Liu Huifang, Kong Xiangxin, Chen Fengling
Department of Endocrinology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Oncotarget. 2017 Jul 18;8(49):85102-85109. doi: 10.18632/oncotarget.19347. eCollection 2017 Oct 17.
Central precocious puberty (CPP) is attributed to the disorder of some trigger factors those can activate the hypothalamic-pituitary-gonadal axis controlled by GnRH neurons. Many recent studies reveal one of those trigger factors, Makorin ring finger protein 3 (Mkrn3), whose loss-of-function mutations are implicated in CPP. Although Mkrn3 contained zinc Ring finger domain is considered as a putative E3 ubiquitin ligase, its actual function is never reported. Here, our results demonstrated that in mice hypothalamus before and when puberty initiated, Mkrn3 expressed the reversed tendency with Nptx1, which is an important secreted protein for neuron development. Furthermore, our data manifested that Mkrn3 interacted and suppressed Nptx1 activity. And the Ring finger domain of Mkrn3 contained was determined to be essential for binding with Nptx1 for its polyubiquitination during the puberty initiation. Our study shed light on the molecular insights into the function of Mkrn3 in the events of puberty initiation.
中枢性性早熟(CPP)归因于一些触发因素的紊乱,这些因素可激活由促性腺激素释放激素(GnRH)神经元控制的下丘脑-垂体-性腺轴。最近的许多研究揭示了其中一种触发因素,即 Makorin 环指蛋白 3(Mkrn3),其功能丧失突变与 CPP 有关。尽管含有锌环指结构域的 Mkrn3 被认为是一种假定的 E3 泛素连接酶,但其实际功能从未被报道过。在这里,我们的结果表明,在小鼠青春期开始前和开始时的下丘脑,Mkrn3 的表达与 Nptx1 呈相反趋势,Nptx1 是一种对神经元发育重要的分泌蛋白。此外,我们的数据表明 Mkrn3 与 Nptx1 相互作用并抑制其活性。并且确定 Mkrn3 所含的环指结构域对于在青春期开始时与 Nptx1 结合以进行其多聚泛素化至关重要。我们的研究揭示了 Mkrn3 在青春期开始事件中功能的分子见解。