Figures
Abstract
Pallister Killian syndrome (OMIM: # 601803) is a rare multisystem disorder typically caused by tissue limited mosaic tetrasomy of chromosome 12p (isochromosome 12p). The clinical manifestations of Pallister Killian syndrome are variable with the most common findings including craniofacial dysmorphia, hypotonia, cognitive impairment, hearing loss, skin pigmentary differences and epilepsy. Isochromosome 12p is identified primarily in skin fibroblast cultures and in chorionic villus and amniotic fluid cell samples and may be identified in blood lymphocytes during the neonatal and early childhood period. We performed genomic expression profiling correlated with interphase fluorescent in situ hybridization and single nucleotide polymorphism array quantification of degree of mosaicism in fibroblasts from 17 Caucasian probands with Pallister Killian syndrome and 9 healthy age, gender and ethnicity matched controls. We identified a characteristic profile of 354 (180 up- and 174 down-regulated) differentially expressed genes in Pallister Killian syndrome probands and supportive evidence for a Pallister Killian syndrome critical region on 12p13.31. The differentially expressed genes were enriched for developmentally important genes such as homeobox genes. Among the differentially expressed genes, we identified several genes whose misexpression may be associated with the clinical phenotype of Pallister Killian syndrome such as downregulation of ZFPM2, GATA6 and SOX9, and overexpression of IGFBP2.
Citation: Kaur M, Izumi K, Wilkens AB, Chatfield KC, Spinner NB, Conlin LK, et al. (2014) Genome-Wide Expression Analysis in Fibroblast Cell Lines from Probands with Pallister Killian Syndrome. PLoS ONE 9(10): e108853. https://doi.org/10.1371/journal.pone.0108853
Editor: Ken Mills, Queen's University Belfast, United Kingdom
Received: May 23, 2014; Accepted: August 26, 2014; Published: October 16, 2014
Copyright: © 2014 Kaur et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: The authors confirm that all data underlying the findings are fully available without restriction. All relevant data are within the paper and its Supporting Information files.
Funding: This research was supported by the Children's Hospital of Philadelphia Institutional Development Fund (IDK). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Originally described by Pallister et al. [1], [2] and later by Killian and Teschler-Nicola, Pallister Killian Syndrome (PKS) (OMIM #601803) also known as tetrasomy 12p and isochromosome 12p mosaicism is a rare chromosomal aneuploidy with an estimated prevalence of 1/20,000 [3], [4]. PKS is characterized by tissue-specific mosaicism of a supernumerary isochromosome which is typically a metacentric chromosome composed of material from the short arm of chromosome 12: i(12)(p10) [5]. Most commonly, individuals with PKS have four copies of the complete short arm of chromosome 12, although rarely, probands may have a complete or partial duplication of 12p and still manifest the full PKS phenotype [6]. We have recently defined a PKS minimal critical region mapping to 12p13.31 [7]. There have been more than 150 reported probands (reviewed in Wilkens et al.) [8], [9]. Probands manifest a very recognizable pattern of malformations however there is a wide range of variability in phenotypic expression (Figure 1). Typical features include cognitive impairment, prenatal overgrowth followed by postnatal growth deceleration, hypotonia, seizures, cutaneous hypo and/or hyperpigmentation, facial dysmorphia including a high forehead, broad nasal bridge, telecanthus, sparse fronto-temporal hair at birth, high arched or cleft palate, posterior helical ear pits, short neck, supernumerary nipples, limb and genitourinary anomalies, congenital heart defects and diaphragmatic hernias [9].
(A)–(D). Full face and profile views of the facial features in two unrelated children with PKS. (E)–(G). Swirly hypo- and hyperpigmentation of the skin in 3 children with PKS. (H)–(J). Broad first toes in 3 children with PKS.
Isochromosome 12p is seen mainly in skin fibroblast cultures and in chorionic villus and amniotic fluid cell samples but can be identified in blood lymphocytes during the neonatal and early childhood period [10], [11]. The isochromosome is often lost in the peripheral blood, presumably due to a selective growth advantage of the karyotypically normal disomic cell populations in the bone marrow of PKS individuals [12]. The percentage of tetrasomic cells does not correlate with severity of the syndrome, the patient's longevity, or degree of mental retardation [9], [13], [14]. The prevalence of cells with an extra metacentric chromosome i(12)(p10) is usually highly variable and tissue-limited or tissue-specific mosaicism is a well-described characteristic of PKS. Diagnosis of PKS, especially in those individuals beyond the neonatal period, traditionally requires a skin biopsy and analysis of fibroblasts.
