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不孕女性中的白血病抑制因子基因突变

Leukaemia inhibitory factor gene mutations in infertile women.

作者信息

Giess R, Tanasescu I, Steck T, Sendtner M

机构信息

Department of Neurology (Clinical Research Group), Julius-Maximilians-University of Würzburg, Josef Schneider Strabetae 11, 97080 Würzburg, Germany.

出版信息

Mol Hum Reprod. 1999 Jun;5(6):581-6. doi: 10.1093/molehr/5.6.581.

Abstract

The glycoprotein leukaemia inhibitory factor (LIF) is produced by the endometrium and is involved in the control of implantation. In women with unexplained infertility reduced uterine concentrations of LIF have been reported. Studies with mice lacking a functional LIF gene have shown that the LIF protein is essential for implantation of the embryo. We have developed a method for screening of gene mutations in the coding region and critical regulatory regions of the LIF gene. Thus we could screen nulligravid infertile women (n = 74), fertile controls (n = 75) and as a second unrelated control group, neurological patients (n = 131) for LIF gene mutations. In infertile women, three heterozygous point mutations have been identified: one in close proximity to the start codon of exon 1 and two mutations in exon 3. These correspond to regions of the LIF protein which are thought to be highly important for interaction with the LIF receptor and thus lead to reduced biological activity of the LIF protein. Only one point mutation/polymorphism in the non-coding region between exon 2 and 3 was found in the control groups. Our results suggest that heterozygosity for a LIF gene mutation could give rise to decreased availability or biological activity of LIF in the uterus and cause implantation failure. Thus the mutations identified in our study could be responsible for infertility in a subgroup of nulligravid women.

摘要

糖蛋白白血病抑制因子(LIF)由子宫内膜产生,参与着床调控。据报道,不明原因不孕症女性的子宫LIF浓度降低。对缺乏功能性LIF基因的小鼠进行的研究表明,LIF蛋白对胚胎着床至关重要。我们开发了一种方法,用于筛查LIF基因编码区和关键调控区的基因突变。因此,我们可以筛查未孕不育女性(n = 74)、有生育能力的对照组(n = 75)以及作为第二个不相关对照组的神经科患者(n = 131)的LIF基因突变情况。在不育女性中,已鉴定出三个杂合点突变:一个靠近外显子1的起始密码子,另外两个在外显子3中。这些突变对应于LIF蛋白中被认为对与LIF受体相互作用非常重要的区域,从而导致LIF蛋白的生物活性降低。在对照组中,仅在外显子2和3之间的非编码区发现了一个点突变/多态性。我们的结果表明,LIF基因突变的杂合性可能导致子宫中LIF的可用性或生物活性降低,并导致着床失败。因此,我们研究中鉴定出的突变可能是未孕女性亚组中不孕症的原因。

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