Ubiad1 Is an Antioxidant Enzyme that Regulates eNOS Activity by CoQ10 Synthesis

被引:169
作者
Mugoni, Vera [1 ]
Postel, Ruben [3 ,4 ,5 ]
Catanzaro, Valeria [1 ]
De Luca, Elisa [1 ]
Turco, Emilia [1 ]
Digilio, Giuseppe [1 ]
Silengo, Lorenzo [1 ]
Murphy, Michael P. [6 ]
Medana, Claudio [2 ]
Stainier, Didier Y. R. [7 ]
Bakkers, Jeroen [3 ,4 ,5 ]
Santoro, Massimo M. [1 ]
机构
[1] Univ Turin, Dept Mol Biotechnol & Hlth Sci, Ctr Mol Biotechnol, I-10126 Turin, Italy
[2] Univ Turin, Dept Chem, I-10126 Turin, Italy
[3] Hubrecht Inst KNAW, NL-3584 CT Utrecht, Netherlands
[4] Univ Med Ctr Utrecht, NL-3584 CT Utrecht, Netherlands
[5] Netherlands Heart Inst, NL-3584 CT Utrecht, Netherlands
[6] MRC, Mitochondrial Biol Unit, Cambridge CB2 0XY, England
[7] Max Planck Inst Heart & Lung Res, Dept Dev Genet, D-61231 Bad Nauheim, Germany
关键词
CRYSTALLINE CORNEAL-DYSTROPHY; NITRIC-OXIDE SYNTHASE; PROTEIN S-NITROSYLATION; COENZYME-Q; OXIDATIVE STRESS; CARDIOVASCULAR-SYSTEM; VASCULAR-DISEASE; BLOOD-FLOW; RAT-LIVER; IN-VIVO;
D O I
10.1016/j.cell.2013.01.013
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
Protection against oxidative damage caused by excessive reactive oxygen species (ROS) by an antioxidant network is essential for the health of tissues, especially in the cardiovascular system. Here, we identified a gene with important antioxidant features by analyzing a null allele of zebrafish ubiad1, called barolo (bar). bar mutants show specific cardiovascular failure due to oxidative stress and ROS-mediated cellular damage. Human UBIAD1 is a nonmitochondrial prenyltransferase that synthesizes CoQ10 in the Golgi membrane compartment. Loss of UBIAD1 reduces the cytosolic pool of the antioxidant CoQ10 and leads to ROS-mediated lipid peroxidation in vascular cells. Surprisingly, inhibition of eNOS prevents Ubiad1-dependent cardiovascular oxidative damage, suggesting a crucial role for this enzyme and nonmitochondrial CoQ10 in NO signaling. These findings identify UBIAD1 as a nonmitochondrial CoQ10-forming enzyme with specific cardiovascular protective function via the modulation of eNOS activity.
引用
收藏
页码:504 / 518
页数:15
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