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DRX479939: ZT12_Ribo-seq_rep1
1 ILLUMINA (Illumina HiSeq 2500) run: 65.9M spots, 3.3G bases, 2.5Gb downloads

Submitted by: UT_IBIO
Study: Impact of translational regulation on diel expression revealed by time-series ribosome profiling in Arabidopsis
show Abstracthide Abstract
Plants have developed the ability to adjust to the day/night cycle through the expression of diel genes, which allow them to effectively respond to environmental changes and optimise their growth and development. Diel oscillations also have substantial implications in many physiological processes, including photosynthesis, floral development, and environmental stress responses. The expression of diel genes is regulated by a combination of the circadian clock and responses to environmental cues, such as light and temperature. A great deal of information is available on the transcriptional regulation of diel gene expression. However, the extent to which translational regulation is involved in controlling diel changes in expression is not yet clear. To investigate the impact of translational regulation on diel expression, we conducted Ribo-seq and RNA-seq analyses on a time-series sample of Arabidopsis shoots cultivated under a 12?h light/dark cycle. Our results showed that translational regulation is involved in about 71% of the genes exhibiting diel changes in mRNA abundance or translational activity, including clock genes, many of which are subject to both translational and transcriptional control. They also revealed that the diel expression of glycosylation and ion-transporter-related genes is mainly established through translational regulation. The expression of several diel genes likely subject to translational regulation through upstream open-reading frames was also determined.
Sample: zt12_1
SAMD00621648 • DRS369154 • All experiments • All runs
Library:
Name: zt12_1_ribo
Instrument: Illumina HiSeq 2500
Strategy: OTHER
Source: TRANSCRIPTOMIC
Selection: other
Layout: SINGLE
Construction protocol: Library preparation for Ribo-seq and RNA-seq was performed for two biological replicates for each time point. Approximately 1.5 g of frozen tissue powder of the Arabidopsis whole shoot was used for single Ribo-seq library construction. Ribosome footprint extraction and the subsequent library construction were performed as described previously (Sotta et al. 2022). Final amplification of the libraries was conducted by 9 cycles of PCR. For RNA-seq library preparation, total RNA was extracted from approximately 50 mg of frozen tissue powder of the whole shoot using a RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). DNA and rRNA were depleted by a Turbo DNA-free Kit (Thermo Fisher Scientific, Waltham, MA, USA) and a Ribo-Zero Plant Leaf kit (Illumina, San Diego, CA, USA), respectively. Enriched mRNA was used for library construction using TruSeq Stranded Total RNA Library Prep Plant kit (Illumina, San Diego, CA, USA).
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1NIL
Runs: 1 run, 65.9M spots, 3.3G bases, 2.5Gb
Run# of Spots# of BasesSizePublished
DRR49576865,894,0053.3G2.5Gb2024-03-21

ID:
32320659

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