Genome-wide association study shows that microtia in Altay sheep is caused by a 76 bp duplication of HMX1
文献类型: 外文期刊
作者: He, S. 1 ; Zhang, Z. 1 ; Sun, Y. 1 ; Ren, T. 1 ; Li, W. 1 ; Zhou, X. 2 ; Michal, J. J. 2 ; Jiang, Z. 2 ; Liu, M. 1 ;
作者机构: 1.Xinjiang Acad Anim Sci, Key Lab Ruminant Genet Breeding & Reprod, Key Lab Anim Biotechnol Xinjiang, Minist Agr,Inst Biotechnol, Urumqi 830026, Xinjiang, Peoples R China
2.Washington State Univ, Dept Anim Sci, Pullman, WA 99164 USA
3.Huazhong Agr Univ, Key Lab Agr Anim Genet Breeding & Reprod, Minist Educ, Wuhan 430070, Hubei, Peoples R China
4.Huazhong Agr Univ, Minist Agr, Key Lab Swine Genet & Breeding, Wuhan 430070, Hubei, Peoples R China
关键词: Short ear; Evolutionarily conserved region; Homobox gene; Ovine
期刊名称:ANIMAL GENETICS ( 影响因子:3.169; 五年影响因子:3.058 )
ISSN: 0268-9146
年卷期: 2020 年 51 卷 1 期
页码:
收录情况: SCI
摘要: Microtia is a congenital malformation of the external ear that can be observed in many species including sheep. However, the genetic basis of microtia still remains unclear. Here, a GWAS was conducted to investigate the genetic basis underlying microtia. A total of 55 samples from 26 microtia and 29 normal animals were genotyped with Illumina OvineHD BeadChip. The strongest significant SNP was identified on OAR6, approximating the evolutionarily conserved region of the HMX1 gene, which is related to congenital malformations of the external ear in other species such as cattle and rats. Sequencing an evolutionarily conserved region surrounding HMX1 revealed a duplication of 76 bp, which is concordant with microtia, suggesting a dominant inheritance mode. Identification of this causal mutation in the HMX1 gene indicates the role of this particular gene in the development of the external ear and provides a genetic marker for selection against microtia.
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