生物
线粒体融合
线粒体分裂
线粒体DNA
细胞生物学
线粒体
DNAJA3公司
线粒体内膜
线粒体凋亡诱导通道
内膜
内膜转移酶
遗传学
线粒体膜转运蛋白
基因
作者
Luis Carlos Tábara,Stephen P. Burr,Michele Frison,Suvagata Roy Chowdhury,Vincent Paupe,Yu Nie,Mark Johnson,Jara Villar-Azpillaga,Filipa Viegas,Mayuko Segawa,Hanish Anand,Kasparas Petkevicius,Patrick F. Chinnery,Julien Prudent
出处
期刊:Cell
[Elsevier]
日期:2024-06-07
卷期号:187 (14): 3619-3637.e27
被引量:3
标识
DOI:10.1016/j.cell.2024.05.017
摘要
Mitochondrial dynamics play a critical role in cell fate decisions and in controlling mtDNA levels and distribution. However, the molecular mechanisms linking mitochondrial membrane remodeling and quality control to mtDNA copy number (CN) regulation remain elusive. Here, we demonstrate that the inner mitochondrial membrane (IMM) protein mitochondrial fission process 1 (MTFP1) negatively regulates IMM fusion. Moreover, manipulation of mitochondrial fusion through the regulation of MTFP1 levels results in mtDNA CN modulation. Mechanistically, we found that MTFP1 inhibits mitochondrial fusion to isolate and exclude damaged IMM subdomains from the rest of the network. Subsequently, peripheral fission ensures their segregation into small MTFP1-enriched mitochondria (SMEM) that are targeted for degradation in an autophagic-dependent manner. Remarkably, MTFP1-dependent IMM quality control is essential for basal nucleoid recycling and therefore to maintain adequate mtDNA levels within the cell.
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