) and H. Hollocher, B. Lazzaro, and L. Griffith for fly stocks and antibodies, respectively. We thank T. Volkmann, R. Webster, N. Levin and N. Rizzo for expert technical assistance, and Y. Guo and D.-H. Kim for help with cDNA cloning.

Author Contributions

Conceived and designed the experiments: DH BRB KO HS GH ECL MAW HAM. Performed the experiments: DH BRB KO TC WM ZJ JB MAW. Analyzed the data: DH BRB KO TC ZJ HS GH ECL MAW HAM. Contributed reagents/materials/analysis tools: BRB KO HS MAW HAM. Wrote the paper: BRB GH ECL MAW HAM.


  1. 1. Hutvagner G, Simard MJ (2008) Argonaute proteins: key players in RNA silencing. Nat Rev Mol Cell Biol 9: 22–32.
  2. 2. Farazi TA, Juranek SA, Tuschl T (2008) The growing catalog of small RNAs and their association with distinct Argonaute/Piwi family members. Development 135: 1201–1214.
  3. 3. Yigit E, Batista PJ, Bei Y, Pang KM, Chen CC, et al. (2006) Analysis of the C. elegans Argonaute family reveals that distinct Argonautes act sequentially during RNAi. Cell 127: 747–757.
  4. 4. Peters L, Meister G (2007) Argonaute proteins: mediators of RNA silencing. Mol Cell 26: 611–623.
  5. 5. Stefani G, Slack FJ (2008) Small non-coding RNAs in animal development. Nat Rev Mol Cell Biol 9: 219–230.
  6. 6. Ding SW, Li H, Lu R, Li F, Li WX (2004) RNA silencing: a conserved antiviral immunity of plants and animals. Virus Res 102: 109–115.
  7. 7. van Rij RP, Saleh MC, Berry B, Foo C, Houk A, et al. (2006) The RNA silencing endonuclease Argonaute 2 mediates specific antiviral immunity in Drosophila melanogaster. Genes Dev 20: 2985–2995.
  8. 8. Galiana-Arnoux D, Dostert C, Schneemann A, Hoffmann JA, Imler JL (2006) Essential function in vivo for Dicer-2 in host defense against RNA viruses in drosophila. Nat Immunol 7: 590–597.
  9. 9. Wang XH, Aliyari R, Li WX, Li HW, Kim K, et al. (2006) RNA interference directs innate immunity against viruses in adult Drosophila. Science 312: 452–454.
  10. 10. Hammond SM, Boettcher S, Caudy AA, Kobayashi R, Hannon GJ (2001) Argonaute2, a link between genetic and biochemical analyses of RNAi. Science 293: 1146–1150.
  11. 11. Okamura K, Ishizuka A, Siomi H, Siomi MC (2004) Distinct roles for Argonaute proteins in small RNA-directed RNA cleavage pathways. Genes Dev 18: 1655–1666.
  12. 12. Rand TA, Ginalski K, Grishin NV, Wang X (2004) Biochemical identification of Argonaute 2 as the sole protein required for RNA-induced silencing complex activity. Proc Natl Acad Sci U S A 101: 14385–14389.
  13. 13. Williams RW, Rubin GM (2002) ARGONAUTE1 is required for efficient RNA interference in Drosophila embryos. Proc Natl Acad Sci U S A 99: 6889–6894.
  14. 14. Forstemann K, Tomari Y, Du T, Vagin VV, Denli AM, et al. (2005) Normal microRNA maturation and germ-line stem cell maintenance requires Loquacious, a double-stranded RNA-binding domain protein. PLoS Biol 3: e236.
  15. 15. Okamura K, Lai EC (2008) Endogenous small interfering RNAs in animals. Nat Rev Mol Cell Biol 9: 673–678.
  16. 16. Meyer WJ, Schreiber S, Guo Y, Volkmann T, Welte MA, et al. (2006) Overlapping functions of argonaute proteins in patterning and morphogenesis of Drosophila embryos. PLoS Genet 2: e134.
  17. 17. Murphy D, Dancis B, Brown JR (2008) The evolution of core proteins involved in microRNA biogenesis. BMC Evol Biol 8: 92.
  18. 18. Xu K, Bogert BA, Li W, Su K, Lee A, et al. (2004) The fragile X-related gene affects the crawling behavior of Drosophila larvae by regulating the mRNA level of the DEG/ENaC protein pickpocket1. Curr Biol 14: 1025–1034.
