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SRX14337127: GSM5929310: leaf, Zn_CMV_3; Arabidopsis halleri; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 14.6M spots, 1.1G bases, 504.9Mb downloads

External Id: GSM5929310_r1
Submitted by: Ritsumeikan University
Study: A resilient mutualistic interaction between cucumber mosaic virus and its natural host Arabidopsis halleri to adapt to an environmental change
show Abstracthide Abstract
A pseudometallophyte Arabidopsis halleri is frequently found to be infected with cucumber mosaic virus (CMV) in its natural habitat. The purpose of this study is to elucidate the effect of CMV infection on its natural hosts. The CMV(Ho) strain isolated from A. halleri was inoculated into clonal A. halleri plants that were obtained from runners of mother plants, and the pathosystem consisting of CMV(Ho) and its natural host A. halleri was established.In low heavy metal environment, the CMV(Ho) infection caused growth retardation in the above-ground part (stems and leaves) of host plants, and thereby conferred strong drought tolerance on host plants. On the other hand, in high heavy metal environment, which simulates a natural habitat for A halleri, the CMV(Ho) infection did not cause any symptoms to host plants and conferred mild drought tolerance. And the result of transcriptome analysis suggests that CMV(Ho) is recognized as a symbiont rather than a pathogen by its host plant. These results indicate a resilient mutualistic interaction between CMV(Ho) and its natural host A. halleri to adapt to an environmental change. Overall design: RNA-seq is perfomed using three CMV-free, three CMV-infected, three CMV-free zinc excess and three CMV-infected zinc excess leaves of Arabidopsis halleri.
Sample: leaf, Zn_CMV_3
SAMN26363617 • SRS12151359 • All experiments • All runs
Library:
Name: GSM5929310
Instrument: Illumina HiSeq 2500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Total RNAs were extracted by using the Trizol reagent following the manufacturer's protocol (Thermo Fisher Scientific, MA). Library preparation was performed using a TruSeq stranded mRNA sample prep kit (Illumina, San Diego, CA) according to the manufacturer's instructions.
Runs: 1 run, 14.6M spots, 1.1G bases, 504.9Mb
Run# of Spots# of BasesSizePublished
SRR1819048414,633,0001.1G504.9Mb2022-03-05

ID:
20335591

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