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SRX849202: GSM1587999: YH-A-2; Raphanus sativus; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 12M spots, 3.6G bases, 2.2Gb downloads

Submitted by: Gene Expression Omnibus (GEO)
Study: Identification of differentially expressed genes related to cytoplasmic male sterility in radish (Raphanus sativus L.) by comparative transcriptome analysis
show Abstracthide Abstract
Cytoplasmic male sterility (CMS), a typically maternally inherited trait, causes a failure in producing functional pollen. Although the radish CMS has be widely used to produce hybrid varieties in breeding program, the molecular mechanism of CMS in radish is poorly understood. In this study, two radish CMS lines (HYBP-A and YH-A) and their corresponding maintainer lines (HYBP-B and YH-B) were used to identify genes potentially involving in CMS using Illumina pair-end sequencing. A total of 167.86 million clean sequence reads were generated from the eight libraries (two replicates for each line). These reads were eventually assembled into 130,240 unigenes. Of them, 67,173 (51.6%) unigenes were annotated for their function. Comparison of gene expression levels between CMS line and maintainer line revealed 5,893 differentially expressed genes (DEGs) in HYBP, and 3,739 DEGs inYH. There were 990 DEGs commonly identified in both HYBP and YH, with same direction of expression change in two CMS lines relative to their corresponding maintainer lines, which suggested these 990 DEGs is likely related to CMS of radish. The expression levels of 20 DEGs were further confirmed by real-time quantitative PCR (qRT-PCR). Two pathways and eight functional categories exhibited a significant enrichment with DEGs in HYBP, and one pathway and six functional categories were markedly enriched by DEGs in YH. Among these pathways/functional categories, four of them were enriched in both varieties. A series of candidate genes and pathways that may contribute to the CMS will be helpful for increasing our understanding for this trait in radish. Overall design: Two CMS lines and two their corresponding maintainer lines were used. a total of eight samples, i.e. two replicates for each line were used for RNA-seq.
Sample: YH-A-2
SAMN03289350 • SRS824135 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: The dual-core period anthers of microspore mother cells of two CMS lines and two maintainer lines were corrected. Anthers collected from five individuals for each line were mixed as a sample. Total RNA of each sample was extracted using an E.Z.N.A. Plant RNA Kit (OMEGA Bio-Tek, USA) according to the manufacturer’s protocol. RNA of four samples were separately used to construct the cDNA library with a fragment length ranging from 200 to 500 bp. Then, the paired-end sequencing was performed by using the Illumina sequencing platform (HiSeqTM 2500) according to the manufacturer’s instructions (Illumina, San Diego, CA).
Experiment attributes:
GEO Accession: GSM1587999
Links:
External link:
Runs: 1 run, 12M spots, 3.6G bases, 2.2Gb
Run# of Spots# of BasesSizePublished
SRR176793112,000,0003.6G2.2Gb2016-01-21

ID:
1199055

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