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SRX9390117: GSM4871466: LncRNA-TC2; Gallus gallus; RNA-Seq
1 ILLUMINA (Illumina HiSeq 4000) run: 56.3M spots, 16.8G bases, 4.8Gb downloads

Submitted by: NCBI (GEO)
Study: Comprehensive analysis of coding and non-Coding RNA transcriptomes related to hypoxic adaptation in the Tibetan chickens
show Abstracthide Abstract
Tibetan chicken has a suite of adaptive features to tolerate the high-altitude hypoxic environment as a unique native breed in Qinghai-Tibet Plateau of China. Increasing evidence suggests that long non-coding RNAs (lncRNAs) and microRNAs (miRNAs) have roles in hypoxic adaptation of high-altitude animals, though their exact contributions remain unclear. This study aims to uncover the global landscape of mRNAs, lncRNAs and miRNAs using transcriptome sequencing so as to construct a regulatory network of competing endogenous RNAs (ceRNAs) provide a new sight for the hypoxic adaptation of Tibetan chicken embryos. In the study, 354 differentially expressed mRNAs (DEGs), 389 differentially expressed lncRNAs (DELs) and 73 differentially expressed miRNAs (DEMs) were identified between Tibetan (TC) and Chahua chicken (CH). The functional analysis showed that several important DEMs and their targets of DELs and DEMs are involved in angiogenesis (include blood vessel development and blood circulation) and energy metabolism (include glucose, carbohydrate and lipid metabolism). The ceRNA network was then constructed with the predicted pairs of DEGs-DEMs-DELs which further revealed regulatory roles of these differentially expressed RNAs in hypoxic adaptation of Tibetan chicken. Overall design: Chorioallantoic membrane (CAM) of embryos coding and non-coding RNA profiles of 11-day old Tibetan chickens (TCs) and Chahua chickens (CHs) were generated by deep sequencing, in triplicate.
Sample: LncRNA-TC2
SAMN16582154 • SRS7609416 • All experiments • All runs
Organism: Gallus gallus
Library:
Instrument: Illumina HiSeq 4000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Chorioallantoic membrane tissues were removed, frozen on liquid nitrogen, and total RNA was harvested using Trizol reagent. Illumina HiSeq RNA Sample Prep Kit (Cat.#RS-122-2002; Illumina, San Diego, CA, USA) was used with 1 ug of total RNA for the construction of sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols
Experiment attributes:
GEO Accession: GSM4871466
Links:
Runs: 1 run, 56.3M spots, 16.8G bases, 4.8Gb
Run# of Spots# of BasesSizePublished
SRR1292590156,309,58116.8G4.8Gb2020-10-29

ID:
12257766

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