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Series GSE147972 Query DataSets for GSE147972
Status Public on Apr 07, 2021
Title DNA methylation regulates transcription factor specific neurodevelopmental but not sexually dimorphic gene expression dynamics in zebra finch telencephalon [RNA-Seq]
Organism Taeniopygia guttata
Experiment type Expression profiling by high throughput sequencing
Summary Song learning in zebra finches is a prototypical example of a complex learned behavior, yet knowledge on the underlying molecular processes is limited. Therefore, we characterized transcriptomic (RNA sequencing) and epigenomic (RRBS, reduced representation bisulfite sequencing; immunofluorescence) dynamics in matched zebra finch telencephalon samples of both sexes from 1 day post hatching (1 dph) to adulthood, spanning the critical period for song learning (20 dph and 65 dph).
We identified extensive transcriptional neurodevelopmental changes during postnatal telencephalon development. DNA (hydroxy)methylation was very low, yet increased over time, particularly in song control nuclei. Only a small fraction of the massive differential expression in the developing zebra finch telencephalon could be explained by differential CpG and CpH DNA methylation. However, a strong association between DNA methylation and age dependent gene expression was found for various transcription factors (i.a. OTX2, AR and FOS) involved in neurodevelopment. Additionally, genomic regions featured by age dependent differential methylation in differentially expressed genes were significantly enriched for specific transcription factor binding motifs. Incomplete dosage compensation was found to be largely responsible for sexually dimorphic gene expression, with dosage compensation increasing throughout life.
In conclusion, our results indicate that DNA methylation regulates neurodevelopmental gene expression dynamics through steering transcription factor activity, but does not explain sexually dimorphic gene expression patterns in zebra finch telencephalon.
 
Overall design For each sex per time point (1 day post hatch (dph), 20dph, 65dph and adult), 3 independent biological replicates were sequenced, resulting in a total of 24 samples. To increase power, each of these biological replicates consisted of a pool of RNA of 3 telencephalons in equal proportions.
 
Contributor(s) Diddens J, Coussement L, Frankl-Vilches C, Majumdar G, Sandra S, ter Haar S, Jeroen G, De Meester E, De Keulenaar S, Wim van C, Cornil CA, Balthazart J, Van Der Linden A, De Meyer T, Vanden Berghe W
Citation(s) 33816458
Submission date Apr 02, 2020
Last update date Apr 07, 2021
Contact name Jeroen Galle
Organization name Ghent University
Department Dept. Of Mathematical Modelling, Statistics and Bioinformatics
Lab Biobix, Lab of Bioinformatics and Computational Genomics
Street address Coupure Links 653
City Ghent
ZIP/Postal code 9000
Country Belgium
 
Platforms (1)
GPL22780 Illumina NextSeq 500 (Taeniopygia guttata)
Samples (24)
GSM4451151 JD-1
GSM4451152 JD-10
GSM4451153 JD-11
This SubSeries is part of SuperSeries:
GSE147974 DNA methylation regulates transcription factor specific neurodevelopmental but not sexually dimorphic gene expression dynamics in zebra finch telencephalon
Relations
BioProject PRJNA622690
SRA SRP255002

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Supplementary file Size Download File type/resource
GSE147972_RNAseq_GEOsubmission.txt.gz 689.0 Kb (ftp)(http) TXT
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