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SRX8123234: GSM4478568: Anomo_leaf; Anomochloa marantoidea; ncRNA-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 34M spots, 1.7G bases, 1.2Gb downloads

Submitted by: NCBI (GEO)
Study: Small RNAs in monocots
show Abstracthide Abstract
In monocots other than the cereals maize and rice, the repertoire and diversity of microRNAs (miRNAs) and the populations of phased, secondary, small interfering RNAs (phasiRNAs) are poorly characterized. To remedy this, we sequenced small RNAs (sRNAs) from vegetative and dissected inflorescence tissue in 28 phylogenetically diverse monocots and from several early-diverging angiosperm lineages, as well as publicly available data from 10 additional monocot species. We annotated miRNAs, siRNAs and phasiRNAs across the monocot phylogeny, identifying miRNAs apparently lost or gained in the grasses relative to other monocot families, as well as a number of tRNA fragments misannotated as miRNAs. Using our miRNA database cleaned of these misannotations, we identified conservation at the 8th, 9th, 19th and 3' end positions that we hypothesize are signatures of selection for processing, targeting, or Argonaute sorting. We show that 21-nt reproductive phasiRNAs are far more numerous in grass genomes than other monocots. Based on sequenced monocot genomes and transcriptomes, DICER-LIKE 5 (DCL5), important to 24-nt phasiRNA biogenesis, likely originated via gene duplication before the diversification of the grasses. This curated database of phylogenetically diverse monocot miRNAs, siRNAs, and phasiRNAs is the largest collection to date, and should facilitate continued exploration of small RNA diversification in flowering plants. Overall design: Small RNA (sRNA) sequencing for 28 phylogenetically diverse monocots
Sample: Anomo_leaf
SAMN14605254 • SRS6487670 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2500
Strategy: ncRNA-Seq
Source: TRANSCRIPTOMIC
Selection: size fractionation
Layout: SINGLE
Construction protocol: sRNA library constructed from all diverse tissue types listed in the field "source name" . The small RNA libraries were generated as described by Lu et al. (Methods 2007, 43:110), followed by Illumina sRNA TruSeq sample preparation kit followed by sequencing with Illumina's HiSeq 2500 instrument. The adapter sequences were removed, and the abundance of each distinct small RNA was determined.
Experiment attributes:
GEO Accession: GSM4478568
Links:
Runs: 1 run, 34M spots, 1.7G bases, 1.2Gb
Run# of Spots# of BasesSizePublished
SRR1155360634,001,9871.7G1.2Gb2020-04-17

ID:
10573156

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