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KSRP Ablation Enhances Brown Fat Gene Program in White Adipose Tissue Through Reduced miR-150 Expression
Author(s) -
Chu-Fang Chou,
Yi-Yu Lin,
Hsu-Kun Wang,
Xiaolin Zhu,
Matteo Giovarelli,
Paola Briata,
Roberto Gherzi,
W. Timothy Garvey,
ChingYi Chen
Publication year - 2014
Publication title -
diabetes
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.219
H-Index - 330
eISSN - 1939-327X
pISSN - 0012-1797
DOI - 10.2337/db13-1901
Subject(s) - prdm16 , brown adipose tissue , white adipose tissue , adipose tissue , thermogenin , microrna , endocrinology , coactivator , fgf21 , medicine , gene expression , biology , rna splicing , thermogenesis , microbiology and biotechnology , gene , receptor , transcription factor , rna , fibroblast growth factor , genetics
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.

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