基因组测序项目揭示了哺乳动物促性腺激素释放激素 II 系统的新奥秘。

IF 3.3 4区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Kevin Morgan, Robert P Millar
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引用次数: 0

摘要

II型促性腺激素释放激素(GnRH-II)首先在鸡(Gallus gallus)脑中被发现,随后被证明存在于许多脊椎动物体内。事实上,从远洋鱼类到哺乳动物,它的结构在脊椎动物的进化过程中始终保持不变,这表明它具有至关重要的功能。然而,其功能意义在很大程度上还未被探索。比较内分泌学的研究表明,GnRH-II 系统在哺乳动物物种中具有不同的功能。完整的 GnRH-II 神经肽和受体基因(GnRH2 和 GnRH 受体 2 GnRHR2)存在于狨猴(Callithrix jacchus)、麝香鼩(Suncus murinus)和猪(Sus scrofa)中。然而,在其他物种中,这些基因中的一个或另一个或两个都失活了,在这些物种中,影响 GnRH2 神经肽和/或 II 型 GnRHR 外显子的突变或残余保留在保守的基因组位点中。DNA 测序项目的新数据有助于对这些基因的物种特异性变异进行广泛分析。在这里,我们描述了 GnRH2 和 GnRHR2 基因,这些基因横跨 21 个分类目,包括灵长目、山地目、雌雄异体目、啮齿目、长尾目、有齿目、食肉目、短吻目、长足目、脊索动物门、非洲动物门、侏罗纪动物门和有袋动物门的约 140 个物种。GnRH2 和 GnRHR2 的完整编码外显子出现在猴、树鼩、鼩鼱、鼹鼠、刺猬、几种啮齿类动物(degu、袋鼠、袖珍鼠)、猪、猯和疣猪、骆驼和羊驼、熊、威德尔海豹、鬣狗、大象、土豚和有袋类动物中。影响 GnRH2 和 GnRHR2 的非活化突变(有些位于外显子内的保守位点)出现在灵长类、大多数啮齿类、袋鼬、牛科、鲸类、猫科、犬科和其他食肉目动物、穿山甲、大多数蝙蝠、犰狳、刷尾和针鼹等物种中。功能性 GnRH-II 系统似乎保留在哺乳动物的几个分类科中,但完整的保留并没有扩展到整个分类目。确定内源性 GnRH-II 神经肽在不同哺乳动物体内的运作方式,可能有助于深入了解其在大脑中的作用,特别是与 I 型 GnRH 系统不同,它在中脑而非下丘脑中表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genome sequencing projects reveal new insights into the mammalian Gonadotropin-releasing Hormone II system.

The type II gonadotropin-releasing hormone (GnRH-II) was first discovered in chicken (Gallus gallus) brain and then shown to be present in many vertebrates. Indeed, its structure is conserved unchanged throughout vertebrate evolution from teleost fish through to mammals suggesting a crucial function. Yet the functional significance has been largely unexplored. Studies in comparative endocrinology show that the GnRH-II system is differentially functional in mammalian species. Intact GnRH-II neuropeptide and receptor genes (GnRH2 and GnRH receptor 2 GnRHR2) occur in marmoset monkeys (Callithrix jacchus), musk shrews (Suncus murinus) and pigs (Sus scrofa). However, one or other or both of these genes are inactivated in other species, where mutations or remnants affecting GnRH2 neuropeptide and/or type II GnRHR exons are retained in conserved genomic loci. New data from DNA sequencing projects facilitate extensive analysis of species-specific variation in these genes. Here, we describe GnRH2 and GnRHR2 genes spanning a collection of 21 taxonomic orders, encompassing around 140 species from Primates, Scandentia, Eulipotyphla, Rodentia, Lagomorpha, Artiodactyla, Carnivora, Perissodactyls, Pholidota, Chiroptera, Afrotheria, Xenarthra and Marsupialia. Intact coding exons for both GnRH2 and GnRHR2 occur in monkeys, tree shrews, shrews, moles, hedgehogs, several rodents (degu, kangaroo-rat, pocket mouse), pig, pecarry and warthog, camels and alpaca, bears, Weddell seal, hyena, elephant, aardvark and marsupials. Inactivating mutations affecting GnRH2 and GnRHR2, some located at conserved sites within exons, occur in species of primates, most rodents, lagomorphs, bovidae, cetaceans, felidae, canidae and other carnivora, pangolins, most bats, armadillo, brushtail and echidna. A functional GnRH-II system appears retained within several taxonomic families of mammals, but intact retention does not extend to whole taxonomic orders. Defining how endogenous GnRH-II neuropeptide operates in different mammals may afford functional insight into its actions in the brain, especially as, unlike the type I GnRH system, it is expressed in the mid brain and not the hypothalamus.

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来源期刊
Journal of Neuroendocrinology
Journal of Neuroendocrinology 医学-内分泌学与代谢
CiteScore
6.40
自引率
6.20%
发文量
137
审稿时长
4-8 weeks
期刊介绍: Journal of Neuroendocrinology provides the principal international focus for the newest ideas in classical neuroendocrinology and its expanding interface with the regulation of behavioural, cognitive, developmental, degenerative and metabolic processes. Through the rapid publication of original manuscripts and provocative review articles, it provides essential reading for basic scientists and clinicians researching in this rapidly expanding field. In determining content, the primary considerations are excellence, relevance and novelty. While Journal of Neuroendocrinology reflects the broad scientific and clinical interests of the BSN membership, the editorial team, led by Professor Julian Mercer, ensures that the journal’s ethos, authorship, content and purpose are those expected of a leading international publication.
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