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SRX8111102: GSM4474405: Las_SL2; Lactuca sativa; RNA-Seq
1 ILLUMINA (Illumina HiSeq 4000) run: 43.8M spots, 12.5G bases, 3.7Gb downloads

Submitted by: NCBI (GEO)
Study: Systematic identification and analysis of light-responsive circular RNA and co-expression networks in lettuce (Lactuca sativa)
show Abstracthide Abstract
Circular RNA (circRNA) is a covalently-closed single-stranded RNA molecule that plays an important role in transcriptional regulation of gene expression in a variety of species. Light intensity is a pivotal environmental factor affecting plant growth and development. However, little is known regarding photoresponsive plant circRNAs. Here, we aimed to investigate the expression and function of circRNAs in lettuce leaves in response to different light intensity treatments. We performed RNA sequencing (RNA-Seq) on leaves of lettuce (Lactuca sativa) to determine circRNA expression profiles and reverse-transcription polymerase chain reaction (PCR) to validate the candidate circRNA molecules. We then combined bioinformatics approach to explore the function of the parental genes of circRNA, including network, Gene Ontology, and Kyoto Encyclopedia of Genes and Genomes pathway analysis. We identified 1650 circRNAs in lettuce, of which 1508 (86.40%) were derived from exons. Using real-time PCR, we characterized 10 validated differentially expressed circRNAs and their parental genes, all of which showed expression patterns consistent with RNA-Seq data. Interestingly, the expression of circRNA was, in some cases, inversely correlated with the expression of the parental gene. Furthermore, analysis of the circRNA–microRNA–mRNA network suggests that circRNAs may be involved in plant hormone signaling and chlorophyll metabolism during photoreactivity. These findings provide an essential reference basis for studying circRNAs' biological mechanisms in light-treated plants. Overall design: Lettuce mRNA profiles of 24-day-old 60±2 µmol·m–2·s–1 (Las_WL group. low light intensity), 175±2 µmol·m–2·s–1 (Las_ML group, medium light intensity) and 340±2 µmol·m–2·s–1 (Las_SL group, high light intensity) were generated by deep sequencing, in triplicate, using Illumina Hiseq 4000.
Sample: Las_SL2
SAMN14592372 • SRS6476176 • All experiments • All runs
Organism: Lactuca sativa
Library:
Instrument: Illumina HiSeq 4000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Total RNA was extracted using Trizol reagent (Invitrogen, CA, USA) following the manufacturer's procedure. The total RNA quantity and purity were analysis of Bioanalyzer 2100 and RNA 6000 Nano LabChip Kit (Agilent, CA, USA) with RIN number >7.0. Approximately 5 ug of total RNA representing a specific adipose type was subjected to isolate Poly (A) mRNA with poly-T oligoattached magnetic beads (Invitrogen). Following purification, the poly(A)- or poly(A)+ RNA fractions is fragmented into small pieces using divalent cations under elevated temperature. Then the cleaved RNA fragments were reverse-transcribed to create the final cDNA library in accordance with the protocol for the mRNA-Seq sample preparation kit (Illumina, San Diego, USA), the average insert size for the paired-end libraries was 300 bp (±50 bp). And then we performed the paired-end sequencing on an Illumina Hiseq4000 at the (lc-bio, China) following the vendor's recommended protocol. RNA libraries were prepared for sequencing using standard Illumina protocols.
Experiment attributes:
GEO Accession: GSM4474405
Links:
Runs: 1 run, 43.8M spots, 12.5G bases, 3.7Gb
Run# of Spots# of BasesSizePublished
SRR1154080043,849,67912.5G3.7Gb2020-04-15

ID:
10560968

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