Gene Expression Nebulas
A data portal of transcriptomic profiles analyzed by a unified pipeline across multiple species

Gene Expression Nebulas

A data portal of transcriptome profiles across multiple species

PRJDB2204: Rice germline‐specific Argonaute MEL 1 protein binds to phasiRNA s generated from more than 700 lincRNA s

Source: DDBJ / DRP001762
Submission Date: -
Release Date: Apr 07 2014
Update Date: -

Summary: Small RNA s that interact with Argonaute (AGO ) proteins play central roles in RNA‐mediated silencing. MEIOSIS ARRESTED AT LEPTOTENE1 (MEL 1), a rice AGO , has specific functions in the development of pre‐meiotic germ cells and the progression of meiosis. Here, we show that MEL 1, which is located mostly in the cytoplasm of germ cells, associates preferentially with 21‐nucleotide phased small interfering RNA s (phasiRNA s) that bear a 5′‐terminal cytosine. Most phasiRNA s are derived from 1171 intergenic clusters distributed on all rice chromosomes. From these clusters, over 700 large intergenic, non‐coding RNAs (lincRNA s) that contain the consensus sequence complementary to miR2118 are transcribed specifically in inflorescences, and cleaved within the miR2118 site. Cleaved lincRNA s are processed via DICER ‐LIKE 4 (DCL 4) protein, resulting in production of phasiRNAs. This study provides the evidence that the miR2118‐dependent and the DCL 4‐dependent pathways are both required for biogenesis of 21‐nt phasiRNA s associated with germline‐specific MEL 1 AGO in rice, and over 700 lincRNA s are key factors for induction of this biogenesis during reproductive‐specific stages.

Overall Design: RNA-seq of wild type Nipponbare's anthers

GEN Datasets:
GEND000291
Strategy:
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Protocol
Growth Protocol: All plants were grown in a field in the city of Mishima, Shizuoka, Japan.
Treatment Protocol: The rice (Oryza sativa L., subspecies japonica ) cultivar Nipponbare, was used as the wild type plant. mel1‐1 homozygous mutants were obtained by insertion of an endogenous retrotransposon Tos17, and subsequent backcrosses (three times) with Nipponbare (BC3F4).
Extract Protocol: Total RNA was extracted from pre‐meiotic 0.4‐mm anthers (for RNA‐sequencing and qRT‐PCR) with TRIZOL® Reagent (Life Technologies.
Library Construction Protocol: A total RNA sample was extracted from 0.4‐mm anthers from WT flowers. RNAs (2 μg) purified using oligo(dT) beads were deep sequenced using a Hiseq2000 (Illumina) in accordance with the manufacturer's instructions.
Sequencing
Molecule Type: poly(A)+ RNA
Library Source:
Library Layout: SINGLE
Library Strand: -
Platform: ILLUMINA
Instrument Model: Illumina HiSeq 2000
Strand-Specific: Unspecific
Samples
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Analysis:
Data Resource GEN Sample ID GEN Dataset ID Project ID BioProject ID Sample ID Sample Name BioSample ID Sample Accession Experiment Accession Release Date Submission Date Update Date Species Race Ethnicity Age Age Unit Gender Source Name Tissue Cell Type Cell Subtype Cell Line Disease Disease State Development Stage Mutation Phenotype Case Detail Control Detail Growth Protocol Treatment Protocol Extract Protocol Library Construction Protocol Molecule Type Library Layout Strand-Specific Library Strand Spike-In Strategy Platform Instrument Model Cell Number Reads Number Gbases AvgSpotLen1 AvgSpotLen2 Uniq Mapping Rate Multiple Mapping Rate Coverage Rate
Publications
Rice germline-specific Argonaute MEL1 protein binds to phasiRNAs generated from more than 700 lincRNAs.
The Plant journal : for cell and molecular biology . 2014-04-15 [PMID: 24635777]