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SRX24242276: GSM8207445: wild type, 20C, rep 3; Caenorhabditis elegans; ncRNA-Seq
1 ILLUMINA (HiSeq X Ten) run: 30.1M spots, 4.5G bases, 1.8Gb downloads

External Id: GSM8207445_r1
Submitted by: Department of Biology, Colorado State University
Study: Regulation of Microprocessor assembly and localization via Pasha's WW domain in C. elegans
show Abstracthide Abstract
Primary microRNA (pri-miRNA) transcripts are processed by a protein complex called the Microprocessor comprised of the ribonuclease Drosha and its RNA binding partner DGCR8/Pasha. We sequenced small RNAs from animals containing a mutation in the WW domain of C. elegans pash-1. We found that these mutants have a modest but widespread reduction in miRNA levels when grown at 20°C, which is further enhanced when grown at 25°C. The results demonstrate a requirement for the WW domain in processing miRNAs in C. elegans. Overall design: Small RNA high-throughput sequencing was done using RNA isolated from wild type and pash-1(ram33)mutant whole gravid adult C. elegans grown at 20°C or 25°C. The tinyRNA pipeline was used to quantitatively assess miRNA levels.
Sample: wild type, 20C, rep 3
SAMN40951218 • SRS21010463 • All experiments • All runs
Library:
Name: GSM8207445
Instrument: HiSeq X Ten
Strategy: ncRNA-Seq
Source: TRANSCRIPTOMIC
Selection: size fractionation
Layout: SINGLE
Construction protocol: Worms were washed from plates and rinsed with M9 3 times and flash frozed in liquid nitrogen. RNA was isolated using trizol/chloroform and isopropanol precipitation. Libraries were then prepared from total RNA according to the NEBNext® Multiplex Small RNA kit protocol. PCR products (~134-148 bp) were size selected using 10% polyacrylamide gels. small RNA-seq
Runs: 1 run, 30.1M spots, 4.5G bases, 1.8Gb
Run# of Spots# of BasesSizePublished
SRR2867396030,087,0894.5G1.8Gb2024-04-16

ID:
32554728

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