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SRX998469: GSM1657858: Medicago / Gigaspora replicate 1; Medicago truncatula; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 6.7M spots, 1.3G bases, 856.7Mb downloads

Submitted by: Gene Expression Omnibus (GEO)
Study: An ancient symbiotic fungal gene network revealed by comparative transcriptomics [Grosea_symbiotic_tissues]
show Abstracthide Abstract
Purpose: We here wanted to describe the gene regulation of Gigaspora rosea in association with phyllogenetically divergent plant hosts, and compare these results with gene regulation occuring in R. irregularis, the model arbuscular mycorrhizal fungus. Methods: mRNA from Medicago truncatula (legume), Brachypodium distachyon (grass) in association with G. rosea, and extra radical mycelium of G.rosea were sequenced by Illumina. Reads were mapped on a in-house de novo transcript assembly with the software CLC workbench. Fungal gene expression in the different host plants was compared to extra radical hyphae as reference. Results: Sets of 1891 and 1566 G. rosea genes were highly overexpressed (fold change >5 ; FDR <0,05 and experimental value difference > 10) , in M. truncatula and B. distachyon respectively compared to ERM, among which 802 of them were up-regulated in both plants. Non common up-regulated genes are mainly found non statistically robust in one condition. Conclusions: Our study represents the first transcriptomic analysis on several hosts for this fungal species. These results showed that the interaction between plants and AMF is highly conserved. Overall design: Extra radical and intra radical hyphae in association with 2 phylogenetically divergent plants were produced and gene expression in the different plants were compared to gene expression in extra radical hyphae.
Sample: Medicago / Gigaspora replicate 1
SAMN03490162 • SRS912623 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Biological samples were crushed with a motar and a pestle in liquid nitrogen and mRNA were extracted using RNeasy plant kit (Qiagen), according to the manufacturer instructions. Samples were sequenced at the Genome and Transriptome platform in Toulouse, France (GeT). mRNA were isolated with polyT beads before processing, libraries were constructed according to the manufacturer's protocol.
Experiment attributes:
GEO Accession: GSM1657858
Links:
External link:
Runs: 1 run, 6.7M spots, 1.3G bases, 856.7Mb
Run# of Spots# of BasesSizePublished
SRR19792586,670,8881.3G856.7Mb2016-03-07

ID:
1451031

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