Ad4BP/SF-1 regulates cholesterol synthesis to boost the production of steroids
- Authors
- Baba, Takashi; Otake, Hiroyuki; Inoue, Miki; Sato, Tetsuya; Ishihara, Yasuhiro; Moon, Ju-Yeon; Tsuchiya, Megumi; Miyabayashi, Kanako; Ogawa, Hidesato; Shima, Yuichi; Wang, Lixiang; Sato, Ryuichiro; Yamazaki, Takeshi; Suyama, Mikita; Nomura, Masatoshi; Choi, Man Ho; Ohkawa, Yasuyuki; Morohashi, Ken-ichirou
- Issue Date
- 2018-04
- Publisher
- Nature Publishing Group
- Citation
- Communications Biology, v.1, no.1
- Abstract
- Housekeeping metabolic pathways such as glycolysis are active in all cell types. In addition, many types of cells are equipped with cell-specific metabolic pathways. To properly perform their functions, housekeeping and cell-specific metabolic pathways must function cooperatively. However, the regulatory mechanisms that couple metabolic pathways remain largely unknown. Recently, we showed that the steroidogenic cell-specific nuclear receptor Ad4BP/SF-1, which regulates steroidogenic genes, also regulates housekeeping glycolytic genes. Here, we identify cholesterogenic genes as the targets of Ad4BP/SF-1. Further, we reveal that Ad4BP/SF-1 regulates Hummr, a candidate mediator of cholesterol transport from endoplasmic reticula to mitochondria. Given that cholesterol is the starting material for steroidogenesis and is synthesized from acetyl-CoA, which partly originates from glucose, our results suggest that multiple biological processes involved in synthesizing steroid hormones are governed by Ad4BP/SF-1. To our knowledge, this study provides the first example where housekeeping and cell-specific metabolism are coordinated at the transcriptional level.
- Keywords
- HIGH-DENSITY-LIPOPROTEIN; ATP-CITRATE-LYASE; PROTEIN/STEROIDOGENIC FACTOR-1; TRANSCRIPTIONAL REGULATION; PROTEIN; CELLS; GENE; STEROIDOGENESIS; METABOLISM; PROMOTERS; Ad4BP/SF-1; cholesterol; steroidogenesis
- ISSN
- 2399-3642
- URI
- https://pubs.kist.re.kr/handle/201004/121535
- DOI
- 10.1038/s42003-018-0020-z
- Appears in Collections:
- KIST Article > 2018
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