品脱1
线粒体
三磷酸腺苷
基因
细胞生物学
粒体自噬
生物
化学
电子传输链
线粒体DNA
生物化学
自噬
细胞凋亡
作者
Melissa Vos,Giovanni Esposito,Janaka N. Edirisinghe,Sven Vilain,Dominik Haddad,Jan R. Slabbaert,Stefanie Van Meensel,Onno Schaap,Bart De Strooper,R. Meganathan,Vanessa A. Morais,Patrik Verstreken
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2012-05-11
卷期号:336 (6086): 1306-1310
被引量:350
标识
DOI:10.1126/science.1218632
摘要
Human UBIAD1 localizes to mitochondria and converts vitamin K(1) to vitamin K(2). Vitamin K(2) is best known as a cofactor in blood coagulation, but in bacteria it is a membrane-bound electron carrier. Whether vitamin K(2) exerts a similar carrier function in eukaryotic cells is unknown. We identified Drosophila UBIAD1/Heix as a modifier of pink1, a gene mutated in Parkinson's disease that affects mitochondrial function. We found that vitamin K(2) was necessary and sufficient to transfer electrons in Drosophila mitochondria. Heix mutants showed severe mitochondrial defects that were rescued by vitamin K(2), and, similar to ubiquinone, vitamin K(2) transferred electrons in Drosophila mitochondria, resulting in more efficient adenosine triphosphate (ATP) production. Thus, mitochondrial dysfunction was rescued by vitamin K(2) that serves as a mitochondrial electron carrier, helping to maintain normal ATP production.
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