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KSRP ablation enhances brown fat gene program in white adipose tissue through reduced miR-150 expression.
Chou, Chu-Fang; Lin, Yi-Yu; Wang, Hsu-Kun; Zhu, Xiaolin; Giovarelli, Matteo; Briata, Paola; Gherzi, Roberto; Garvey, W Timothy; Chen, Ching-Yi.
Affiliation
  • Chou CF; Department of Biochemistry and Molecular Genetics, University of Alabama at Birmingham, Birmingham, AL.
  • Lin YY; Department of Biochemistry and Molecular Genetics, University of Alabama at Birmingham, Birmingham, AL.
  • Wang HK; Department of Biochemistry and Molecular Genetics, University of Alabama at Birmingham, Birmingham, AL.
  • Zhu X; Department of Nutrition Sciences, University of Alabama at Birmingham, Birmingham, AL.
  • Giovarelli M; Gene Expression Regulation Laboratory, Istituto Nazionale per la Ricerca sul Cancro, Genova, Italy.
  • Briata P; Gene Expression Regulation Laboratory, Istituto Nazionale per la Ricerca sul Cancro, Genova, Italy.
  • Gherzi R; Gene Expression Regulation Laboratory, Istituto Nazionale per la Ricerca sul Cancro, Genova, Italy.
  • Garvey WT; Department of Nutrition Sciences, University of Alabama at Birmingham, Birmingham, AL garveyt@uab.edu cchen@uab.edu.
  • Chen CY; Department of Biochemistry and Molecular Genetics, University of Alabama at Birmingham, Birmingham, AL garveyt@uab.edu cchen@uab.edu.
Diabetes ; 63(9): 2949-61, 2014 Sep.
Article in En | MEDLINE | ID: mdl-24722250
ABSTRACT
Brown adipose tissue oxidizes chemical energy for heat generation and energy expenditure. Promoting brown-like transformation in white adipose tissue (WAT) is a promising strategy for combating obesity. Here, we find that targeted deletion of KH-type splicing regulatory protein (KSRP), an RNA-binding protein that regulates gene expression at multiple levels, causes a reduction in body adiposity. The expression of brown fat-selective genes is increased in subcutaneous/inguinal WAT (iWAT) of Ksrp(-/-) mice because of the elevated expression of PR domain containing 16 and peroxisome proliferator-activated receptor gamma coactivator 1α, which are key regulators promoting the brown fat gene program. The expression of microRNA (miR)-150 in iWAT is decreased due to impaired primary miR-150 processing in the absence of KSRP. We show that miR-150 directly targets and represses Prdm16 and Ppargc1a, and that forced expression of miR-150 attenuates the elevated expression of brown fat genes caused by KSRP deletion. This study reveals the in vivo function of KSRP in controlling brown-like transformation of iWAT through post-transcriptional regulation of miR-150 expression.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Adipose Tissue, Brown / Trans-Activators / MicroRNAs / Adipose Tissue, White Limits: Animals Language: En Journal: Diabetes Year: 2014 Document type: Article Affiliation country: Albania

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Adipose Tissue, Brown / Trans-Activators / MicroRNAs / Adipose Tissue, White Limits: Animals Language: En Journal: Diabetes Year: 2014 Document type: Article Affiliation country: Albania