Leptin and Its Signaling Are Not Involved in Zebrafish Puberty Onset

生物 瘦素 内科学 小鼠苗条素受体 内分泌学 斑马鱼 青春期延迟 突变体 促性腺激素减退症 体细胞 表型 肥胖 激素 遗传学 基因 医学
作者
Zhe Hu,Cheng Jiang,Weiting Chen,Queenie Wing-Lei Wong,Wei Ge
出处
期刊:Biology of Reproduction [Oxford University Press]
卷期号:106 (5): 928-942 被引量:11
标识
DOI:10.1093/biolre/ioac005
摘要

Leptin is a peptide hormone secreted from the adipose tissues and its signaling plays a central role in metabolic regulation of growth, especially on fat mass. In addition, leptin is also involved in regulating reproduction in mammals. In teleosts, there are two leptin ligands (lepa and lepb) and one cognate leptin receptor (lepr); however, their functions are still elusive. In this study, we created null-function mutants for lepa, lepb and lepr in zebrafish using CRISPR/Cas9 method and analyzed their phenotypes with emphasis on puberty onset, one major function widely reported for leptin in mammals. We demonstrated that the loss of leptin ligands or their receptor resulted in no obesity from prepubertal stage to adulthood. We then focused on leptin involvement in controlling puberty onset. We first confirmed the somatic threshold for puberty onset in females and proposed a criterion and somatic threshold for male puberty onset. We examined gonadal development and sex maturation in different genotypic combinations including single mutants (lepa-/-, lepb-/- and lepr-/-), double mutants (lepa-/-;lepb-/-) and triple mutants (lepa-/-;lepb-/-;lepr-/-). Our results showed that once the fish reached the thresholds, the siblings of all genotypes displayed comparable gonadal development in both sexes without obvious signs of changed puberty onset. In conclusion, this comprehensive genetic study on the lep-lepr system demonstrated that in contrast to its counterpart in mammals, leptin system plays little role in controlling growth and reproduction especially puberty onset in zebrafish.
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