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A genome-wide search for epigenetically [corrected] regulated genes in zebra finch using MethylCap-seq and RNA-seq.
- Source :
-
Scientific reports [Sci Rep] 2016 Feb 11; Vol. 6, pp. 20957. Date of Electronic Publication: 2016 Feb 11. - Publication Year :
- 2016
-
Abstract
- Learning and memory formation are known to require dynamic CpG (de)methylation and gene expression changes. Here, we aimed at establishing a genome-wide DNA methylation map of the zebra finch genome, a model organism in neuroscience, as well as identifying putatively epigenetically regulated genes. RNA- and MethylCap-seq experiments were performed on two zebra finch cell lines in presence or absence of 5-aza-2'-deoxycytidine induced demethylation. First, the MethylCap-seq methodology was validated in zebra finch by comparison with RRBS-generated data. To assess the influence of (variable) methylation on gene expression, RNA-seq experiments were performed as well. Comparison of RNA-seq and MethylCap-seq results showed that at least 357 of the 3,457 AZA-upregulated genes are putatively regulated by methylation in the promoter region, for which a pathway analysis showed remarkable enrichment for neurological networks. A subset of genes was validated using Exon Arrays, quantitative RT-PCR and CpG pyrosequencing on bisulfite-treated samples. To our knowledge, this study provides the first genome-wide DNA methylation map of the zebra finch genome as well as a comprehensive set of genes of which transcription is under putative methylation control.
- Subjects :
- Animals
Avian Proteins metabolism
Azacitidine analogs & derivatives
Azacitidine pharmacology
Cell Line, Tumor
CpG Islands
DNA Methylation drug effects
Decitabine
Female
Finches metabolism
Gene Regulatory Networks
Learning physiology
Male
Memory physiology
Nerve Tissue Proteins metabolism
Promoter Regions, Genetic
Sequence Analysis, DNA
Sequence Analysis, RNA
Avian Proteins genetics
Epigenesis, Genetic
Finches genetics
Genome
Nerve Tissue Proteins genetics
Subjects
Details
- Language :
- English
- ISSN :
- 2045-2322
- Volume :
- 6
- Database :
- MEDLINE
- Journal :
- Scientific reports
- Publication Type :
- Academic Journal
- Accession number :
- 26864856
- Full Text :
- https://doi.org/10.1038/srep20957