Dual role of the carboxyl-terminal region of pig liver l-kynurenine 3-monooxygenase: mitochondrial-targeting signal and enzymatic activity*

作者：Hirai Kumiko^*; Kuroyanagi Hidehito; Tatebayashi Yoshitaka; Hayashi Yoshitaka; Hirabayashi Takahashi Kanako; Saito Kuniaki; Haga Seiich; Uemura Tomihiko; Izumi Susumu

来源：Journal of Biochemistry, 2010, 148(6): 639-650.

DOI：10.1093/jb/mvq099

• Carboxyl-terminal truncation
• hydrophobic C-terminal domain
• l-kynurenine 3-monooxygenase
• mitochondrial targeting signal
• mitochondrial tail-anchored protein

l-kynurenine 3-monooxygenase (KMO) is an NAD(P)H-dependent flavin monooxygenase that catalyses the hydroxylation of l-kynurenine to 3-hydroxykynurenine, and is localized as an oligomer in the mitochondrial outer membrane. In the human brain, KMO may play an important role in the formation of two neurotoxins, 3-hydroxykynurenine and quinolinic acid, both of which provoke severe neurodegenerative diseases. In mosquitos, it plays a role in the formation both of eye pigment and of an exflagellation-inducing factor (xanthurenic acid). Here, we present evidence that the C-terminal region of pig liver KMO plays a dual role. First, it is required for the enzymatic activity. Second, it functions as a mitochondrial targeting signal as seen in monoamine oxidase B (MAO B) or outer membrane cytochrome b(5). The first role was shown by the comparison of the enzymatic activity of two mutants (C-terminally FLAG-tagged KMO and carboxyl-terminal truncation form, KMO delta C50) with that of the wild-type enzyme expressed in COS-7 cells. The second role was demonstrated with fluorescence microscopy by the comparison of the intracellular localization of the wild-type, three carboxyl-terminal truncated forms (delta C20, delta C30 and delta C50), C-terminally FLAG-tagged wild-type and a mutant KMO, where two arginine residues, Arg461-Arg462, were replaced with Ser residues.

• 出版日期2010-12