MITOCHONDRIAL DNA RECOMBINATION, REPAIR AND SEGREGATION, RECENT SCIENTIFIC DATA AND PERSPECTIVES

A. Dietrich
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引用次数: 2

Abstract

Dynamics, maintenance and transmission of the mitochondrial DNA (mtDNA) are at the forefront of organellar genetics. Recombination plays a major role in these processes in many organisms and has mostly been documented at the genetic and molecular level in yeast and plant mitochondria. In these organisms, repeat-mediated recombination generates subgenomes and alternative mtDNA configurations. On the other hand, recombination takes part in mtDNA repair pathways, including error-prone mechanisms like break-induced replication. In plants, minor alternative configurations can segregate from the heteroplasmic state and become predominant through substoichiometric shifting. Ectopic recombination and recombination-mediated repair are major contributors to the evolution and transmission of the plant mitochondrial genome. These mechanisms are supported by a series of nuclear-encoded and mitochondrially imported factors of prokaryotic origin. The situation differs in mammals, where mitochondria essentially lack such factors. Historically, the occurrence of recombination in mammalian mitochondria has been a matter of debate and has been considered to be rare. The most recent investigations brought evidence for mtDNA recombination intermediates and active homologous recombination in heart and brain mitochondria. The issue is of importance, as mutations in the mtDNA are the cause of multiple, severe and incurable neurodegenerative diseases. Mutations are usually heteroplasmic and the onset of clinical symptoms is determined by the ratio of wild-type to mutant mtDNA, with a typical threshold effect. Heteroplasmy yields mitotic segregation, i.e. the proportion of mutated mtDNA copies may shift in daughter cells. In post-mitotic tissues, mutated mtDNA copies are often preferentially amplified, leading to clonal expansion. Finally, mtDNA genotypes may segregate between generations. The mechanisms underlying all these fundamental processes are little understood in mammals. Knowledge gained in plants and introduction of plant factors into mammalian model systems might shed new light into the field.
线粒体DNA重组,修复和分离,最新的科学数据和观点
线粒体DNA (mtDNA)的动力学、维持和传递处于细胞器遗传学的前沿。重组在许多生物体的这些过程中起着重要作用,并且主要在酵母和植物线粒体的遗传和分子水平上被记录。在这些生物体中,重复介导的重组产生亚基因组和替代的mtDNA结构。另一方面,重组参与了mtDNA修复途径,包括断裂诱导复制等容易出错的机制。在植物中,次要的替代构型可以从异质状态中分离出来,并通过亚化学计量位移成为优势构型。异位重组和重组介导的修复是植物线粒体基因组进化和传播的主要因素。这些机制是由一系列核编码和线粒体输入的原核起源因子支持的。哺乳动物的情况有所不同,线粒体基本上缺乏这些因素。从历史上看,哺乳动物线粒体重组的发生一直是一个有争议的问题,并且被认为是罕见的。最近的研究表明,在心脏和大脑线粒体中存在mtDNA重组中间体和活性同源重组。这个问题很重要,因为mtDNA的突变是多种严重且无法治愈的神经退行性疾病的原因。突变通常是异质性的,临床症状的发作由野生型与突变型mtDNA的比例决定,具有典型的阈值效应。异质性产生有丝分裂分离,即在子细胞中突变的mtDNA拷贝的比例可能发生变化。在有丝分裂后的组织中,突变的mtDNA拷贝经常被优先扩增,导致克隆扩增。最后,mtDNA基因型可能在代之间分离。所有这些基本过程背后的机制在哺乳动物中知之甚少。在植物方面获得的知识和将植物因子引入哺乳动物模型系统可能会为这一领域带来新的曙光。
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