, Chandigarh, India.
Curr Genet. 2019 Dec;65(6):1301-1306. doi: 10.1007/s00294-019-00991-x. Epub 2019 May 10.
This review elaborates on the findings of a new report which possibly resolves the biochemical nature of a novel type of DNA imprint as ribonucleotide and the mechanism of its formation during cell differentiation in fission yeast. The process of mating-type switching in fission yeast, Schizosaccharomyces pombe, displays characteristics of a typical mammalian stem cell lineage, wherein a cell divides to produce an identical cell and a differentiated cell after every two cell divisions. This developmental asymmetry has been ascribed to play a role in generation of a DNA strand-specific imprint at the mat1 locus during lagging strand synthesis and its segregation to one of the two daughter cells by the process of asymmetric, semi-conservative DNA replication. The nature of this imprint and mechanisms of its generation have been a subject of research and debate. A recent report by Singh et al. (Nucleic Acids Res 47:3422-3433. https://doi.org/10.1093/nar/gkz092 , 2019) provides compelling evidence in support of a ribonucleotide as the imprint moiety within the mat1 DNA and demonstrates the role of Mcm10/Cdc23, an important, evolutionarily conserved component of DNA replication machinery in eukaryotes, in installing the imprint through a non-canonical primase activity and interaction with DNA Polα and Swi1. The high degree of conservation of DNA replication machinery, especially the presence of the T7 gene 4 helicase/primase domain in the mammalian orthologs of Mcm10 suggests that similar mechanisms of DNA imprinting may play a role during cell differentiation in metazoans.
本文详细阐述了一项新研究报告的发现,该报告可能阐明了新型 DNA 印迹的生化本质,以及其在有丝分裂酵母细胞分化过程中形成的机制。有丝分裂酵母(裂殖酵母)的交配型转换过程表现出典型的哺乳动物干细胞谱系的特征,其中细胞每两次分裂就会产生一个相同的细胞和一个分化的细胞。这种发育不对称性被认为在滞后链合成过程中在 mat1 基因座产生 DNA 链特异性印迹,并通过不对称、半保守性 DNA 复制过程将其分配到两个子细胞之一中,从而发挥作用。这种印迹的性质及其产生机制一直是研究和争论的主题。Singh 等人的最近一份报告(Nucleic Acids Res 47:3422-3433. https://doi.org/10.1093/nar/gkz092, 2019)提供了令人信服的证据,支持在 mat1 DNA 中,印迹部分是一个核苷酸,并且证明了 Mcm10/Cdc23(真核生物 DNA 复制机制中重要的进化保守成分)的作用,它通过非经典的引物酶活性以及与 DNA Polα 和 Swi1 的相互作用,安装印迹。DNA 复制机制的高度保守性,特别是在哺乳动物 Mcm10 同源物中存在 T7 基因 4 解旋酶/引物酶结构域,表明类似的 DNA 印迹机制可能在后生动物的细胞分化过程中发挥作用。