The constellation of structural and neurocognitive deficits seen in PKS in a highly conserved manner, coupled with a narrow minimal critical region delineated on 12p13.31 would suggest that a few genes (or even a single gene) within this region that are critical regulators of human development are responsible for the PKS phenotype when present in extra copies. In order to effect the pleiotropic manifestations observed in PKS the critical gene(s) on 12p are likely to be key regulators of downstream genes or gene networks important for the growth and differentiation of the tissues affected in this diagnosis. In order to begin to delineate the downstream 12p effector genes in PKS we used the Affymetrix Human Genome U133 plus 2.0 arrays to perform a genome-wide expression analysis in 17 probands with PKS and 9 age, gender and race matched controls. This analysis was able to identify 354 genes that were statistically differentially expressed in PKS probands, 180 of which were up- and 174 down-regulated with at least a 1.5 fold change and a p value less than 0.05. The most statistically significantly dysregulated genes on 12p mapped to 12p13.31, a region previously described cytogenetically to represent a PKS minimal critical region [7]. The non-12p genes that were most significantly dysregulated include a large number of homeobox genes and other transcription factors critical in mammalian development.
Materials and Methods
Study population
Fibroblast cell lines from a cohort of 17 probands (5 females and 12 males) with PKS and 9 age, gender and race matched normal controls (5 females and 4 males) were used (Table 1). The control fibroblast cell lines were obtained from the Coriell Cell Repository (http://ccr.coriell.org/). All patients and families enrolled in this study were done so in writing by following a specific approval for this study from the Institutional Review Board at The Children's Hospital of Philadelphia by the Committee for the Protection of Human Subjects (approval # IRB 10-007476, DHHS Federal Wide Assurance Identifier: FWA0000459). For minors and those individuals unable to consent themselves due to intellectual disability their guardians or appointed caretakers provided consent. Consents were obtained in writing for the publication of photographs of individuals depicted in the figure. One or more experienced clinical dysmorphologists evaluated all the affected individuals. Sample processing was performed in two batches, batch I comprised 8 patients and 5 controls and batch II had 9 patients and 4 controls.
Cell culture
Fibroblasts cell lines from 17 probands with PKS and nine normal controls were uniformly cultured in RPMI 1640 (Life Technologies, Carlsbad, CA, USA) supplemented with 20% FBS (Hyclone South Logan, UT, USA), antibiotics (100 units/ml of penicillin and 100 ug/ml of streptomycin), and 1% L-glutamine (Life Technologies, Carlsbad, CA, USA). Approximately 9.0–15.0×105 exponentially growing cells were seeded in 15 ml media in 75 ml falcon flasks (BD Biosciences, San Jose, CA, USA). Cells were incubated at 37°C in a humidified atmosphere of 5% CO2. Cells were trypsinized (0.25% trypsin-EDTA) and split at 75–80% confluency. All 26-cell lines were cultured until they reached a population-doubling level between 15–35. Total RNA, and DNA were isolated from the same cultures for all the samples. Slides were also prepared for cytogenetic analyses from the same cultures. Standard G-banded karyotyping, single nucleotide polymorphism (SNP) array, and fluorescent in situ hybridization (FISH) analysis of 12p was performed on all cell lines at the start and end points of culturing to provide an accurate estimate of degree of mosaicism of these samples (Table 1).
Cytogenetic analysis
Chromosome preparations from cultured fibroblasts were analyzed by FISH using a chromosome 12p specific DNA probe. The probe was labeled by nick translation with spectrum green. FISH was done according to standard protocol [15]. To validate the level of mosaicism in the probands 2 ml of cell culture from the flasks used for RNA and DNA isolation were cultured on flaskettes (Thermo scientific, Waltham, MA, USA). Slides were prepared for chromosome (interphase) analysis using standard cytogenetic protocols. For each proband 200 cells were analyzed.
