Clinical Anatomy and Reproductive Medicine Application Institute, Hengyang Medical School, University of South China, Hengyang 421001, China.
Hunan Province Innovative Training Base for Medical Postgraduates, University of South China and Yueyang Women & Children's Medical Center, Yueyang 416000, Hunan, China.
Curr Mol Med. 2023 May 30;23(7):668-677. doi: 10.2174/1566524022666220624105430.
Puberty is initiated from the continuous and growing pulsatile secretion of gonadotropin-releasing hormone (GnRH) in the hypothalamus and then the activation of the hypothalamic-pituitary-gonadal (HPG) axis. Numerous factors involve pubertal initiation, whose abnormality may come from the dysfunction of these regulators. Makorin RING finger protein 3 (MKRN3) inhibits the secretion of GnRH and plays indispensable roles during the development of pubertal onset, and mutations of MKRN3 showed the commonest genetic cause of central precocious puberty (CPP). Recently, growing studies have revealed the functional mechanisms of MKRN3 in the pubertal initiation and the occurrence of CPP. In this review, we mainly summarized the research advances on the roles of MKRN3 in the development of pubertal onset and their underpinning mechanisms, contributing to a better understanding of the precise mechanisms of pubertal initiation and the pathogenesis of CPP.
青春期是由下丘脑持续增长的促性腺激素释放激素(GnRH)脉冲式分泌启动,然后激活下丘脑-垂体-性腺(HPG)轴。许多因素参与青春期的启动,其异常可能来自这些调节因子的功能障碍。泛素连接酶 MKRN3 抑制 GnRH 的分泌,在青春期启动的发育过程中发挥不可或缺的作用,MKRN3 的突变是中枢性性早熟(CPP)最常见的遗传原因。最近,越来越多的研究揭示了 MKRN3 在青春期启动和 CPP 发生中的功能机制。在这篇综述中,我们主要总结了 MKRN3 在青春期启动发育中的作用及其潜在机制的研究进展,有助于更好地理解青春期启动的精确机制和 CPP 的发病机制。