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NFIA与PPARγ共定位,并在转录水平上调控棕色脂肪基因程序。

NFIA co-localizes with PPARγ and transcriptionally controls the brown fat gene program.

作者信息

Hiraike Yuta, Waki Hironori, Yu Jing, Nakamura Masahiro, Miyake Kana, Nagano Gaku, Nakaki Ryo, Suzuki Ken, Kobayashi Hirofumi, Yamamoto Shogo, Sun Wei, Aoyama Tomohisa, Hirota Yusuke, Ohno Haruya, Oki Kenji, Yoneda Masayasu, White Andrew P, Tseng Yu-Hua, Cypess Aaron M, Larsen Therese J, Jespersen Naja Z, Scheele Camilla, Tsutsumi Shuichi, Aburatani Hiroyuki, Yamauchi Toshimasa, Kadowaki Takashi

机构信息

Department of Diabetes and Metabolic Diseases, Graduate School of Medicine, The University of Tokyo, Tokyo 113-8655, Japan.

Department of Molecular Science on Diabetes, Graduate School of Medicine, The University of Tokyo, Tokyo 113-8655, Japan.

出版信息

Nat Cell Biol. 2017 Sep;19(9):1081-1092. doi: 10.1038/ncb3590. Epub 2017 Aug 14.

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.

摘要

棕色脂肪以热量形式消耗能量,预防肥胖。在此,我们通过对小鼠棕色和白色脂肪进行全基因组开放染色质分析,随后对棕色脂肪特异性开放染色质区域进行基序分析,鉴定出核因子I-A(NFIA)为棕色脂肪的转录调节因子。NFIA与脂肪生成的主要转录调节因子PPARγ共同定位于棕色脂肪特异性增强子。此外,NFIA的结合先于并促进PPARγ的结合,导致染色质可及性增加和活跃转录。将NFIA导入成肌细胞可导致棕色脂肪细胞分化。相反,NFIA基因敲除小鼠的棕色脂肪显示棕色脂肪特异性基因表达受损,肌肉基因相互升高。最后,NFIA与棕色脂肪特异性基因的表达在人类棕色脂肪中呈正相关。这些结果表明,NFIA激活细胞类型特异性增强子,促进PPARγ的结合以控制棕色脂肪基因程序。

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