We also used genome-wide single nucleotide polymorphism (SNP) arrays (Illumina HumanHap 550K; Illumina, San Diego, CA, USA) to detect percentage of mosaicism in all seventeen probands with PKS as described previously [12]. For this analysis DNA was isolated from the cultured fibroblasts (OD260/OD280 1.8–2.0 and OD260/OD230>2.0, respectively). The samples were genotyped on the Illumina Bead Station (Illumina, San Diego, CA, USA). Analysis of all copy number variation calls was detected using Illumina Bead Studio software. The degree of mosaicism in all the probands were detected by assessing probe intensities measured by log R ratios, along with shifts in genotype frequencies of SNP probes measured by B allele frequencies [16].
RNA isolation and sample preparation for hybridization
Total RNA was isolated from each sample using Qiagen RNeasy mini kit (Qiagen, Valencia, CA, USA). All RNA samples exhibited intact 28S and 18S ribosomal RNA on denaturing agarose gel electrophoresis and OD260/OD280 absorbance ratio fell within the acceptable range of 1.8–2.1. RNA yield was determined spectrophotometrically (Nanodrop ND-1000 spectrophotometer; Thermo scientific, Waltham, MA, USA). RNA extracts were DNase treated. For array analysis at least 3 ug of total RNA was transcribed into Double Stranded cDNA with oligo (dT)24 T7 primer using Invitrogen SuperScript Double-Stranded cDNA synthesis kit (Life Technologies, Grand Island, NY, USA). The cDNA was purified with Affymetrix GeneChip Sample Cleanup module (Affymetrix, Santa Clara, CA, USA) and used into an in vitro transcription reaction to produce labeled cRNA with Enzo Bioarray High Yield RNA Transcript Labeling Kit from Enzo Life Sciences (Farmingdale, NY, USA) and further fragmented to 35–200 bp oligos for hybridization. All steps for sample preparation and processing were performed according to manufacturer's instructions.
Hybridization to Affymetrix GeneChip expression array and data collection
The newly synthesized and biotin labeled cRNA was fragmented by incubation in fragmentation buffer for 35 minutes at 94°C, 15 ug/30 ul of the fragmented samples were sent to the microarray facility at The Children's Hospital of Philadelphia for hybridization. Microarray hybridization was performed on commercially available high density Affymetrix HG-U133 plus 2.0 GeneChip arrays (Affymetrix, Santa Clara, CA, USA). Arrays were washed and stained according to standard affymetrix protocols using an Affymetrix Fluidics Workstation. Arrays were scanned using Affymetrix GeneArray scanner 3000 and the cell intensities (.CEL files) were captured by Affymetrix Genechip Operating Software (GCOS) as per the Affymetrix protocol. The HG U133 Plus 2.0 Arrays contains over 54,000 probe sets to analyze the expression level of more than 47,000 transcripts and variants, including approximately 38,500 well-characterized human genes. The sequences from which these probes were derived were selected from GeneBank, dnEST, and Refseq [17].
Data analysis
All Affymetrix probes were re-grouped into unique Entrez gene IDs using custom library file downloaded from BRAINARRAY database (http://brainarray.mbni.med.umich.edu). The raw data in.CEL files were normalized and summarized by robust multiarray average (RMA) method to generate a 26*17,726 matrix, where 17,726 is the number of unique Entrez genes and 26 is the number of samples. The normalized data were then log2-transformed.
The normalized data was subsequently analyzed by the unsupervised multivariate analysis tool, principal component analysis (PCA). Differential expression of genes between control and PKS samples was evaluated by the difference of group means (magnitude of change) and the p value of t test (significance of change).
Gene functional annotation and clustering analysis
To identify biologically relevant groups of genes we performed functional gene annotation and cluster analysis using the Database for Annotation, Visualization and Integrated Discovery (DAVID) of up- and down-regulated genes (http://david.abcc.ncifcrf.). To investigate the biological functions involved in the discriminating genes we did Gene Ontology (GO) Analysis (http://www.geneontology.org). Using Non-stringent cutoffs (25% difference) and p values less than 0.05, pathway analysis was performed using Ingenuity Pathway Analysis (IPA) (Ingenuity Systems, Inc., http://www.ingenuity.com). IPA uses the knowledge base to identify interactions of input genes within the context of known biological pathways.
