MacAlpine D M, Perlman P S, Butow R A
Department of Molecular Biology, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd, Dallas, TX 75390-9148, USA.
EMBO J. 2000 Feb 15;19(4):767-75. doi: 10.1093/emboj/19.4.767.
Mitochondrial DNA (mtDNA) is inherited as a protein-DNA complex (the nucleoid). We show that activation of the general amino acid response pathway in rho(+) and rho(-) petite cells results in an increased number of nucleoids without an increase in mtDNA copy number. In rho(-) cells, activation of the general amino acid response pathway results in increased intramolecular recombination between tandemly repeated sequences of rho(-) mtDNA to produce small, circular oligomers that are packaged into individual nucleoids, resulting in an approximately 10-fold increase in nucleoid number. The parsing of mtDNA into nucleoids due to general amino acid control requires Ilv5p, a mitochondrial protein that also functions in branched chain amino acid biosynthesis, and one or more factors required for mtDNA recombination. Two additional proteins known to function in mtDNA recombination, Abf2p and Mgt1p, are also required for parsing mtDNA into a larger number of nucleoids, although expression of these proteins is not under general amino acid control. Increased nucleoid number leads to increased mtDNA transmission, suggesting a mechanism to enhance mtDNA inheritance under amino acid starvation conditions.
线粒体DNA(mtDNA)作为一种蛋白质-DNA复合物(类核)进行遗传。我们发现,在ρ(+)和ρ(-)小菌落细胞中,通用氨基酸应答途径的激活会导致类核数量增加,而mtDNA拷贝数并未增加。在ρ(-)细胞中,通用氨基酸应答途径的激活会导致ρ(-)mtDNA串联重复序列之间的分子内重组增加,从而产生小的环状寡聚物,这些寡聚物被包装成单个类核,导致类核数量增加约10倍。由于通用氨基酸控制而将mtDNA解析为类核需要Ilv5p,一种在线粒体中也参与支链氨基酸生物合成的蛋白质,以及mtDNA重组所需的一种或多种因子。另外两种已知在mtDNA重组中起作用的蛋白质Abf2p和Mgt1p,也参与将mtDNA解析为更多类核的过程,尽管这些蛋白质的表达不受通用氨基酸控制。类核数量的增加导致mtDNA传递增加,这表明在氨基酸饥饿条件下存在一种增强mtDNA遗传的机制。