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SRX14620028: hrde1_F1_controlRNAi_rep_2_TTAGGC_sRNAseq
1 ILLUMINA (Illumina HiSeq 2500) run: 27.3M spots, 1.3G bases, 767.6Mb downloads

Design: RNA extraction was performed on up to 100 uL of worms flash frozen in liquid nitrogen and stored at -80 C. Frozen samples were resuspended in 1 mL of Trizol (ThermoFisher; Cat #: 15596026), subjected to three freeze-thaw cycles, and incubated at room temperature for five minutes with shaking at 1500 RPM in a benchtop shaker (Benchmark Scientific; Model #: H5000-HC) and an additional five minutes without shaking. 200 uL of chloroform was added to each tube, and the samples were shaken by hand for 15 seconds, followed by a 2-3 minute incubation at room temperature, and 12,000xg spin at 4 C for 15 minutes. The upper aqueous phase was removed and an equal volume of 95-100% ethanol was added and mixed. Samples were concentrated and purified using the Zymo RNA Clean & Concentrator Kit columns (Zymo; Cat #: R1017). On-column DNase I digestions with MgCl2 buffer (ThermoFisher; Cat # EN0521) were used for each RNA prep to remove contaminating DNA. Samples were eluted in water. Small RNA libraries were prepared as follows: 5 ug of extracted total RNA was treated with 5 polyphosphatase (20 U/ug of RNA) for 30 minutes at 37 C and purified using the Zymo RNA Clean & Concentrator Kit columns (Zymo; Cat #: R1017). 1 ug of treated RNA was inputted into the Illumina TruSeq Small RNA Library Preparation Kit (Illumina; Cat #: RS-200-0012) with 11 cycles of PCR amplification. Libraries were run on either a 6% Novex TBE gel or a 5% Criterion TBE gel and size selected according to the Illumina protocol. Purified samples were sequenced on the Illumina HiSeq2500 at the Johns Hopkins University School of Medicine Genetic Resources Core Facility. mRNAseq libraries were generated using 1 ug of total RNA with the TruSeq Stranded Total RNA Library Prep Gold (Illumina; Cat # 20020598). 2 uL of a 1:100 dilution of the ERCC RNA Spike-In Mix #1 (ThermoFisher; Cat #: 4456740) was added to the total RNA prior to library preparation. TruSeq RNA UD Indexes were used for indexing (Illumina; Cat #: 20022371), and libraries were pooled for sequencing on the NovaSeq6000 at the Johns Hopkins University School of Medicine Genetic Resources Core Facility.
Submitted by: The Johns Hopkins University School of Medicine
Study: The conserved helicase ZNFX-1 memorializes silenced RNAs in nuage
show Abstracthide Abstract
RNA-mediated interference (RNAi) is a conserved mechanism that uses small RNAs (sRNAs) to silence gene expression. In the C. elegans germline, transcripts targeted by sRNAs are used as templates for sRNA amplification to propagate silencing into the next generation. We find that RNAi leads to heritable changes in the distribution of nascent and mature transcripts that correlate with two parallel sRNA amplification loops. The first loop, dependent on the nuclear Argonaute HRDE-1, targets nascent transcripts and reduces but does not eliminate productive transcription at the locus. The second loop, dependent on the conserved helicase ZNFX-1, targets mature transcripts and concentrates them in perinuclear condensates (nuage). ZNFX-1 interacts with sRNA-targeted transcripts that have acquired poly-UG tails and is required to sustain pUGylation and robust sRNA amplification in the inheriting generation. By maintaining a pool of transcripts for amplification, ZNFX-1 prevents premature extinction of the RNAi response and perpetuates silencing into the next generation.
Sample: hrde1_F1_controlRNAi_rep_2_TTAGGC_sRNAseq
SAMN26935013 • SRS12387549 • All experiments • All runs
Library:
Name: hrde1_F1_controlRNAi_rep_2_TTAGGC_sRNAseq
Instrument: Illumina HiSeq 2500
Strategy: miRNA-Seq
Source: TRANSCRIPTOMIC
Selection: PCR
Layout: SINGLE
Runs: 1 run, 27.3M spots, 1.3G bases, 767.6Mb
Run# of Spots# of BasesSizePublished
SRR1848842827,283,2371.3G767.6Mb2022-04-02

ID:
20899703

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