Mutation of spexin2 promotes feeding, somatic growth, adiposity, and insulin resistance in zebrafish

Author:

Zhao Tingting1,Ye Zhifeng1,Liu Yun1,Lin Haoran12,Li Shuisheng1ORCID,Zhang Yong12

Affiliation:

1. State Key Laboratory of Biocontrol, Guangdong Provincial Key Laboratory for Aquatic Economic Animals and Southern Marine Science and Engineering Guangdong Laboratory (Zhuhai), School of Life Sciences, Sun Yat-Sen University, Guangzhou, China

2. Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology, Qingdao, China

Abstract

Spexin2 ( spx2) is a newly identified gene in vertebrates, but its biological functions remain unclear. In this study, we cloned the full-length cDNA of spx2 in zebrafish. The 288-bp open reading frame encodes a protein of 95 amino acids that contains a 14 amino acids mature peptide. Spx2 is highly expressed in brain and testis. Its expression was significantly downregulated in the hypothalamus after feeding treatment and 7 days of food deprivation. Using a zebrafish spx2−/− mutant line, we observed a greater amount of food intake and changes in mRNA levels of feeding factors. We found that, SPX2 acts as a satiety factor that inhibits food intake by downregulating the expression of agouti-related neuropeptide ( agrp). Moreover, spx2 mutant fish exhibited a larger body size, excessive lipid accumulation, and insulin resistance. Taken together, our results revealed that SPX2 functions as a satiety factor involved in energy metabolic regulation in zebrafish.

Funder

Guangdong Basic and Applied Basic Research Foundation

Innovation Group Project of Southern Marine Science and Engineering Guangdong Laboratory

Science and Technology Planning Project of Guangzhou

Publisher

American Physiological Society

Subject

Physiology (medical),Physiology

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