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MicroRNA-33 regulates sterol regulatory element-binding protein 1 expression in mice

MicroRNAs (miRs) are small non-protein-coding RNAs that bind to specific mRNAs and inhibit translation or promote mRNA degradation. Recent reports have indicated that miR-33, which is located within the intron of sterol regulatory element-binding protein (SREBP) 2, controls cholesterol homoeostasis...

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Detalles Bibliográficos
Autores principales: Horie, Takahiro, Nishino, Tomohiro, Baba, Osamu, Kuwabara, Yasuhide, Nakao, Tetsushi, Nishiga, Masataka, Usami, Shunsuke, Izuhara, Masayasu, Sowa, Naoya, Yahagi, Naoya, Shimano, Hitoshi, Matsumura, Shigenobu, Inoue, Kazuo, Marusawa, Hiroyuki, Nakamura, Tomoyuki, Hasegawa, Koji, Kume, Noriaki, Yokode, Masayuki, Kita, Toru, Kimura, Takeshi, Ono, Koh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3863899/
https://www.ncbi.nlm.nih.gov/pubmed/24300912
http://dx.doi.org/10.1038/ncomms3883
Descripción
Sumario:MicroRNAs (miRs) are small non-protein-coding RNAs that bind to specific mRNAs and inhibit translation or promote mRNA degradation. Recent reports have indicated that miR-33, which is located within the intron of sterol regulatory element-binding protein (SREBP) 2, controls cholesterol homoeostasis and may be a potential therapeutic target for the treatment of atherosclerosis. Here we show that deletion of miR-33 results in marked worsening of high-fat diet-induced obesity and liver steatosis. Using miR-33(−/−)Srebf1(+/−) mice, we demonstrate that SREBP-1 is a target of miR-33 and that the mechanisms leading to obesity and liver steatosis in miR-33(−/−) mice involve enhanced expression of SREBP-1. These results elucidate a novel interaction between SREBP-1 and SREBP-2 mediated by miR-33 in vivo.