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SRX3854634: GSM3069681: Pvir#6_hep [RNA-seq]; Procambarus virginalis; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 52.8M spots, 10.7G bases, 6.7Gb downloads

Submitted by: NCBI (GEO)
Study: Genome-wide mapping and functional analysis of DNA methylation in clonal invasive crayfish [RNA-seq]
show Abstracthide Abstract
The marbled crayfish (Procambarus virginalis) is a unique freshwater crayfish characterized by genetic uniformity, phenotypic variability, and substantial invasive potential. As invasion into different habitats occurs in the absence of genetic variation, epigenetic mechanisms have been suggested to mediate phenotypic adaptation. However, epigenetic regulation has not been analyzed in this organism yet. Here we show that the recently published P. virginalis draft genome sequence encodes a conserved DNA methylation system. Whole-genome bisulfite sequencing of multiple replicates and different tissues revealed a methylation pattern that is characterized by gene body methylation of housekeeping genes. Interestingly, this pattern was largely tissue-invariant, suggesting a function that is unrelated to cell-fate specification. Indeed, integrative analysis of RNA-seq datasets showed that gene body methylation correlated with stable gene expression, while unmethylated genes often showed a high degree of inter-individual expression variation. Our findings thus establish the methylome of an emerging model organism and suggest that methylation-dependent regulation of gene expression variability may facilitate the phenotypic adaptation and invasive spread of this animal. Overall design: RNA-seq data of different tissues (hepatopancreas, abdominal musculature) from 6 different P. virginalis individuals and 2 different P. fallax individuals
Sample: Pvir#6_hep [RNA-seq]
SAMN08802952 • SRS3098601 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Total RNA was isolated from 20-60 mg frozen tissues. Thawed tissues were homogenized in 1 ml Trizol (Ambion), precipitated with isopropanol and resuspended in 20-100 µl RNase-free water (Gibco Life Technologies). Total RNA was treated with DNase using the RNeasy Mini Kit (Qiagen) following the manufacturer's RNeasy Mini Protocol for RNA Cleanup in combination with the On-Column DNase Digestion Protocol. Sequencing libraries were prepared using 1µg of DNAse-treated total RNA in the first step of the TruSeq RNA Sample Preparation v2 protocol (Illumina, Part# 15026495 Rev. A) as recommended by the manufacturer.
Experiment attributes:
GEO Accession: GSM3069681
Links:
Runs: 1 run, 52.8M spots, 10.7G bases, 6.7Gb
Run# of Spots# of BasesSizePublished
SRR690602652,755,05210.7G6.7Gb2018-10-11

ID:
5300650

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