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Makorin rings the kisspeptin bell to signal pubertal initiation

机译:Makorin戒指吻疱疹以信号发育青春期

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摘要

The signals maintaining quiescence of the reproductive endocrine axis during childhood before its reawakening at puberty had been enigmatic. Studies in patients with abnormal puberty have illuminated the identity of the signals; kisspeptin has emerged as a major stimulator of puberty, and makorin RING finger protein 3 (MKRN3) as an inhibitory signal that prevents premature initiation of puberty. In this issue of the JCI, Abreu et al. investigated the mechanism by which MKRN3 regulates pubertal onset. The authors found that a reduction in MKRN3 alleviated the constraint on kisspeptin-expressing neurons to allow pubertal initiation, a phenomenon observed across species, including nonhuman primates. Further, the ubiquitinase activity of MKRN3 required its RING finger domain, in order to repress the promoter activity of genes encoding kisspeptin and neurokinin B. These data advance our understanding of the regulation of kisspeptin-expressing neurons by MKRN3 to initiate puberty.
机译:在青春期重新制作之前,在儿童期间保持生殖内分泌轴的静态的信号一直是神秘的。异常青春期患者的研究阐明了信号的身份; Kisspeptin已成为青春期的主要刺激器,以及Makorin Ring Finger Protein 3(MKRN3),作为抑制信号,可防止青春期过早启动。在这个问题的JCI,Abreu等。调查MKRN3调节福伯塔尔发病的机制。作者发现,MKRN3的减少减轻了对表达吻表达的神经元的约束,以允许普别培养开始,在包括非人的灵长类动物的物种中观察到的现象。此外,MKRN3的泛素酶活性需要其环形手指结构域,以抑制编码Kisspeptin和Neurokinin B的基因的启动子活性。这些数据通过MKRN3引发了MKRN3引发青春期的对吻表达的神经元的调节。

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