A Long Noncoding RNA Transcriptional Regulatory Circuit Drives Thermogenic Adipocyte Differentiation

被引:237
作者
Zhao, Xu-Yun [1 ,2 ]
Li, Siming [1 ,2 ]
Wang, Guo-Xiao [1 ,2 ]
Yu, Qi [1 ,2 ]
Lin, Jiandie D. [1 ,2 ]
机构
[1] Univ Michigan, Med Ctr, Inst Life Sci, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Med Ctr, Dept Cell & Dev Biol, Ann Arbor, MI 48109 USA
关键词
BROWN ADIPOSE-TISSUE; ADULT HUMANS; ENERGY-EXPENDITURE; FAT DEVELOPMENT; WHITE FAT; IN-VIVO; PROTEIN; COLD; CELL; IDENTIFICATION;
D O I
10.1016/j.molcel.2014.06.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Brown and beige/brite fats generate heat via uncoupled respiration to defend against cold. The total mass and activity of thermogenic adipose tissues are also tightly linked to systemic energy and nutrient homeostasis. Despite originating from distinct progenitors, brown and beige adipocytes acquire remarkably similar molecular and metabolic characteristics during differentiation through the action of a network of transcription factors and cofactors. How this regulatory network interfaces with long noncoding RNAs (lncRNAs), an emerging class of developmental regulators, remains largely unexplored. Here, we globally profiled lncRNA gene expression during thermogenic adipocyte formation and identified Brown fat lncRNA 1 (Blnc1) as a nuclear lncRNA that promotes brown and beige adipocyte differentiation and function. Blnc1 forms a ribonucleoprotein complex with transcription factor EBF2 to stimulate the thermogenic gene program. Further, Blnc1 itself is a target of EBF2, thereby forming a feedforward regulatory loop to drive adipogenesis toward thermogenic phenotype.
引用
收藏
页码:372 / 382
页数:11
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