Author/Authors :
Vera Mugoni، نويسنده , , Ruben Postel، نويسنده , , Valeria Catanzaro، نويسنده , , Elisa De Luca، نويسنده , , Emilia Turco، نويسنده , , Giuseppe Digilio، نويسنده , , Lorenzo Silengo، نويسنده , , Michael P. Murphy، نويسنده , , Claudio Medana، نويسنده , , Didier Y.R. Stainier، نويسنده , , Jeroen Bakkers، نويسنده , , Massimo M. Santoro، نويسنده ,
Abstract :
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.