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SRX1690356: GSM2113610: RNASeq_riboM_lin-41(xe11)_22hr; Caenorhabditis elegans; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 30.9M spots, 1.5G bases, 707.8Mb downloads

Submitted by: NCBI (GEO)
Study: Post-transcriptional regulation by the let-7 microRNA and the TRIM-NHL protein LIN41 [RNA-seq]
show Abstracthide Abstract
We perform RNA sequencing and ribosome profiling time course experiments to examine the effect of fully dysregulating all let-7 targets (in let-7(n2853) animals), partially dysregulating only LIN41 (in lin-41(xe11) animals) or fully dysregulating all let-7 targets while partially dysregulating LIN41 in lin-41(xe11); let-7(n2853) double mutant animals. We conclude that effects on gene expression in let-7 mutant animals are largely and quantitatively explained by dysregulation of LIN41 as its primary target. Furthermore, we identify direct LIN41 target genes regulated on the level of translation or mRNA abundance. Overall design: Total RNA-sequencing time course experiments sampling synchronized worm populations of different genetic backgrounds every two hours over the course of development from late L2/early L3 stage to late L4/Young adult stage.
Sample: RNASeq_riboM_lin-41(xe11)_22hr
SAMN04633134 • SRS1393970 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Total RNA isolation was performed using Tri-Reagent (MRC). To obtain ribosomal RNA (rRNA)-depleted total RNA, a DNase-treatment was performed with the RNase-Free DNase Set (Qiagen) and the RNeasy MiniKit (Qiagen), before using the Ribo-Zero rRNA Removal Kit (Epicentre) to remove rRNA. Library preparation was performed using the ScriptSeq v2 RNA-Seq library preparation kit (Epicentre) according to the manufacturer's protocol
Experiment attributes:
GEO Accession: GSM2113610
Links:
Runs: 1 run, 30.9M spots, 1.5G bases, 707.8Mb
Run# of Spots# of BasesSizePublished
SRR335663630,852,5691.5G707.8Mb2017-07-18

ID:
2425132

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