Results
Cytogenetic analysis
Levels of mosaicism of the PKS probands used in this study ranged from 0% to 100% of cells. In two samples the isochromosome could not be detected, two had a very low level of 4% and 8% and in the rest had mosaic levels ranging from 40% to 100% at the time of RNA extraction for the expression arrays (Table 1).
Gene expression pattern in PKS
To test whether the probands with PKS have a unique and specific gene expression profile, we used clustering and principal component analysis. Figure 2A shows the unsupervised clustering of all 26 samples using all genes. Control and PKS samples were not distinctively separated. Gender is suggested as a confounding factor according to a large cluster of male samples clustering in the middle. Clustering of samples using expressed genes located only on 12p allowed for a more clear separation of control and PKS samples (Figure 2B). The difference among the probands likely reflects their different levels of mosaicism. Gender is an even more important factor, especially for the control samples (Figure 2B). We further explored the gene expression profile using PCA. By visualizing projections of the components identified by PCA in low dimension spaces, we were able to observe the grouping of PKS and control samples reflecting underlying patterns in their gene expression profiles (Figure 2C, Table S5). Variability among the probands likely depicts the different levels of mosaicism.
Red squares/circles represent PKS patients and Green squares/circles represent control samples. (A) Unsupervised clustering of 26 samples using all genes. (B) Unsupervised clustering of 26 samples using genes located on 12p.(C) PCA result. Proportion of Variance % (PC1-24.818, p 0.001; PC2-17.814, p 0.022; PC3-0.022, p 0.772).
Expression/level of mosacism
To identify if any correlations existed between the expression levels of the genes on the short arm of 12 to the level of mosaicism, we compared the copy number of genes on 12p to expression level between the patients and the controls (Figure 3a). The data suggests that as long as the 12p genes are commonly expressed in healthy control samples, their expression level in patients is proportional to the level of mosaic (Figure 3b). The average expression level of 12p genes and the level of mosaicism had a Pearson's correlation of r = 0.972 (p = 5.0E-14).
a: Mosaic 12p expression level correlation: Average expression of 171 genes on 12p in patients and controls. Red bars are patients and Grey is controls. X-axis represents samples and Y-axis shows average expression of genes on 12p. b: Level of i12p mosaicism compared to 12p gene expression: average of 64 genes with expression higher than the 3rd quartile of global expression distribution, were correlated to mosaicism%. The blue line in the figure is the fitting line of linear regression. Red diamonds are the probands and green are the controls.
Differentially expressed genes between PKS and control groups
As a next step, we undertook the identification of genes whose expression levels are significantly different between the PKS and control groups. In general, there were a small number of genes whose expression was noticeably changed in PKS. Using non-stringent cutoffs (at 25% difference and p less than 0.05), only 354 genes (2% of genes analyzed) were differentially expressed between the two groups, 180 genes were up- and 174 genes down regulated in probands with PKS (Table S1 and S2). Up-regulated genes were highly enriched with genes located on the short arm of chromosome 12 (12p), fitting the pathology of PKS. Out of 180 up-regulated genes, 57 (32%) were located on 12p. Amongst these, genes mapping to cytogenetic band 12p13.31 were among the ones that were most significantly dysregulated in the probands compared to controls. Out of approximately 100 genes in this region, CLEC2B, LOC374443 and NCAPD2 were over-expressed by 1.5 fold in the PKS probands (Table 2). None of the down-regulated genes mapped to 12p. The magnitude of fold increase in the expression of the differentially expressed genes between the controls and the patients ranged from 0.3 to 2.4. A full list of differentially expressed genes is provided in Tables S1 and S2. These lists include many disease-associated genes, and ZFPM2 was the most significantly down regulated gene, GATA6 ranked 5th, and SOX9 was 24th. IGFBP2 was ranked second in the upregulated gene list.
Validation of expression array data by ddPCR
Using the QX100 Droplet Digital PCR system (Bio-Rad, Pleasanton, CA) expression levels of 10 significantly dysregulated genes, 5 up- and 5 down-regulated genes (Table S6) were validated. RNA expression levels from all samples were measured with commercially available FAM labeled TaqMan MGB probes (Applied Biosystems), standardized to VIC labeled TBP and HPRT TaqMan probes.
