Cell death promoted by homologous DNA interaction from bacteria to humans.

Advances in Biophysics Pub Date : 2004-01-01
Kohji Kusano
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引用次数: 0

Abstract

Pairing between homologous DNA controls cellular functions including double-strand break repair, mitotic recombination, and progression of DNA replication forks, as well as chiasma formation during meiosis. Here I summarize that homologous interaction could promote the cell killing in bacteria, yeast, and multicellular organisms. The mechanisms of cell killing are categorized into two types: (1) the killing due to the accumulation of extrachromosomal DNA; (2) the killing induced by Holliday junction structures. I propose that the mechanisms of such killing function as novel apoptotic pathways in the cells carrying severe DNA damages to eliminate such damages from cell population.

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从细菌到人的同源DNA相互作用促进细胞死亡。
同源DNA之间的配对控制着细胞功能,包括双链断裂修复、有丝分裂重组和DNA复制叉的进展,以及减数分裂期间交叉的形成。本文总结了同源相互作用在细菌、酵母和多细胞生物中促进细胞杀伤的研究进展。细胞杀伤机制可分为两种类型:(1)染色体外DNA的累积杀伤;(2) Holliday结结构引起的杀伤。我提出这种杀伤功能的机制是在携带严重DNA损伤的细胞中出现新的凋亡途径,以消除细胞群中的这种损伤。
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Preface Illegitimate recombination mediated by double-strand break and end-joining in Escherichia coli. Genetic and physiological regulation of non-homologous end-joining in mammalian cells. The function of RecQ helicase gene family (especially BLM) in DNA recombination and joining. Nijmegen breakage syndrome and DNA double strand break repair by NBS1 complex.
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