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SRX23452306: GSM8046438: small RNA-seq: RIL003-1.5mm-rep2; Zea luxurians; ncRNA-Seq
1 ILLUMINA (NextSeq 550) run: 46.5M spots, 3.5G bases, 1.3Gb downloads

External Id: GSM8046438_r1
Submitted by: Huazhong Agricultural University
Study: Premeiotic 24-nt phasiRNAs are present in the Zea genus and unique in biogenesis mechanism and molecular function [small_RNA]
show Abstracthide Abstract
Reproductive phasiRNAs are broadly present in angiosperms and play crucial roles in sustaining male fertility. While the premeiotic 21-nt phasiRNAs and meiotic 24-nt phasiRNA pathways have been extensively studied in maize (Zea mays) and rice (Oryza sativa), a third putative category of reproductive phasiRNAs–named premeiotic 24-nt phasiRNAs–have recently been reported in barley (Hordeum vulgare) and wheat (Triticum aestivum). To determine whether premeiotic 24-nt phasiRNAs are also present in maize and related species and begin to characterize their biogenesis and function, we performed a comparative transcriptome and degradome analysis of premeiotic and meiotic anthers from five maize inbred lines and three teosinte species/subspecies. Our data indicate that a substantial subset of the 24-nt phasiRNA loci in maize and teosinte are already highly expressed at premeiotic phase. The premeiotic 24-nt phasiRNAs are similar to meiotic 24-nt phasiRNAs in genomic origin and dependence on DCL5 for biogenesis, but premeiotic 24-nt phasiRNAs are unique in that they are likely (i) not triggered by microRNAs, (ii) not loaded by AGO18 proteins, and (iii) not capable of mediating cis-cleavage. In addition, we also observed a group of premeiotic 24-nt phasiRNAs in rice using previously published data. Together, our results indicate that the premeiotic 24-nt phasiRNAs constitute a unique class of reproductive phasiRNAs and are present more broadly in the grass lineage than previously known. Overall design: Small RNA and degradome profiling of anther materials from five maize inbred lines, a maize mutant, and three teosinte species or subspecies Please note that the *mm in sample titles represents the length of the anther used for the corresponding sample (e.g. 0.4-mm anther for 'B73-0.4mm-rep1' sample), and that the 'ago18HM' and 'ago18HT' represents 'ago18 triple homozygous mutant' and 'ago18 triple heterozygote', respectively.
Sample: small RNA-seq: RIL003-1.5mm-rep2
SAMN39674268 • SRS20305350 • All experiments • All runs
Organism: Zea luxurians
Library:
Name: GSM8046438
Instrument: NextSeq 550
Strategy: ncRNA-Seq
Source: TRANSCRIPTOMIC
Selection: size fractionation
Layout: SINGLE
Construction protocol: Fresh anthers were snap-frozen in liquid nitrogen and total RNA was extracted using the TRI reagent (Sigma-Aldrich) or the TraPR Small RNA Isolation kit (Lexogen; for TraPR sRNA-seq only) sRNA-seq libraries were prepared from ~100 ng total RNA per sample using a Somagenics RealSeq-AC miRNA library kit following the manufacturer's protocol. RNA-seq (Smart-seq2) and nanoPARE libraries were prepared from 5 ng total RNA per sample using the nanoPARE library preparation protocol.
Runs: 1 run, 46.5M spots, 3.5G bases, 1.3Gb
Run# of Spots# of BasesSizePublished
SRR2778755046,492,8293.5G1.3Gb2024-05-14

ID:
31683513

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