鱼精蛋白失调患者鱼精蛋白基因5′和3′非编码区遗传变异的鉴定。

Sue Hammoud, Benjamin R Emery, Vincent W Aoki, Douglas T Carrell
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引用次数: 16

摘要

精子核精蛋白比率(P1/P2)的失调已被证明与人类男性因素不育有关,但这种异常蛋白表达的原因尚未确定。最近的研究表明,鱼精蛋白基因序列的编码区几乎没有遗传变异。然而,这些研究并没有研究这些基因的5'或3'非编码区域的突变,这些突变可能解释了蛋白质转录或翻译调节的变化。为了确定这些非编码区域的遗传变异是否可能导致鱼精蛋白的异常表达,我们对鱼精蛋白1 (P1)和鱼精蛋白2 (P2)基因的5'和3'非翻译区域(UTRs)进行了测序,这些人群包括鱼精蛋白失调的不育男性、鱼精蛋白比例正常的不育男性以及来自犹他州遗传参考项目(UGRP)的无亲缘关系的可生育男性。该分析鉴定了14个单核苷酸多态性(SNPs),其中13个是P1和P2的utr中的新snp,并验证了P2 5'区存在可变长度重复(VLR) GAn。SNP频率和VLR等位基因频率在人群间不具有统计学意义,但在鱼精蛋白2的3′UTR中发现的一个SNP在异常鱼精蛋白患者中频率较低,而在确认鱼精蛋白比例正常的男性和已知生育能力的供者中完全不存在。综上所述,在鱼精蛋白基因和非翻译区域中已经报道了一些snp,然而,这些基因变异似乎并不是造成鱼精蛋白缺乏的原因。因此,鱼精蛋白异常表达的潜在原因可能是候选生精转录/翻译调节因子、翻译后修饰因子或影响睾丸环境的尚未确定因素的异常。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of genetic variation in the 5' and 3' non-coding regions of the protamine genes in patients with protamine deregulation.

Deregulation of sperm nuclear protamine ratio (P1/P2) has been shown to correlate with male factor infertility in humans, but the cause of this abnormal protein expression has yet to be identified. Recent studies have shown that there is little genetic variability in the coding regions of either of the protamine gene sequences. However, these studies did not investigate the 5' or 3' non-coding regions of these genes for mutations that might account for changes in the transcriptional or translational regulation of the protamines. In an effort to determine if genetic variation in these non-coding regions may account for aberrant protamine expression, we have sequenced the 5' and 3' untranslated regions (UTRs) of both protamine 1 (P1) and protamine 2 (P2) genes in a population of infertile men with protamine deregulation, men presenting for infertility work-up with normal protamine ratios, and a population of unrelated, fertile men from the Utah Genetic Reference Project (UGRP). This analysis has identified 14 single nucleotide polymorphisms (SNPs), of which 13 were novel SNPs in the UTRs of P1 and P2, and verified the existence of a variable length repeat (VLR), GAn, in the P2 5' region. The SNP frequencies and VLR allelic frequencies did not achieve statistical significance between the populations, however, one of the SNPs identified in the 3' UTR of protamine 2 was found at a low frequency in the abnormal protamine patients, but was completely absent in men with verified normal protamine ratio and donors of known fertility. In conclusion, a number of SNPs have been reported in the protamine genes and the untranslated regions, however, these gene variants do not appear to be responsible for protamine deficiency. Hence, the underlying cause for aberrant protamine expression may possibly be due to abnormalities in candidate spermatogenic transcriptional/translational regulators, post-translational modifiers, or as-of-yet unidentified factors affecting the testicular environment.

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