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沧海一粟:GNRH1 突变是孤立性 GnRH 缺乏症的罕见病因。

A needle in a haystack: mutations in GNRH1 as a rare cause of isolated GnRH deficiency.

机构信息

Harvard Reproductive Sciences Center and Reproductive Endocrine Unit of the Department of Medicine, Massachusetts General Hospital, Boston, MA 02114, United States.

出版信息

Mol Cell Endocrinol. 2011 Oct 22;346(1-2):51-6. doi: 10.1016/j.mce.2011.06.013. Epub 2011 Jun 22.

Abstract

GNRH1, the human gene that gives rise to GnRH, has long been an obvious candidate gene for idiopathic hypogonadotropic hypogonadism, particularly because the hpg mouse, a mouse model of isolated hypogonadotropic hypogonadism, carries a deletion that disrupts Gnrh1. In 2009, 25 years after the sequence of human GNRH1 was initially determined, two groups independently reported homozygous frameshift mutations in GNRH1 in patients with idiopathic hypogonadotropic hypogonadism. In two additional families, heterozygous GNRH1 mutations segregated with reproductive disorders. In the first family, the mutation occurred alone in five female subjects with idiopathic hypogonadotropic hypogonadism, whereas in the second it co-existed with a mutation in NR0B1/DAX1 in two female subjects with delayed puberty. While hemizygous mutations the X-linked NR0B1 are a well-known cause of hypogonadotropic hypogonadism and adrenal hypoplasia in male patients, heterozygous female carriers are generally asymptomatic. Thus, mutations in GNRH1 have been associated with both mild and severe forms of GnRH deficiency, and may work in combination with other gene mutations to produce GnRH-deficient phenotypes.

摘要

GNRH1 是人类 GnRH 的基因,长期以来一直是特发性低促性腺激素性性腺功能减退症的候选基因,尤其是因为 hpg 小鼠,一种孤立性低促性腺激素性性腺功能减退症的小鼠模型,携带破坏 Gnrh1 的缺失。2009 年,在人类 GNRH1 序列最初确定 25 年后,两组独立报道了特发性低促性腺激素性性腺功能减退症患者 GNRH1 的纯合移码突变。在另外两个家族中,杂合 GNRH1 突变与生殖障碍分离。在第一个家族中,该突变单独发生在五名患有特发性低促性腺激素性性腺功能减退症的女性受试者中,而在第二个家族中,该突变与两个青春期延迟的女性受试者中的 NR0B1/DAX1 突变共存。虽然 X 连锁 NR0B1 的半合子突变是男性患者低促性腺激素性性腺功能减退症和肾上腺发育不全的已知原因,但杂合子女性携带者通常无症状。因此,GNRH1 突变与 GnRH 缺乏的轻度和重度形式有关,并且可能与其他基因突变一起作用以产生 GnRH 缺乏表型。

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