Droplet digital PCR workflow and data analysis
The ddPCR was performed using manufacturer's protocol (Bio-Rad Laboratories), 25 ul of ddPCR mix was prepared using 12.5 ul of Bio-Rad 2× Supermix, 1.25 ul of each of 20× primer/probe mix (Applied Biosystems) along with 60 ng of cDNA, 20 ul of reaction mix was then emulsified with 70 ul of oil using a QX-100 droplet generator according to the manufacturer's instructions (Bio-Rad, Hercules, CA), following PCR amplification droplets were quantified by QX100 droplet reader (Bio-Rad, Hercules, CA). QuantaSoft software version 1.5.38.111 (Bio-Rad, Hercules, CA) was used to quantify the copies/µl of each queried target per well. All samples were run in duplicate for all 10 assays. The gene expression levels measured by ddPCR correlated well with the result of expression array data (Figure S1). The two sets of data had the Pearson's correlation coefficient of r = 0.95, p = 2.6E-5.
Biological pathways affected in PKS
Using DAVID and GO terms, we quarried for particular classes of genes or biological pathway significantly affected in PKS. The up-regulated genes identified using DAVID included Homeobox, antennepedia type, sequence specific DNA binding, transcription factor activity and genes involved in various developmental processes (Table S3 and S4). Ten out of 180 up-regulated genes were HOX/Homeobox genes, the majority of which were antennapedia- like homeobox- containing HOXB (B2, B3, B5, B6, B7) and MEOX2 genes along with the engrailed homeobox family gene EN1 and the zinc finger homeobox 1b ZEB2, mutations in which are associated with Mowat-Wilson syndrome [18].
The genes that are down-regulated by at least 1.5 fold in PKS includes genes involved in anatomical structural morphology and development, various developmental processes and system development and genes regulating signal transduction, cell morphology and cell communication (Table S3 and S4). Several homeobox genes were found to be downregulated. The downregulated homebox genes were mostly from the HOXA cluster (A1, A5, A11, A13). Homeobox genes LHX9 and MEIS2 were also down regulated in the patients as compared to the controls.
In humans HOX genes are found in 4 clusters (A, B, C and D). In probands with PKS, genes of cluster B were up regulated and cluster A was down regulated compared to the controls. Figure 4A is a Box plot of all 4 HOX gene clusters. Cluster C and D demonstrated no obvious change in expression level. Mammalian HOX gene clusters consist of 13 sets of paralogous group (group 1 to 13), and HOX genes belonging to the same paralogous group act synergistically. When we analyze the expression level based on paralogous groups, the central class HOX paralogous group especially paralogous group 6 and 7 were upregulated and abdominal B class HOX paralogous group, especially group 10 and 11 were downregulated throughout HOX cluster A to D (Figure 4B).
HOX A is down- and HOX B Cluster is up-regulated in PKS patients.
Genes were also classified according to their annotated role in biological processes, molecular function and cellular components from GO. Categories such as “development”, “metabolic processes”, “nucleic acid binding”, “gene expression”, “transcription”, “cellular processes and regulation of cell growth”, “cell communication and signal transduction” and “catalytic activities” all demonstrated a higher score.
Among the genes down-regulated the highest proportion corresponded to cell communication, signal transduction and cellular processes along with genes involved in development.
Functional analysis using IPA
The identified genes were analyzed using IPA to investigate functional networks and gene ontology. With the help of ingenuity we were able to establish a molecular link between 12p and the HOX genes (Figure 5). ATN1, a gene located on 12p13.31, is a transcriptional regulator and is the cause of the dominant neurological disorder dentatorubral pallidoluysian atrophy (DRPLA) when mutated [19], [20]. ATN1 is up regulated in PKS. It interacts with CREBBP, a master transcriptional regulator (and the cause of the developmental disorder Rubinstein-Taybi syndrome, when mutated) [21]. CREBBP itself does not demonstrate a significant expression change in PKS, however it interacts with the HOXB genes. The dysregulation of ATN1 may be affecting the dysregulation of the HOX genes through the actions of CREBBP although further work will be needed to confirm this.
Green circles represent the genes down-regulated in PKS probands, and red circles represent the genes up-regulated in PKS probands.
