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Genomic analyses of wild argali, domestic sheep, and their hybrids provide insights into chromosome evolution, phenotypic variation, and germplasm innovation

Authors :
Xin Li
San-Gang He
Wen-Rong Li
Ling-Yun Luo
Ze Yan
Dong-Xin Mo
Xing Wan
Feng-Hua Lv
Ji Yang
Ya-Xi Xu
Juan Deng
Qiang-Hui Zhu
Xing-Long Xie
Song-Song Xu
Chen-Xi Liu
Xin-Rong Peng
Bin Han
Zhong-Hui Li
Lei Chen
Jian-Lin Han
Xue-Zhi Ding
Renqing Dingkao
Yue-Feng Chu
Jin-Yan Wu
Li-Min Wang
Ping Zhou
Ming-Jun Liu
Meng-Hua Li
Source :
Genome Research. 32:1669-1684
Publication Year :
2022
Publisher :
Cold Spring Harbor Laboratory, 2022.

Abstract

Understanding the genetic mechanisms of phenotypic variation in hybrids between domestic animals and their wild relatives may aid germplasm innovation. Here, we report the high-quality genome assemblies of a male Pamir argali (O. ammon polii, 2n = 56), a female Tibetan sheep (O. aries, 2n = 54), and a male hybrid of Pamir argali and domestic sheep, and the high-throughput sequencing of 425 ovine animals, including the hybrids of argali and domestic sheep. We detected genomic synteny between Chromosome 2 of sheep and two acrocentric chromosomes of argali. We revealed consistent satellite repeats around the chromosome breakpoints, which could have resulted in chromosome fusion. We observed many more hybrids with karyotype 2n = 54 than with 2n = 55, which could be explained by the selfish centromeres, the possible decreased rate of normal/balanced sperm, and the increased incidence of early pregnancy loss in the aneuploid ewes or rams. We identified genes and variants associated with important morphological and production traits (e.g., body weight, cannon circumference, hip height, and tail length) that show significant variations. We revealed a strong selective signature at the mutation (c.334C > A, p.G112W) in TBXT and confirmed its association with tail length among sheep populations of wide geographic and genetic origins. We produced an intercross population of 110 F2 offspring with varied number of vertebrae and validated the causal mutation by whole-genome association analysis. We verified its function using CRISPR-Cas9 genome editing. Our results provide insights into chromosomal speciation and phenotypic evolution and a foundation of genetic variants for the breeding of sheep and other animals.

Subjects

Subjects :
Genetics
Genetics (clinical)

Details

ISSN :
15495469 and 10889051
Volume :
32
Database :
OpenAIRE
Journal :
Genome Research
Accession number :
edsair.doi.dedup.....648a9964142e8336faac9213ba75757e
Full Text :
https://doi.org/10.1101/gr.276769.122