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SRX21665185: GSM7766779: P037; Arabidopsis thaliana; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 30.4M spots, 9.1G bases, 2.7Gb downloads

External Id: GSM7766779_r1
Submitted by: Ezer lab, Department of Biology, University of York
Study: Single-plant-omics reveals the cascade of transcriptional changes during the vegetative-to-reproductive transition
show Abstracthide Abstract
A population of wild type plants can contain individuals with drastically different flowering times, due to developmental asynchrony. We performed RNA-seq on individual plants from a large population of wild type (Ws-2) Arabidopsis thaliana, sampling a large number (~70) of replicates at one timepoint during the flowering transition. We have characterised a major transcriptomic switch between plants before and after bolting. Applying methods used in single-cell RNA-seq, we used this data to order the plants by their predicted age – which is referred to as a pseudo-time series. In contrast to a traditional RNA-seq time series, this allows us to view changes in gene expression at a fine temporal scale. Importantly, we can infer the order that transcription factors 'switch on' during the vegetative to floral transition. Overall design: A population of wild type plants were grown under controlled conditions and physiological traits were measured. 75 plants were chosen for sequencing, to represent a diversity of bolting statuses. We then performed RNA-seq and quantified the gene expression of each individual set of plant leaves. In addition, we called variants across the population from the RNA-seq data, to assess the impact of genetic variation on physiology and developmental asynchrony.
Sample: P037
SAMN37318776 • SRS18831733 • All experiments • All runs
Library:
Name: GSM7766779
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Total RNA was isolated from these samples using the Qiagen RNeasy Plant Mini Kit (Cat no. 74904). Residual genomic DNA was removed using the Invitrogen Turbo DNA-free kit (Cat no. AM1907), according to the manufacturer's protocol. Libraries were prepared with the NEBNext Ultra II Directional Library Prep Kit for Illumina (Cat no. E7765), using the NEBNext poly(A) magnetic isolation module (Cat no. E7490). Quality control was performed with the Agilent 2100 Bioanalyzer instrument (Part no. G2939BA). Finally, a total of 70 libraries were pooled and sequenced, via Novagene, using one lane on an Illumina NovaSeq system.
Runs: 1 run, 30.4M spots, 9.1G bases, 2.7Gb
Run# of Spots# of BasesSizePublished
SRR2594661330,401,7679.1G2.7Gb2023-09-11

ID:
29329209

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