Department of Biochemistry and Functional Genomics, Université de Sherbrooke, Sherbrooke, QC J1K 2R1, Canada.
Int J Mol Sci. 2021 Nov 17;22(22):12418. doi: 10.3390/ijms222212418.
DNA repair is a well-covered topic as alteration of genetic integrity underlies many pathological conditions and important transgenerational consequences. Surprisingly, the ploidy status is rarely considered although the presence of homologous chromosomes dramatically impacts the repair capacities of cells. This is especially important for the haploid gametes as they must transfer genetic information to the offspring. An understanding of the different mechanisms monitoring genetic integrity in this context is, therefore, essential as differences in repair pathways exist that differentiate the gamete's role in transgenerational inheritance. Hence, the oocyte must have the most reliable repair capacity while sperm, produced in large numbers and from many differentiation steps, are expected to carry de novo variations. This review describes the main DNA repair pathways with a special emphasis on ploidy. Differences between and are especially useful to this aim as they can maintain a diploid and haploid life cycle respectively.
DNA 修复是一个备受关注的话题,因为遗传完整性的改变是许多病理状况和重要跨代后果的基础。令人惊讶的是,尽管同源染色体的存在极大地影响了细胞的修复能力,但很少考虑倍性状态。这对于单倍体配子尤其重要,因为它们必须将遗传信息传递给后代。因此,了解在这种情况下监测遗传完整性的不同机制是至关重要的,因为存在区分配子在跨代遗传中作用的修复途径差异。因此,卵子必须具有最可靠的修复能力,而精子则数量众多,并且经过许多分化步骤产生,预计会携带新的变异。本文综述了主要的 DNA 修复途径,特别强调了倍性。 和 之间的差异特别有助于达到这一目的,因为它们分别可以维持二倍体和单倍体的生命周期。