USTC-SDJH Joint Center for Human Reproduction and Genetics, The CAS Key Laboratory of Innate Immunity and Chronic Diseases, Hefei National Laboratory for Physical Sciences at Microscale, School of Life Sciences, CAS Center for Excellence in Molecular Cell Science, University of Science and Technology of China (USTC), Collaborative Innovation Center of Genetics and Development, Hefei, 230027, Anhui, China.
Sci Rep. 2018 Mar 21;8(1):4975. doi: 10.1038/s41598-018-23176-x.
There are more than 2300 genes that are predominantly expressed in mouse testes. The role of hundreds of these genes has been studied in mouse spermatogenesis but still there are many genes whose function is unknown. Gene knockout (KO) strategy in mice is widely used for in vivo study of gene function. The present study was designed to explore the function of the four genes: Tex37, Ccdc73, Prss55 and Nxt2, which were evolutionarily conserved in eutherians. We found that these genes had a testis-enriched expression pattern in mice except Nxt2. We knocked out these genes by CRISPR/Cas9 individually and found that all the KO mice had normal fertility with no detectable difference in testis/body weight ratios, epididymal sperm counts, as well as testicular and epididymal histology from wild type mice. Although these genes are evolutionarily conserved in eutherians including human and mouse, they are not individually essential for spermatogenesis, testis development and male fertility in mice in laboratory conditions. Our report of these fertile KO data could avoid the repetition and duplication of efforts which will help in prioritizing efforts to focus on genes that are indispensable for male reproduction.
有超过 2300 个基因主要在小鼠睾丸中表达。其中数百个基因在小鼠精子发生过程中的作用已经得到了研究,但仍有许多基因的功能未知。基因敲除(KO)策略在小鼠中被广泛用于基因功能的体内研究。本研究旨在探索 Tex37、Ccdc73、Prss55 和 Nxt2 这四个在真兽类中进化保守的基因的功能。我们发现这些基因在小鼠中表现出睾丸富集的表达模式,除了 Nxt2。我们通过 CRISPR/Cas9 单独敲除了这些基因,发现所有 KO 小鼠的生育能力正常,睾丸/体重比、附睾精子计数以及睾丸和附睾组织学与野生型小鼠没有明显差异。尽管这些基因在包括人类和小鼠在内的真兽类中是进化保守的,但在实验室条件下,它们对于精子发生、睾丸发育和雄性生育力并不是必不可少的。我们报告这些具有生育能力的 KO 数据可以避免重复和重复的努力,这将有助于优先考虑对雄性生殖不可或缺的基因的研究。