正常精子和弱精子男性精子中过渡蛋白1,2精子特异性连接蛋白h1样蛋白转录物的定量评估。

Piotr Jedrzejczak, Bartosz Kempisty, Artur Bryja, M Mostowska, Magdalena Depa-Martynow, Leszek Pawelczyk, Pawel Piotr Jagodzinski
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引用次数: 42

摘要

精细胞特异性连接蛋白h1样蛋白(HILS1)、过渡蛋白1和2 (TNP1和TNP2)以及精蛋白1和2 (PRM1和PRM2)在精子发生过程中有助于精细胞染色质的密集堆积。我们评估了正常精子和弱精子男性分离的精子中HILS1、TNP1和TNP2转录物的水平。正常精子(n = 70)和弱精子(n = 100)供体的人类射精通过不连续Percoll密度梯度离心纯化。按照Chomczynski和Sacchi方法从精子中分离RNA,用DNase I处理后反转录为cDNA。通过实时定量(RQ-PCR) SYBR green I分析对HILS1、TNP1和TNP2转录本进行定量分析。我们发现,与正常精子男性相比,弱精子男性精子中HILS1、TNP1和TNP2转录物的水平显著降低。我们的观察表明,HILS1、TNP1和TNP2转录物的减少可能与弱精子症有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantitative assessment of transition proteins 1, 2 spermatid-specific linker histone H1-like protein transcripts in spermatozoa from normozoospermic and asthenozoospermic men.

Spermatid-specific linker histone H1-like protein (HILS1), transition proteins 1 and 2 (TNP1 and TNP2), and protamines 1 and 2 (PRM1 and PRM2) contribute to considerable dense packing of spermatid chromatin during spermiogenesis. We evaluated the HILS1, TNP1, and TNP2 transcript levels in spermatozoa isolated from normozoospermic and asthenozoospermic men. Human ejaculates from normozoospermic (n = 70) and asthenozoospermic (n = 100) donors were purified by centrifugation through a discontinuous Percoll density gradient. RNA was isolated from spermatozoa according to the Chomczynski and Sacchi method, treated with DNase I and reverse-transcribed into cDNA. Quantitative analysis of HILS1, TNP1, and TNP2 transcripts was performed by real-time quantitative (RQ-PCR) SYBR green I analysis. We found significantly lower levels of HILS1, TNP1, and TNP2 transcripts in spermatozoa from asthenozoospermic men compared to normozoospermic men. Our observations suggest that a reduction in HILS1, TNP1, and TNP2 transcripts may be associated with asthenozoospermia.

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