Back to Search Start Over

Selection of Cashmere Fineness Functional Genes by Translatomics.

Authors :
Zhang, Yu
Zhang, Dongyun
Xu, Yanan
Qin, Yuting
Gu, Ming
Cai, Weidong
Bai, Zhixian
Zhang, Xinjiang
Chen, Rui
Sun, Yingang
Wu, Yanzhi
Wang, Zeying
Source :
Frontiers in Genetics; 1/12/2022, Vol. 12, p1-17, 17p
Publication Year :
2022

Abstract

Cashmere fineness is an important index to evaluate cashmere quality. Liaoning Cashmere Goat (LCG) has a large cashmere production and long cashmere fiber, but its fineness is not ideal. Therefore, it is important to find genes involved in cashmere fineness that can be used in future endeavors aiming to improve this phenotype. With the continuous advancement of research, the regulation of cashmere fineness has made new developments through high-throughput sequencing and genome-wide association analysis. It has been found that translatomics can identify genes associated with phenotypic traits. Through translatomic analysis, the skin tissue of LCG sample groups differing in cashmere fineness was sequenced by Ribo-seq. With these data, we identified 529 differentially expressed genes between the sample groups among the 27197 expressed genes. From these, 343 genes were upregulated in the fine LCG group in relation to the coarse LCG group, and 186 were downregulated in the same relationship. Through GO enrichment analysis and KEGG enrichment analysis of differential genes, the biological functions and pathways of differential genes can be found. In the GO enrichment analysis, 491 genes were significantly enriched, and the functional region was mainly in the extracellular region. In the KEGG enrichment analysis, the enrichment of the human papillomavirus infection pathway was seen the most. We found that the COL6A5 gene may affect cashmere fineness. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16648021
Volume :
12
Database :
Complementary Index
Journal :
Frontiers in Genetics
Publication Type :
Academic Journal
Accession number :
154665577
Full Text :
https://doi.org/10.3389/fgene.2021.775499