Discussion
PKS is a multisystem developmental disorder with a highly conserved phenotype. In this study, using the skin fibroblast cell lines derived from 17 probands with PKS, we demonstrate that PKS probands have a unique gene expression signature, which is characterized by misexpression of many developmentally critical genes including multiple homeobox genes. Since many genetic developmental disorders are caused by the perturbation of proper regulation of gene expression during embryogenesis, our observation of a highly conserved pattern of abnormal gene expression of many developmentally critical genes fits very well with the pleiotropic phenotype seen in PKS.
We have previously defined a PKS critical region, whose dosage gain leads to the PKS phenotype [7]. Interestingly, the same region of chromosome 12p, a small 2.80 Mb region on 12p13.31 with 26 genes was identified to contain the most significantly dysregulated gene expression in the PKS probands according to DAVID's analysis, supporting the key role this region likely plays in the pathogenesis of PKS. Out of approximately 100 genes localizing to 12p13.31, CLEC2B, LOC374443 and NCAPD2 were over-expressed by at least 1.5 fold in the PKS probands. Among these three genes, NCAPD2 is of particular interest. NCAPD2 encodes the condensin I complex subunit D2, and plays a well-documented role in regulating the gene expression [22]. Therefore, overexpression of NCAPD2 may play a central role in the global gene expression abnormality seen in PKS probands as a primary event due to the presence of the isochromosome 12p. In addition to these three genes, chromosomal region 12p13.31 contains additional interesting candidate genes, an extra copy of which could lead to the core phenotype of PKS, although the fold difference of the expression levels were not above 1.5. ING4 and CHD4 represent attractive candidate genes responsible for the pleiotropic phenotype seen in PKS, because of the known roles played by these genes in transcriptional regulation. ING4 encodes a tumor suppressor protein, and plays a role in DNA repair, chromatin remodeling, and regulation of cell growth [23], [24]. The expression level of ING4 was 1.26 fold higher in PKS probands. CHD4 is in the same gene family as CHD7 whose haploinsufficiency leads to CHARGE syndrome, which is a multisystem developmental disorder [25]. CHD4 is the main component of the nucleosome remodeling and deacetylase complex [26]. ATN1, which was highlighted by IPA, also resides at 12p13.31, and mutations of ATN1 leads to the neurodegenerative disorder DRPLA as discussed above.
The evolutionarily highly conserved HOX genes are a subgroup of the homeobox genes. The HOX genes are a set of transcription factor encoding genes that pattern the anterior-posterior body axis of animals. The 39 human HOX genes are located in four clusters (A–D) on different chromosomes and consists of 9 to 11 genes in each cluster, arranged in tandem that play important roles in embryonic pattering and cell differentiation [27]. The HOX B cluster is up- and HOXA cluster is down-regulated in the probands, while Cluster C and D had no obvious change in expression level. Such cluster specific changes may implicate the possibility of chromatin modification affecting the entire HOX gene cluster in the genome.
When HOX gene expression level was classified by paralogous group, interestingly, the central class HOX paralogous group especially paralogous group 6 and 7 were upregulated and abdominal B class HOX paralogous group, especially group 10 and 11, were downregulated throughout HOX cluster A to D. Since the central class of the HOX gene groups, and abdominal B class HOX groups, play roles in defining the body segmentation pattern of the thorax and limb, such a dysregulated expression may be associated with the skeletal phenotype of PKS such as vertebral bone/rib anomalies and brachydactyly [28].
Since the most dysregulated genes in PKS were enriched for homebox genes and genes located on 12p, a putative link between the two using IPA was identified. The ATN1 gene located on 12p interacts with CREBBP, a master transcriptional regulator, mutations in which are known to cause Rubinstein Taybi syndrome, no obvious change was noticed in the expression level of CREBBP in the probands' tissue studied (skin fibroblast). CREBBP also interacts with HOXB genes that are upregulated in the probands. It is possible that dysregulation of the ATN1 gene is affecting the HOXB genes modifying the activity of the CREBBP protein without affecting its mRNA level. Further studies need to be done to confirm this hypothesis.
