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SRX7651957: GSM4290681: DP61 dCLCrV:GhSFT rep2; Gossypium hirsutum; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 38.1M spots, 1.9G bases, 1.2Gb downloads

Submitted by: NCBI (GEO)
Study: SINGLE FLOWER TRUSS and SELF-PRUNING differentially regulate developmental and metabolic genetic networks to guide cotton (Gossypium hirsutum) architectures [GEO_SFT_SP]
show Abstracthide Abstract
Patterns of indeterminate and determinate growth specify plant architecture and influence crop productivity. In cotton (Gossypium hirsutum), SINGLE FLOWER TRUSS (SFT) stimulates the transition to flowering and determinate growth while its closely related antagonist SELF-PRUNING (SP) maintains meristems in indeterminate states to favor vegetative growth. To identify the molecular programs regulating cotton growth habits, and understand how altered expression of GhSFT and GhSP perturbs these programs, we used RNA-Seq to determine the gene expression networks involved in wild photoperiodic, domesticated day-neutral, and GhSFT- and GhSP-regulated architectures. GhSFT or GhSP affected the expression of genes regulating meristem fate and metabolic pathways. Gene ontology analysis predicted enrichment of transcripts involved in photosynthesis, secondary metabolism, and cell wall biosynthesis, and these hypotheses were functionally verified. Weighted gene co-expression network analyses using multiple cotton datasets identified diverse genetic modules highly correlated with SFT or SP, including those that may benefit crop management. Overall design: We used virus-mediated transient gene manipulation to over-express GhSFT from a disarmed Cotton leaf crumple virus (dCLCrV) or silence GhSP from Tobacco rattle virus (TRV) in wild photoperiodic Texas 701 (TX701) and domesticated day-neutral Delta Pine 61 (DP61) cotton varieties.
Sample: DP61 dCLCrV:GhSFT rep2
SAMN13945892 • SRS6081418 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: At 15 days post-inoculation, apices were excised from inoculated seedlings and uninoculated controls, fixed in acetone with vacuum-infiltration, and acetone changed twice before storing at 4°C. Acetone-dried apices were trimmed to 5 mm and expanding leaves were removed. Dried samples were frozen in liquid nitrogen, homogenized using a Retsch mill (Retsch GmbH, Haan, Germany), and RNA isolated by hot borate (Wan and Wilkins, 1994) followed by column clean-up (Zymo Research, Irvine, CA, USA). 2 µg of total RNA from uninoculated, dCLCrV:GhSFT-, and TRV:GhSP-infected DP61 and TX701 plants were used to prepare Illumina TruSeq Stranded mRNA libraries (Illumina, Inc., San Diego, CA, USA) as per the manufacturer's protocols, with three biological replicates per treatment per accession. Libraries were sequenced on a HiSeq2000 (the University of Texas Southwestern Genomics Core), and >30 million 50 bp single-end reads were obtained per replicate.
Experiment attributes:
GEO Accession: GSM4290681
Links:
Runs: 1 run, 38.1M spots, 1.9G bases, 1.2Gb
Run# of Spots# of BasesSizePublished
SRR1099055138,116,3031.9G1.2Gb2020-06-30

ID:
9983046

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