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

Author:

Nie Zhulan123,Zhao Nianhua123,Zhao He123,Fu Zhengyi45,Ma Zhenhua45ORCID,Wei Jie123ORCID

Affiliation:

1. College of Life Sciences and Technology, Tarim University, Alaer 843300, China

2. Key Laboratory of Tarim Animal Husbandry Science and Technology, Xinjiang Production & Construction, Alaer 843300, China

3. State Kay Laboratory Breeding Base for the Protection and Utilization of Biological Resources in Tarim Basin Co-Funded by Xinjiang Corps and the Ministry of Science and Technology, Tarim University, Alaer 843300, China

4. Tropical Aquaculture Research and Development Center, South China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Sanya 572018, China

5. College of Science and Engineering, Flinders University, Adelaide, SA 5001, Australia

Abstract

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.

Funder

National Natural Science Foundation of Chin

Young and Middle-aged Science and Technology Innovation Leading Talent Program Project of Xinjiang Production and Construction Corps

President’s Fund of Tarim University-Germplasm Resources and Genetic Breeding of Schizothorax in Southern Xinjiang Innovative Research Team Project

The Third Xinjiang Integrated Scientific Expedition Project

United Fund of the Ocean University of China and Tarim University

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

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