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Cloning, Expression Analysis and SNP Screening of the kiss1 Gene in Male Schizothorax biddulphi

文献类型： 外文期刊

作者： Nie, Zhulan 1 ; Zhao, Nianhua 1 ; Zhao, He 1 ; Fu, Zhengyi 5 ; Ma, Zhenhua 5 ; Wei, Jie 1 ;

作者机构： 1.Tarim Univ, Coll Life Sci & Technol, Alaer 843300, Peoples R China

2.Xinjiang Prod & Construct, Key Lab Tarim Anim Husb Sci & Technol, Alaer 843300, Peoples R China

3.Tarim Univ, State Kay Lab Breeding Base Protect & Utilizat Bio, Alaer 843300, Peoples R China

4.Tarim Univ, Minist Sci & Technol, Alaer 843300, Peoples R China

5.Chinese Acad Fishery Sci, South China Sea Fisheries Res Inst, Trop Aquaculture Res & Dev Ctr, Sanya 572018, Peoples R China

6.Flinders Univ S Australia, Coll Sci & Engn, Adelaide, SA 5001, Australia

关键词： association analysis; gene expression; kisspeptin; polymorphism; Schizothorax biddulphi

期刊名称：GENES （ 影响因子：3.5； 五年影响因子：3.9 ）

ISSN：

年卷期： 2023 年 14 卷 4 期

页码：

收录情况： SCI

摘要： Schizothorax biddulphi is an endemic fish distributed only in southern Xinjiang, China. Due to overfishing, water conservancy facilities, and other factors, as well as inherent biological limitations, resource recovery is quite difficult. For endangered fish with slow growth, late sexual maturity, and insufficient natural population supplementation, large-scale artificial reproduction and breeding are important for restoring resources. Therefore, it is urgent to optimize the reproductive regulation methods of the fish. The kiss1 gene is a key regulator of the reproductive regulation cascade, and identifying and analyzing the role of kiss1 are important for further elucidating the reproductive mechanism of S. biddulphi. To understand the characteristics of the kiss1 of S. biddulphi, the full-length cDNA sequence of kiss1 was obtained in this study, and its tissue expression specificity and association with phenotypic traits were analyzed in male fish. The full-length cDNA sequence of kiss1 in S. biddulphi was 658 bp, with an ORF of 327 bp, and encoded a 108-amino acid, unstable protein. Homology results indicated that kiss1 was highly conserved. qPCR showed kiss1 expression in different tissues in male S. biddulphi, with the highest expression in the gonads, followed by muscle, and significantly lower expression in the swim bladder, pituitary gland, heart, hypothalamus, gill, fin, liver, eye, and mid-kidney. qPCR revealed three SNP loci in the exonic region of kiss1. The c.3G>T locus was significantly correlated (p < 0.05) with gonad mass and the maturation coefficient in S. biddulphi. These results will help uncover the reproductive endocrinology network of S. biddulphi, improve artificial breeding technology for fish, and unveil new directions for breeding excellent strains of S. biddulphi and molecular marker-assisted breeding.

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