Priority Research Centre for Reproductive Science, Faculty of Science and Faculty of Health and Medicine, University of Newcastle, Callaghan, New South Wales 2308, Australia; email:
Hunter Medical Research Institute, New Lambton Heights, New South Wales 2305, Australia.
Annu Rev Genet. 2020 Nov 23;54:1-24. doi: 10.1146/annurev-genet-112618-043617. Epub 2020 Jul 14.
Spermatogonial stem cells (SSCs) are generally characterized by excellent DNA surveillance and repair, resulting in one of the lowest spontaneous mutation rates in the body. However, the barriers to mutagenesis can be overwhelmed under two sets of circumstances. First, replication errors may generate age-dependent mutations that provide the mutant cells with a selective advantage, leading to the clonal expansions responsible for dominant genetic diseases such as Apert syndrome and achondroplasia. The second mechanism centers on the vulnerability of the male germline to oxidative stress and the induction of oxidative DNA damage in spermatozoa. Defective repair of such oxidative damage in the fertilized oocyte results in the creation of mutations in the zygote that can influence the health and well-being of the offspring. A particular hot spot for such oxidative attack on chromosome 15 has been found to align with several mutations responsible for paternally mediated disease, including cancer, psychiatric disorders, and infertility.
精原干细胞(SSCs)的特点是具有出色的 DNA 监测和修复能力,因此其自发突变率在体内处于较低水平。然而,在两种情况下,诱变的障碍可能会被克服。首先,复制错误可能会产生与年龄相关的突变,为突变细胞提供选择性优势,导致负责显性遗传疾病(如尖颅并指综合征和软骨发育不全)的克隆扩张。第二种机制主要集中在男性生殖细胞对氧化应激的脆弱性以及精子中氧化 DNA 损伤的诱导上。在受精卵中,这种氧化损伤的修复缺陷会导致胚胎中产生突变,从而影响后代的健康和幸福。在染色体 15 上,这种氧化攻击的一个特定热点与几个导致父系介导疾病的突变有关,包括癌症、精神障碍和不育。