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SRX13356505: GSM5724895: Acala SJ2 control replicate 2; Gossypium hirsutum; RNA-Seq
1 ILLUMINA (Illumina MiSeq) run: 5.4M spots, 1.5G bases, 823.4Mb downloads

Submitted by: NCBI (GEO)
Study: Cotton (Gossypium hirsutum L.) root transcriptional response to the southern Root-Knot Nematode (RKN) Meloidogyne incognita infestation
show Abstracthide Abstract
As an initial step to explore the cotton (Gossypium hirsutum L.) root transcriptional response to the southern Root-Knot Nematode (RKN) Meloidogyne incognita infestation, conventional heirloom G. hirsutum (Gh) cultivars [susceptible Acala SJ-2 (SJ2), moderately resistant Upland Wild Mexico Jack Jones (WMJJ), and resistant Acala NemX] that have been shown to be useful as an informative genetic model for detecting and introgressing RKN resistance genes into commercial Upland cotton were used to enlighten the molecular mechanisms and gene expression of RKN resistance. Using the next generation sequencing (NGS) Illumina MiSeq and HiSeq, we performed RNA-seq profiling in roots with disease progression of 10 days and collected from 23 days old plants of SJ2, WMJJ, and NemX. With three biological replicates of each treatment from each cultivar, plants were subjected to RKN-infestation and non-infested control developing a total of 18 RNA-seq libraries Overall design: Three cotton genotypes (Acala SJ-2 (RKN-susceptible), Wild Mexico Jack Jones (WMJJ; moderately tolerant to RKN) and Acala NemX (RKN-resistant)) and 2 treatments (Control, RKN-infested) were tested. 3 biological replicates for each treatment and genotype.
Sample: Acala SJ2 control replicate 2
SAMN23797440 • SRS11260935 • All experiments • All runs
Library:
Instrument: Illumina MiSeq
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: The root samples from each genotype were grounded in liquid nitrogen, and total RNA was isolated three biological replicates following the manufacturer's instructions using Spectrum TM Plant Total RNA kit (Sigma-Aldrich, St. Louis, MO, USA). The yield and purity of RNA were analyzed with a ND-1000 Spectrophotometer (Nano Drop Technology, Wilmington, DE, USA). Only RNA samples with 1.8 - 2.2 ratio of absorbance 260/280 nm were used for analysis. For each genotype, 2 mg of RNA from each of the three biological-replicates used for cDNA library preparation. The cDNA libraries were prepared following the TruSeq RNA Sample Preparation v2 low sample (LS) protocol guide (Illumina Inc., San Diego, CA USA) Illumina Platform, MiSeq and HiSeq2500
Experiment attributes:
GEO Accession: GSM5724895
Links:
Runs: 1 run, 5.4M spots, 1.5G bases, 823.4Mb
Run# of Spots# of BasesSizePublished
SRR171730405,365,1761.5G823.4Mb2022-04-02

ID:
18352484

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