| Literature DB >> 28812581 |
Yuta Hiraike1, Hironori Waki1,2, Jing Yu1, Masahiro Nakamura1, Kana Miyake1, Gaku Nagano3, Ryo Nakaki4, Ken Suzuki1, Hirofumi Kobayashi1, Shogo Yamamoto4, Wei Sun1, Tomohisa Aoyama1, Yusuke Hirota1, Haruya Ohno3, Kenji Oki3, Masayasu Yoneda3, Andrew P White5, Yu-Hua Tseng6, Aaron M Cypess7, Therese J Larsen8,9, Naja Z Jespersen8,10, Camilla Scheele8,11, Shuichi Tsutsumi4, Hiroyuki Aburatani4, Toshimasa Yamauchi1, Takashi Kadowaki1.
Abstract
Brown fat dissipates energy as heat and protects against obesity. Here, we identified nuclear factor I-A (NFIA) as a transcriptional regulator of brown fat by a genome-wide open chromatin analysis of murine brown and white fat followed by motif analysis of brown-fat-specific open chromatin regions. NFIA and the master transcriptional regulator of adipogenesis, PPARγ, co-localize at the brown-fat-specific enhancers. Moreover, the binding of NFIA precedes and facilitates the binding of PPARγ, leading to increased chromatin accessibility and active transcription. Introduction of NFIA into myoblasts results in brown adipocyte differentiation. Conversely, the brown fat of NFIA-knockout mice displays impaired expression of the brown-fat-specific genes and reciprocal elevation of muscle genes. Finally, expression of NFIA and the brown-fat-specific genes is positively correlated in human brown fat. These results indicate that NFIA activates the cell-type-specific enhancers and facilitates the binding of PPARγ to control the brown fat gene program.Entities:
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Year: 2017 PMID: 28812581 PMCID: PMC5885759 DOI: 10.1038/ncb3590
Source DB: PubMed Journal: Nat Cell Biol ISSN: 1465-7392 Impact factor: 28.213