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转录组测序揭示了人类精子样本中存在显著的RNA变异。

Transcriptome sequencing reveals significant RNA variation in human sperm samples.

作者信息

Chen Weiming, Yu Lei, Jia Zhenyu, Zhu Jianguo

机构信息

Guizhou university medical school, South Jiaxiu Rd, Guiyang city, Guizhou province, China.

Guizhou provincial people's hospital, East Zhongshan Rd, Guiyang city, Guizhou province, China.

出版信息

BMC Res Notes. 2025 Jul 12;18(1):288. doi: 10.1186/s13104-025-07356-3.

Abstract

DNA transcription and protein translation are non-coupled for life activities after sperm formation, and if the RNA profile of isolated spermatozoa is resolved, it will help men with epigenetic effects on their offspring and male infertility due to RNA disorders. However, the significance of RNA identity, quantity, and quality in sperm biology and their implications for male fertility are not well understood. We collected 83 semen samples, including with normal sperm motility and with asthenospermia, a condition characterized by reduced sperm motility, for transcriptome sequence. Due to the inherently low RNA content in sperm, only 37 samples were successfully sequenced. Among these, 15 samples met high-quality standards with an RNA Integrity Number (RIN) greater than 6 and a 28 S/18S ratio greater than 0.7, while 22 samples had a RIN between 5 and 6 with a 28 S/18S ratio greater than 0.7. To foster broader research, we have made the RNA sequencing data of these two sets of samples publicly available in the GSA-Human database, under accession numbers HRA006250 and HRA006906, respectively. The data could help develop new algorithms to parse the RNA landscape retained after sperm formation, while potentially discovering new molecular markers of weak asthenospermia.

摘要

精子形成后,DNA转录和蛋白质翻译与生命活动不再耦合。如果能够解析分离出的精子的RNA图谱,将有助于了解男性对其后代的表观遗传影响以及因RNA紊乱导致的男性不育问题。然而,精子生物学中RNA的身份、数量和质量的重要性及其对男性生育能力的影响尚未得到充分理解。我们收集了83份精液样本,包括精子活力正常的样本和弱精子症样本(一种以精子活力降低为特征的病症),用于转录组测序。由于精子中固有的RNA含量较低,只有37个样本成功测序。其中,15个样本达到高质量标准,RNA完整性数值(RIN)大于6且28S/18S比率大于0.7,而22个样本的RIN在5到6之间,28S/18S比率大于0.7。为了促进更广泛的研究,我们已将这两组样本的RNA测序数据分别以登录号HRA006250和HRA006906公开存放在GSA-人类数据库中。这些数据有助于开发新算法来解析精子形成后保留的RNA图谱,同时可能发现弱精子症的新分子标记。

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