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参与程序性双链断裂DNA修复的草履虫PolX DNA聚合酶的保真度、特异性及进化

Fidelity, specialization, and evolution of Paramecium PolX DNA polymerases involved in programmed double-strand break DNA repair.

作者信息

Antonin Nourisson, Sophia Missoury, Soizick Lucas-Staat, Ahmed Haouz, Marc Delarue

机构信息

Unit of Architecture and Dynamics of Biological Macromolecules, Université Paris Ci té, CNRS UMR 3528, 25-28 rue du Docteur Roux, Institut Pasteur, 75015 Paris, France.

Sorbonne Université, Collège Doctoral, ED 515, 75005 Paris, France.

出版信息

Nucleic Acids Res. 2025 Aug 11;53(15). doi: 10.1093/nar/gkaf786.

Abstract

Repairing programmed DNA double-strand breaks (DSBs) is crucial in the lifecycle of Paramecium tetraurelia, especially during its sexual reproduction phase when its somatic polyploid macronucleus is lost. The formation of a new macronucleus involves programmed genome rearrangements, introducing DNA DSBs at ∼45 000 loci. Paramecium tetraurelia employs a non-homologous end joining (NHEJ) mechanism for the faithful repair of these DSBs. There are four genes encoding DNA polymerases of family X in the genome, one of which was found recently to colocalize with other NHEJ proteins in the nucleus. Here we have characterized all four enzymes and shown that they are generally very faithful. They fall into two functional classes that may specialize in the distinct repair contexts encountered during DSB DNA repair. Biochemical assays, site-directed mutagenesis, and X-ray structures of mutants of human Polλ incorporating sequence determinants from P. tetraurelia PolX or metazoan Polβ are used to investigate the origin of their fidelity. Our findings suggest that Paramecium PolX enzymes may represent evolutionary intermediates between metazoan Polβ and Polλ. A general classification of DNA PolXs based on clustering methods indicates that our results can be generalized to plant DNA PolXs (Polλ-like) involved in DSB DNA repair generated by CRISPR-Cas9 engineering.

摘要

修复程序性DNA双链断裂(DSB)在四膜虫的生命周期中至关重要,尤其是在其有性生殖阶段,此时其体细胞多倍体大核会丢失。新大核的形成涉及程序性基因组重排,在约45000个位点引入DNA DSB。四膜虫采用非同源末端连接(NHEJ)机制来准确修复这些DSB。基因组中有四个编码X家族DNA聚合酶的基因,其中一个最近被发现与其他NHEJ蛋白在细胞核中共定位。在这里,我们对所有四种酶进行了表征,并表明它们通常非常准确。它们分为两个功能类别,可能专门负责DSB DNA修复过程中遇到的不同修复情况。利用结合了四膜虫PolX或后生动物Polβ序列决定因素的人Polλ突变体的生化分析、定点诱变和X射线结构来研究其准确性的来源。我们的研究结果表明,四膜虫PolX酶可能代表后生动物Polβ和Polλ之间的进化中间体。基于聚类方法对DNA PolXs进行的一般分类表明,我们的结果可以推广到参与CRISPR-Cas9工程产生的DSB DNA修复的植物DNA PolXs(Polλ样)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d014/12362244/70e1af013eda/gkaf786figgra1.jpg

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