  19. 19. Liu Y, Ye X, Jiang F, Liang C, Chen D, et al. (2009) C3PO, an endoribonuclease that promotes RNAi by facilitating RISC activation. Science 325: 750–753.
  20. 20. Fagegaltier D, Bouge AL, Berry B, Poisot E, Sismeiro O, et al. (2009) The endogenous siRNA pathway is involved in heterochromatin formation in Drosophila. Proc Natl Acad Sci U S A 106: 21258–21263.
  21. 21. Pepper AS, Beerman RW, Bhogal B, Jongens TA (2009) Argonaute2 suppresses Drosophila fragile X expression preventing neurogenesis and oogenesis defects. PLoS One 4: e7618.
  22. 22. Deshpande G, Calhoun G, Schedl P (2005) Drosophila argonaute-2 is required early in embryogenesis for the assembly of centric/centromeric heterochromatin, nuclear division, nuclear migration, and germ-cell formation. Genes Dev 19: 1680–1685.
  23. 23. Ghildiyal M, Seitz H, Horwich MD, Li C, Du T, et al. (2008) Endogenous siRNAs derived from transposons and mRNAs in Drosophila somatic cells. Science 320: 1077–1081.
  24. 24. Czech B, Malone CD, Zhou R, Stark A, Schlingeheyde C, et al. (2008) An endogenous small interfering RNA pathway in Drosophila. Nature 453: 798–802.
  25. 25. Okamura K, Chung WJ, Ruby JG, Guo H, Bartel DP, et al. (2008) The Drosophila hairpin RNA pathway generates endogenous short interfering RNAs. Nature 453: 803–806.
  26. 26. Kawamura Y, Saito K, Kin T, Ono Y, Asai K, et al. (2008) Drosophila endogenous small RNAs bind to Argonaute 2 in somatic cells. Nature 453: 793–797.
  27. 27. Chung WJ, Okamura K, Martin R, Lai EC (2008) Endogenous RNA interference provides a somatic defense against Drosophila transposons. Curr Biol 18: 795–802.
  28. 28. Okamura K, Balla S, Martin R, Liu N, Lai EC (2008) Two distinct mechanisms generate endogenous siRNAs from bidirectional transcription in Drosophila melanogaster. Nat Struct Mol Biol 15: 998.
  29. 29. Meister G, Landthaler M, Patkaniowska A, Dorsett Y, Teng G, et al. (2004) Human Argonaute2 mediates RNA cleavage targeted by miRNAs and siRNAs. Mol Cell 15: 185–197.
  30. 30. Liu J, Carmell MA, Rivas FV, Marsden CG, Thomson JM, et al. (2004) Argonaute2 is the catalytic engine of mammalian RNAi. Science 305: 1437–1441.
  31. 31. Pham JW, Pellino JL, Lee YS, Carthew RW, Sontheimer EJ (2004) A Dicer-2-dependent 80s complex cleaves targeted mRNAs during RNAi in Drosophila. Cell 117: 83–94.
  32. 32. Lazzaro BP, Clark AG (2001) Evidence for recurrent paralogous gene conversion and exceptional allelic divergence in the Attacin genes of Drosophila melanogaster. Genetics 159: 659–671.
  33. 33. Tompa P (2003) Intrinsically unstructured proteins evolve by repeat expansion. Bioessays 25: 847–855.
  34. 34. Lachaise D, David J, Lemeunier F, Tsacas L, Ashburner M (1986) The reproductive relationships of Drosophila sechellia with D. mauitiana, D. simulans, and D. melanogaster from the Afro-tropical region. Evolution 40: 262–271.
  35. 35. Bettencourt BR, Hogan CC, Nimali M, Drohan BW (2008) Inducible and constitutive heat shock gene expression responds to modification of Hsp70 copy number in Drosophila melanogaster but does not compensate for loss of thermotolerance in Hsp70 null flies. BMC Biol 6: 5.
  36. 36. Obbard DJ, Jiggins FM, Halligan DL, Little TJ (2006) Natural selection drives extremely rapid evolution in antiviral RNAi genes. Curr Biol 16: 580–585.
  37. 37. Obbard DJ, Welch JJ, Kim KW, Jiggins FM (2009) Quantifying adaptive evolution in the Drosophila immune system. PLoS Genet 5: e1000698.
