U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

SRX469417: GSM1325466: IPO323_YMS; Zymoseptoria tritici; RNA-Seq
3 ILLUMINA (Illumina HiSeq 2000) runs: 217.7M spots, 10.9G bases, 7.3Gb downloads

Submitted by: Gene Expression Omnibus (GEO)
Study: Transcriptome sequencing at early stage infection of the wheat pathogen Zymoseptoria tritici reveals chromosomal differences in transcription patterns and host specific gene expression.
show Abstracthide Abstract
We have applied whole transcriptome profiling to infer genetic determinants of pathogenicity and host specialization in Z. tritici. Our data includes RNAseq data from early infection stages of a compatible (wheat) and a non-compatible host (Brachypodium distachyon). Overall transcription of AC genes is remarkably lower than genes on core chromosomes (CC) and only 40% of the genes are transcribed. We identify 31 AC and 1069 CC genes showing plant specific expression. In addition 21 CC genes are only upregulated in wheat supporting functional relevance in host specificity. We further explore the genomic composition and distribution of unique and paralogous genes in Z. tritici focusing on the evolutionary origin of AC genes. In contrast to previous studies we show that ACs mainly encode unique genes. Phylogenetic analyses suggest that rare duplication events in the Z. tritici genome precede diversification of Zymoseptoria species and demonstrate that ACs have been maintained in the genome of Zymoseptoria over long evolutionary times. Overall design: Examination of gene expression at 3 different growth condition of the wheat pathogen Z. tritici.
Sample: IPO323_YMS
SAMN02640204 • SRS556705 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: To extract total RNA from fungal axenic culture or freeze-dried leaf tissue infected with Z. tritici, 100 mg of sample was crushed in liquid nitrogen and total RNA was extracted using the TRIZOL reagent (Invitrogen) following the manufacturer’s protocol. RNA samples were purified twice with Dynal oligo(dT) magnetic beads (Invitrogen), following the manufacturer's instructions. RNA-seq libraries for plant infection replicates were prepared from an input of 4 µg total purified polyA RNA according to recommendations of the supplier (TruSeq RNA sample preparation v2 guide, Illumina).
Experiment attributes:
GEO Accession: GSM1325466
Links:
External link:
Runs: 3 runs, 217.7M spots, 10.9G bases, 7.3Gb
Run# of Spots# of BasesSizePublished
SRR116771674,954,8153.7G2.5Gb2014-07-01
SRR116771770,355,8513.5G2.4Gb2014-07-01
SRR116771872,422,2293.6G2.4Gb2014-07-01

ID:
649605

Supplemental Content

Search details

See more...

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...