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SRX641359: GSM1422374: mont_acc_1; Drosophila montana; RNA-Seq
1 ABI_SOLID (AB 5500xl Genetic Analyzer) run: 6.7M spots, 741.9M bases, 419Mb downloads

Submitted by: Gene Expression Omnibus (GEO)
Study: Transcriptome changes associated with cold acclimation in two species of the Drosophila virilis group
show Abstracthide Abstract
For many organisms the ability to cold acclimate with the onset of seasonal cold has major implications for their fitness. In insects, where this ability is widespread, the physiological changes associated with increased cold tolerance have been well studied. Despite this, little work has been done to trace changes in gene expression during cold acclimation that lead to an increase in cold tolerance. We used an RNA-Seq approach to investigate this in two species of the Drosophila virilis group. We found that the majority of genes that are differentially expressed during cold acclimation differ between the two species. Despite this, the biological processes associated with the differentially expressed genes were broadly similar in the two species. These included: metabolism, cell membrane composition, and circadian rhythms, which are largely consistent with previous work on cold acclimation / cold tolerance. In addition, we also found evidence of the involvement of the rhodopsin pathway in cold acclimation, a pathway that has been recently linked to thermotaxis. Interestingly, we found no evidence of differential expression of stress genes implying that long-term cold acclimation and short-term stress response may have a different physiological basis. Overall design: Whole fly mRNA-seq using the SOLiD 5500 XL and SOLiD V4 of two speices of fly (drosophila montana and drosophila virilis) cold acclimated or kept at ambient temperature
Sample: mont_acc_1
SAMN02898088 • SRS650313 • All experiments • All runs
Library:
Instrument: AB 5500xl Genetic Analyzer
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Frozen flies were pooled. RNA was extracted from each sample using Tri Reagent (Sigma-Aldrich) followed by RNeasy Mini kit (Qiagen) purification with DNase treatment. RNA libraries were prepared for sequencing using standard SOLiD protocols
Experiment attributes:
GEO Accession: GSM1422374
Links:
External link:
Runs: 1 run, 6.7M spots, 741.9M bases, 419Mb
Run# of Spots# of BasesSizePublished
SRR15012626,744,684741.9M419Mb2014-12-29

ID:
897259

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