  38. 38. Begun DJ, Holloway AK, Stevens K, Hillier LW, Poh YP, et al. (2007) Population genomics: whole-genome analysis of polymorphism and divergence in Drosophila simulans. PLoS Biol 5: e310.
  39. 39. Eisen M (2007) Assembly/Alignement/Annotation of 12 related Drosophila species.
  40. 40. Clark AG, Eisen MB, Smith DR, Bergman CM, Oliver B, et al. (2007) Evolution of genes and genomes on the Drosophila phylogeny. Nature 450: 203–218.
  41. 41. Campbell CL, Black WCt, Hess AM, Foy BD (2008) Comparative genomics of small RNA regulatory pathway components in vector mosquitoes. BMC Genomics 9: 425.
  42. 42. Tomoyasu Y, Miller SC, Tomita S, Schoppmeier M, Grossmann D, et al. (2008) Exploring systemic RNA interference in insects: a genome-wide survey for RNAi genes in Tribolium. Genome Biol 9: R10.
  43. 43. Wang RL, Wakeley J, Hey J (1997) Gene flow and natural selection in the origin of Drosophila pseudoobscura and close relatives. Genetics 147: 1091–1106.
  44. 44. Bettencourt BR, Hogan CC, Nimali M (2007) Polyglutamine expansion in Drosophila: thermal stress and Hsp70 as selective agents. J Biosci 32: 537–547.
  45. 45. Sawyer LA, Hennessy JM, Peixoto AA, Rosato E, Parkinson H, et al. (1997) Natural variation in a Drosophila clock gene and temperature compensation. Science 278: 2117–2120.
  46. 46. Sawyer LA, Sandrelli F, Pasetto C, Peixoto AA, Rosato E, et al. (2006) The period gene Thr-Gly polymorphism in Australian and African Drosophila melanogaster populations: implications for selection. Genetics 174: 465–480.
  47. 47. Shi H, Djikeng A, Tschudi C, Ullu E (2004) Argonaute protein in the early divergent eukaryote Trypanosoma brucei: control of small interfering RNA accumulation and retroposon transcript abundance. Mol Cell Biol 24: 420–427.
  48. 48. Shi H, Chamond N, Djikeng A, Tschudi C, Ullu E (2009) RNA interference in Trypanosoma brucei: role of the n-terminal RGG domain and the polyribosome association of argonaute. J Biol Chem 284: 36511–36520.
  49. 49. Yang ZR, Thomson R, McNeil P, Esnouf RM (2005) RONN: the bio-basis function neural network technique applied to the detection of natively disordered regions in proteins. Bioinformatics 21: 3369–3376.
  50. 50. Dunker AK, Brown CJ, Lawson JD, Iakoucheva LM, Obradovic Z (2002) Intrinsic disorder and protein function. Biochemistry 41: 6573–6582.
  51. 51. Liu JJ, Lindquist S (1999) Oligopeptide-repeat expansions modulate ‘protein-only’ inheritance in yeast. Nature 400: 573–576.
  52. 52. Parham SN, Resende CG, Tuite MF (2001) Oligopeptide repeats in the yeast protein Sup35p stabilize intermolecular prion interactions. EMBO J 20: 2111–2119.
  53. 53. Sainz A, Wilder JA, Wolf M, Hollocher H (2003) Drosophila melanogaster and D. simulans rescue strains produce fit offspring, despite divergent centromere-specific histone alleles. Heredity 91: 28–35.
  54. 54. Müller HA, Wieschaus E (1996) armadillo, bazooka, and stardust are critical for early stages in formation of the zonula adherens and maintenance of the polarized blastoderm epithelium in Drosophila. J Cell Biol 134: 149–163.
  55. 55. Riggleman B, Schedl P, Wieschaus E (1990) Spatial expression of the Drosophila segment polarity gene armadillo is posttranscriptionally regulated by wingless. Cell 63: 549–560.
  56. 56. Haley B, Tang G, Zamore PD (2003) In vitro analysis of RNA interference in Drosophila melanogaster. Methods 30: 330–336.
  57. 57. Welte MA, Gross SP, Postner M, Block SM, Wieschaus EF (1998) Developmental regulation of vesicle transport in Drosophila embryos: forces and kinetics. Cell 92: 547–557.