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线粒体基因组消除的自然和人工机制

Natural and Artificial Mechanisms of Mitochondrial Genome Elimination.

作者信息

Zakirova Elvira G, Muzyka Vladimir V, Mazunin Ilya O, Orishchenko Konstantin E

机构信息

Federal Research Center Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, Russia.

Department of Genetic Technologies, Novosibirsk State University, 630090 Novosibirsk, Russia.

出版信息

Life (Basel). 2021 Jan 20;11(2):76. doi: 10.3390/life11020076.

DOI:10.3390/life11020076
PMID:33498399
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7909434/
Abstract

The generally accepted theory of the genetic drift of mitochondrial alleles during mammalian ontogenesis is based on the presence of a selective bottleneck in the female germline. However, there is a variety of different theories on the pathways of genetic regulation of mitochondrial DNA (mtDNA) dynamics in oogenesis and adult somatic cells. The current review summarizes present knowledge on the natural mechanisms of mitochondrial genome elimination during mammalian development. We also discuss the variety of existing and developing methodologies for artificial manipulation of the mtDNA heteroplasmy level. Understanding of the basics of mtDNA dynamics will shed the light on the pathogenesis and potential therapies of human diseases associated with mitochondrial dysfunction.

摘要

关于哺乳动物个体发育过程中线粒体等位基因遗传漂变的普遍接受的理论是基于雌性生殖系中存在选择性瓶颈。然而,关于卵子发生和成年体细胞中线粒体DNA(mtDNA)动态遗传调控途径存在多种不同理论。本综述总结了目前关于哺乳动物发育过程中线粒体基因组消除自然机制的知识。我们还讨论了用于人工操纵mtDNA异质性水平的各种现有和正在开发的方法。对mtDNA动态基础的理解将为与线粒体功能障碍相关的人类疾病的发病机制和潜在治疗方法提供线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a70e/7909434/b5974048dbe8/life-11-00076-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a70e/7909434/b5974048dbe8/life-11-00076-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a70e/7909434/b5974048dbe8/life-11-00076-g001.jpg

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本文引用的文献

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Cell identity and nucleo-mitochondrial genetic context modulate OXPHOS performance and determine somatic heteroplasmy dynamics.细胞身份和核线粒体遗传背景调节氧化磷酸化性能并决定体细胞异质性动态。
Sci Adv. 2020 Jul 29;6(31):eaba5345. doi: 10.1126/sciadv.aba5345. eCollection 2020 Jul.
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A bacterial cytidine deaminase toxin enables CRISPR-free mitochondrial base editing.一种细菌胞嘧啶脱氨酶毒素可实现无 CRISPR 的线粒体碱基编辑。
Nature. 2020 Jul;583(7817):631-637. doi: 10.1038/s41586-020-2477-4. Epub 2020 Jul 8.
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Life (Basel). 2021 Sep 21;11(9):991. doi: 10.3390/life11090991.
线粒体疾病:未来的希望。
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Manipulation of mitochondrial genes and mtDNA heteroplasmy.线粒体基因与线粒体DNA异质性的操控
Methods Cell Biol. 2020;155:441-487. doi: 10.1016/bs.mcb.2019.12.004. Epub 2020 Jan 20.
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EMBO Rep. 2020 Mar 4;21(3):e49612. doi: 10.15252/embr.201949612. Epub 2020 Feb 19.
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Mitochondrion: I am more than a fuel server.线粒体:我不只是一个供能者。
Ann Transl Med. 2019 Oct;7(20):594. doi: 10.21037/atm.2019.08.22.
8
Sorting mtDNA Species-the Role of nDNA-mtDNA Co-evolution.分拣 mtDNA 物种——nDNA-mtDNA 共同进化的作用。
Cell Metab. 2019 Dec 3;30(6):1002-1004. doi: 10.1016/j.cmet.2019.11.005.
9
Reversion after replacement of mitochondrial DNA.线粒体DNA替换后的回复突变
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10
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