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Vitamin K 2 Is a Mitochondrial Electron Carrier That Rescues Pink1 Deficiency
Author(s) -
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
Publication year - 2012
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.1218632
Subject(s) - pink1 , mitochondrion , adenosine triphosphate , gene , microbiology and biotechnology , mitochondrial dna , biology , electron transport chain , chemistry , mitophagy , biochemistry , autophagy , apoptosis
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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