U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

SRX6385962: GSM3913306: rdr1 rdr2 rdr6 - replicate B; Arabidopsis thaliana; ncRNA-Seq
1 ILLUMINA (NextSeq 500) run: 3.9M spots, 299.5M bases, 96.9Mb downloads

Submitted by: NCBI (GEO)
Study: Arabidopsis RNA Polymerase IV generates 21-22 nucleotide small RNAs that can participate in RNA-directed DNA methylation and may regulate genes
show Abstracthide Abstract
Canonically, Arabidopsis RNA Polymerase IV (Pol IV) is known to produce heterochromatic small RNAs (typically 23-24 nucleotide in length) that maintain silencing of transposable elements (TEs). In contrast, when TEs are transcriptionally activated and produce Pol II transcripts, these transcripts are degraded into 21-22 nt small RNAs (sRNAs) known to participate in post transcriptional gene silencing. Recently, it was reported that Pol IV can also produce 21-22 nt sRNAs in pollen. We investigated the mechanism of Pol IV dependent 21-22 nt sRNAs and show that this mechanism is not specific to pollen. Additionally, we show that these 21-22 nt sRNAs can participate in RNA-directed DNA methylation, are incorporated into ARGONAUTE 1 (AGO1) and may guide AGO1 to cleave genic mRNAs to regulate their expression. Overall design: Examination of total small RNA accumulation in wild-type Columbia and eight mutants. AGO1 protein was immunoprecipitated and small RNAs incorporated in AGO1 was sequenced in wild-type Columbia and pol IV mutant. Whole genome methylC-seq was performed for two mutants.
Sample: rdr1/rdr2/rdr6 sRNA- replicate B
SAMN12173460 • SRS5045470 • All experiments • All runs
Library:
Instrument: NextSeq 500
Strategy: ncRNA-Seq
Source: TRANSCRIPTOMIC
Selection: size fractionation
Layout: SINGLE
Construction protocol: Inflorescence small RNA was isolated with Trizol reagent (Invitrogen) and concentrated using the mirVana microRNA Isolation Kit (Ambion). For AGO1-IP samples, AGO1 was immunocprecipitated from inflorescence tissue using Agrisera anti-AGO1 primary antibody. RNA was isolated from AGO1-IP or mock-IP samples using TriZol reagent. Size-enriched small RNAs were prepared using the TruSeq Small RNA Library Preparation Kit (Illumina). Multiplexed libraries were sequenced on HiSeq2500 or HiSeq4000
Links:
Runs: 1 run, 3.9M spots, 299.5M bases, 96.9Mb
Run# of Spots# of BasesSizePublished
SRR96235223,941,015299.5M96.9Mb2020-02-24

ID:
8459030

Supplemental Content

Search details

See more...

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...