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SRX984390: GSM1649171: SF1 brain (RNA-seq); Heterocephalus glaber; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 23.1M spots, 4.2G bases, 2.7Gb downloads

Submitted by: Gene Expression Omnibus (GEO)
Study: Hormonal and stress-response pathways regulate naked mole rat eusociality
show Abstracthide Abstract
Naked mole rats live in eusocial colonies where subordinates help a single dominant female and a few males to breed. We investigated the genome-wide regulatory mechanisms underlying their reproductive division of labor by examining brain and gonad transcriptomes and DNA-methylomes. Subtle expression differences were observed between brains of dominants and subordinates, but differentially expressed genes clustered consistently in a module with similar function for both sexes. Gonadotropin-releasing hormone (GNRH1) was central in this module and linked with stress-response genes such as neuropeptide Y and corticotrophin-releasing hormone. Breeder-subordinate modifications in DNA methylation were substantial in male brains and associated with the GNRH1 module. The GNRH1-regulated estrogen synthesis pathway was completely blocked in subordinate ovaries and sperm-related genes were significantly down-regulated in subordinate testes. Our results indicate that reproductive suppression is based on hormonal- and stress-related control by the dominant female, but with significant differences in molecular mechanisms between males and females. Overall design: Naked mole rats were housed in our laboratory. Animals were sacrificed, and the tissues immediately frozen and stored in liquid nitrogen. Tissues were obtained from male (n = 2) and female (n = 2) breeders as well as male (n = 2) and female (n = 2) non-breeders (subordinates). We analyzed brains from all eight individuals separately, but female ovaries were only large enough for individual analysis in breeders, whereas subordinate ovaries were so small that 3–5 of them had to be pooled for gene expression analyses. The testes of breeding and non-breeding males were not visually different, but breeder status was known because these males had previously sired pups.
Sample: SF1 brain (RNA-seq)
SAMN03468210 • SRS899003 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: For RNA-seq library construction, 2 μg total RNA per sample was treated with DNase I (New England BioLabs) to remove possible contamination with genomic DNA. Then poly (A+) mRNA was purified from the total RNA using the Dynabeads mRNA Purification Kit (Invitrogen), followed by fragmentation using the RNA fragmentation kit (Ambion). Next, the first cDNA strand was synthesized using random hexamer primers and reverse transcriptase (Invitrogen), and second-strand cDNA was synthesized using DNA polymerase I (New England BioLabs). After that, the synthetic double-stranded cDNA was end repaired, followed by 3’-end addition of dA, adapter ligation and size selection according to Illumina’s protocols. Finally, the selected products were amplified by 15 PCR cycles to yield the RNA-seq libraries. All RNA-seq libraries were subjected to 90 bp paired-end sequencing on an Illumina HiSeq 2000 platform. We analyzed brains from all eight individuals separately, but female ovaries were only large enough for individual analysis in breeders, whereas subordinate ovaries were so small that 3–5 of them had to be pooled for gene expression analyses. The testes of breeding and non-breeding males were not visually different, but breeder status was known because these males had previously sired pups. RNA and DNA were isolated as described in Kim, et al. Nature (2011).
Experiment attributes:
GEO Accession: GSM1649171
Links:
External link:
Runs: 1 run, 23.1M spots, 4.2G bases, 2.7Gb
Run# of Spots# of BasesSizePublished
SRR195914223,138,1874.2G2.7Gb2017-03-31

ID:
1431914

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