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Series GSE196629 Query DataSets for GSE196629
Status Public on Mar 31, 2022
Title Changes in DNA Methylation Hallmark Alterations In Chromatin Accessibility And Gene Expression For Eye Lens Differentiation [Bisulfite-seq]
Organism Gallus gallus
Experiment type Methylation profiling by high throughput sequencing
Summary Methylation at cytosines (mCG) is a well-known regulator of gene expression but its requirements for cellular differentiation have yet to be fully elucidated. A well-studied cellular differentiation model system is the eye lens, consisting of a single anterior layer of epithelial cells that migrate laterally and differentiate into a core of fiber cells. Here, we explore the genome-wide relationships between mCG methylation, chromatin accessibility and gene expression during differentiation of eye lens epithelial cells into fiber cells. Whole genome bisulfite sequencing identified 7621 genomic loci exhibiting significant differences in mCG levels between lens epithelial and fiber cells. Changes in mCG levels were inversely correlated with the differentiation state-specific expression of 1285 genes preferentially expressed in either lens fiber or lens epithelial cells (Pearson correlation r = -0.37, p < 1x10-42). mCG levels were inversely correlated with chromatin accessibility determined by Assay for transposase-accessible sequencing (ATAC-seq) (Pearson correlation r = -0.86, p < 1x10-300). Many of the genes exhibiting altered regions of DNA methylation, chromatin accessibility and gene expression levels in fiber cells relative to epithelial cells are associated with lens fiber cell structure, homeostasis and transparency. These include lens crystallins (CRYBA4, CRYBB1, CRYGN, CRYBB2), lens beaded filament proteins (BFSP1, BFSP2), transcription factors (HSF4, SOX2, HIF1A), and Notch signaling pathway members (NOTCH1, NOTCH2, HEY1, HES5). Analysis of regions exhibiting cell-type specific alterations in DNA methylation revealed an overrepresentation of consensus sequences of multiple transcription factors known to play key roles in lens cell differentiation including HIF1A, SOX2, and the MAF family of transcription factors. Collectively, these results link DNA methylation with control of chromatin accessibility and gene expression changes required for eye lens differentiation. The results also point to a role for DNA methylation in the regulation of transcription factors previously identified to be important for lens cell differentiation.
 
Overall design Examination of differentially methylated mCG regions between 3 biological replicates of pooled lens epithelial cells and 3 biological replicates of pooled lens fiber cells obtained from embryonic day 13 chick lenses and correlating with differentially expressed genes.
 
Contributor(s) Disatham J, Brennan L, Jiao X, Ma Z, Hejtmancik JF, Kantorow M
Citation(s) 35246225
Submission date Feb 11, 2022
Last update date Mar 31, 2022
Contact name Marc Kantorow
E-mail(s) mkantoro@health.fau.edu
Phone 5612973806
Organization name Florida Atlantic University
Street address 777 Glades Road
City Boca Raton
State/province FL
ZIP/Postal code 33431
Country USA
 
Platforms (1)
GPL19005 Illumina HiSeq 2500 (Gallus gallus)
Samples (6)
GSM5897057 Bisulfite-seq_Lens epithelial cells_rep1
GSM5897058 Bisulfite-seq_Lens epithelial cells_rep2
GSM5897059 Bisulfite-seq_Lens epithelial cells_rep3
This SubSeries is part of SuperSeries:
GSE196631 Changes in DNA Methylation Hallmark Alterations In Chromatin Accessibility And Gene Expression For Eye Lens Differentiation
Relations
BioProject PRJNA806198

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Supplementary file Size Download File type/resource
GSE196629_mCG_DMRs.txt.gz 368.7 Kb (ftp)(http) TXT
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