MED21 was predicted to affect the HOXB genes via modulation of the CREBBP gene by IPA. MED21 encodes a member of the mediator complex subunit 21 family, and is involved in transcriptional regulation of RNA polymerase II transcribed genes [29]. The expression level of MED21 was elevated in PKS probands. Although MED21 localizes to 12p11.23, which is far from the newly defined PKS critical region, the involvement of MED21 in the pathogenesis of PKS requires further evaluation, given its critical role in transcriptional regulation.
The downregulated and upregulated genes identified in this expression study highlight many interesting genes whose misexpression may be associated with the PKS phenotype. The most significantly down regulated gene was ZFPM2 located on chromosome 8q23. Haploinsufficiency of ZFPM2 is associated with congenital diaphragmatic hernia (CDH) as well as congenital heart defects (CHD), both consistent features of PKS [30], [31]. GATA6, located on chromosome 18q11, was also demonstrated to be downregulated in PKS fibroblasts. Mutations of GATA6 are associated with various types of CHD, hence, GATA6 may also be associated with the pathogenesis of CHD in PKS [32]. Another gene whose misexpression may be directly related to the phenotype is SOX9, because mutations of SOX9 cause campomelic dysplasia characterized by limb shortening, micrognathia and cleft palate/Robin sequence and sex reversal, and there is phenotypic overlap between campomelic dysplasia and PKS [33], [34]. Therefore, it is tempting to speculate the role of SOX9 downregulation in the pathogenesis of cleft palate and limb shortening seen in PKS. IGFBP2 was significantly upregulated in PKS fibroblasts. We hypothesize that overexpression of IGFBP2 may be associated with the postnatal growth deceleration phenotype seen in PKS. IGFBP2 sequesters free IGF proteins, and functions to mitigate the IGF signaling pathway [35]. Mouse models of IGFBP2 overexpression demonstrate a postnatal growth retardation phenotype, which is similar to that seen in PKS probands [36].
DAVID annotation was helpful in deciphering which signaling pathways and biological functions are significantly affected in PKS. The terms associated with downregulated and upregulated genes suggests that the pathogenesis of PKS is mainly due to the global abnormalities of transcription and early embryonic development. The term “melanogenesis” was enriched in downregulated genes. This finding is interesting given that PKS is often associated with hypo and hyperpigmented patches (Figure 1). Extra copies of 12p likely cause dysregulated expression of melanogenesis related genes, leading to the pigmentation abnormalities.
In summary, we demonstrate that PKS probands have a unique gene expression profile, which is likely correlated with the highly specific clinical phenotype. While the expression studies described in the experiment were performed on skin fibroblasts and may not be representative of events occurring in early embryonic tissues, several of the identified misexpressed genes provide insight into individual genes and pathways that would appear to be plausible candidates contributing to several of the PKS clinical features (Figure 6). From previous studies, we expect that a single or a few critical genes on 12p, that when present in extra copy numbers, will have a large scale effect on mammalian cell growth and differentiation likely through a large number (cascade) of intermediary genes. Through these studies we are hoping to both identify critical genes on 12p as well as downstream targets in non-12p chromosomal regions.
Supporting Information
Figure S1.
Scatterplot showing the correlation between 2 technologies (Microarray vs. ddPCR).
https://doi.org/10.1371/journal.pone.0108853.s001
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Table S1.
Genes identified as being up-regulated in patients with PKS.
https://doi.org/10.1371/journal.pone.0108853.s002
(XLS)
Table S2.
List of down-regulated genes in patients with PKS.
https://doi.org/10.1371/journal.pone.0108853.s003
(XLS)
Table S5.
List of all Principal Component values.
https://doi.org/10.1371/journal.pone.0108853.s006
(XLSX)
Table S6.
PKS-control difference of 10 differentially expressed genes selected by Microarray data analysis confirmed by ddPCR.
https://doi.org/10.1371/journal.pone.0108853.s007
(XLSX)
Acknowledgments
We are deeply indebted to the PKS families who participated in this study as well as support from the PKS Kids family support group.
Author Contributions
Conceived and designed the experiments: MK KI AW KC NS LC ZZ IK. Performed the experiments: MK KI. Analyzed the data: MK KI ZZ IK LC. Contributed reagents/materials/analysis tools: MK KI ZZ IK. Wrote the paper: MK KI ZZ IK.
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