| Literature DB >> 34506728 |
Aileen Mendoza1, Yasushi Takemoto1, Kevin Tan Cruzado1, Shadi Sedghi Masoud2, Akiko Nagata2, Ajcharapan Tantipanjaporn3, Satoshi Okuda3, Fumihiro Kawagoe4, Ryota Sakamoto2, Minami Odagi2, Sayuri Mototani4, Moeka Togashi5, Makoto Kawatani6, Harumi Aono6, Hiroyuki Osada6, Hayato Nakagawa7, Tatsuya Higashi5, Atsushi Kittaka4, Kazuo Nagasawa8, Motonari Uesugi9.
Abstract
Lactone-vitamin D3 is a major metabolite of vitamin D3, a lipophilic vitamin biosynthesized in numerous life forms by sunlight exposure. Although lactone-vitamin D3 was discovered 40 years ago, its biological role remains largely unknown. Chemical biological analysis of its photoaffinity probe identified the hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha (HADHA), a mitochondrial enzyme that catalyzes β-oxidation of long-chain fatty acids, as its selective binding protein. Intriguingly, the interaction of lactone-vitamin D3 with HADHA does not affect the HADHA enzymatic activity but instead limits biosynthesis of carnitine, an endogenous metabolite required for the transport of fatty acids into the mitochondria for β-oxidation. Lactone-vitamin D3 dissociates the protein-protein interaction of HADHA with trimethyllysine dioxygenase (TMLD), thereby impairing the TMLD enzyme activity essential in carnitine biosynthesis. These findings suggest a heretofore undescribed role of lactone-vitamin D3 in lipid β-oxidation and carnitine biosynthesis, and possibly in sunlight-dependent shifts of lipid metabolism in animals.Entities:
Keywords: CYP24A1; HADHA; TMLD; TMLHE; carnitine; lactone-vitamin D3; lipid metabolism; metabolic shift; vitamin D; β-oxidation
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Year: 2021 PMID: 34506728 DOI: 10.1016/j.chembiol.2021.08.008
Source DB: PubMed Journal: Cell Chem Biol ISSN: 2451-9448 Impact factor: 9.039