Why do mammalian mitochondria possess a mismatch repair activity?

被引:21
作者
Mason, PA [1 ]
Lightowlers, RN [1 ]
机构
[1] Newcastle Univ, Sch Neurol Neurobiol & Psychiat, Sch Med, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
来源
FEBS LETTERS | 2003年 / 554卷 / 1-2期
基金
英国惠康基金;
关键词
mitochondrial DNA; MtDNA repair; mitochondrial mismatch repair;
D O I
10.1016/S0014-5793(03)01169-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
All nucleated mammalian cells contain mitochondrial DNA, a small (approximately 15-17 kb) circular genome found in the matrix. This molecule is present in multiple copies, with numbers routinely exceeding 1000 per cell. Many pathogenic mutations of this genome have been reported, with the vast majority being highly recessive. A mismatch repair activity has been recently described in mitochondria that shows no strand bias for correcting point mutations. What could be the physiological function of such an activity? Mammalian mtDNA is remarkable in being a patchwork of many short repeat sequences. With reference to several recent publications, we hypothesise that the function of this activity is to preserve the mitochondrial genome by repairing short loop out sequences that would otherwise be lost as mitochondrial DNA polymerase gamma replicates the mitochondrial genome. (C) 2003 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:6 / 9
页数:4
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