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SRX5858971: GSM3778179: RNA_BW35773-T; Peromyscus maniculatus; RNA-Seq
1 ILLUMINA (Illumina HiSeq 4000) run: 68.3M spots, 20.6G bases, 7.8Gb downloads

Submitted by: NCBI (GEO)
Study: Whole Transcriptome RNA-seq in Peromyscus maniculatus fibroblasts
show Abstracthide Abstract
Analysis of gene expression can be challenging, especially if it involves genetically diverse populations that exhibit high variation in their individual expression profile. Despite this variation though, it is conceivable that in the same individuals a high degree of coordination is maintained between transcripts that belong to the same signaling modules and are associated with related biological functions. To explore this further, we calculated the correlation in the expression levels between each of ATF4, CHOP (DDIT3), GRP94, DNAJB9 (ERdj4), DNAJ3C (p58IPK) and HSPA5 (BiP/GRP78) with the whole transcriptome in primary fibroblasts from deer mice following induction of endoplasmic reticulum (ER) stress. Since these genes are associated with different transducers of the unfolded protein response (UPR) we postulated that their profile, in terms of correlation of transcripts, reflects distinct UPR branches engaged and therefore different biological processes. Standard gene ontology analysis was able to predict major functions associated with the corresponding transcript, and of the UPR arm related to that, namely regulation of the apoptotic response by ATF4 (PERK arm) and the ER stress associated degradation for GRP94 (IRE1). BiP, being a global regulator of the UPR, was associated with activation of ER stress in a rather global manner. Pairwise comparison in the correlation coefficients for these genes' associated transcriptome showed the relevance of selected genes in terms of expression profiles. Overall design: Whole Transcriptome expression examination of Peromyscus transcriptome after induction of unfolded protein response
Sample: RNA_BW35773-T
SAMN11672443 • SRS4782831 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 4000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: RNAs were extracted with Qiagen RNeasy Plus Mini kit (Qiagen, Valencia, CA, USA). RNA integrity was assessed using the Agilent Bioanalyzer and samples had a quality score >8.0. RNA libraries were prepared using established protocol with NEBNExt Ultra II Directional Library Prep Kit for Illumina, (NEB, Lynn, MA). Each library was made with one of the TruSeq barcode index sequences and samples were sequenced across three lanes. The pools were clustered at 6.5 pM on a pair end read flow cell and sequenced for 300 cycles on an Illumina Hiseq 4000.
Experiment attributes:
GEO Accession: GSM3778179
Links:
Runs: 1 run, 68.3M spots, 20.6G bases, 7.8Gb
Run# of Spots# of BasesSizePublished
SRR908376068,273,50720.6G7.8Gb2019-05-20

ID:
7869677

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