Literature DB >> 26321664

Identification of human ELOVL5 enhancer regions controlled by SREBP.

Akito Shikama1, Haruna Shinozaki2, Yoshinori Takeuchi1, Takashi Matsuzaka2, Yuichi Aita1, Tomoki Murayama1, Yoshikazu Sawada1, Xiaoying Piao1, Naoki Toya1, Yukari Oya1, Ayako Takarada1, Yukari Masuda1, Makiko Nishi1, Midori Kubota1, Yoshihiko Izumida1, Yoshimi Nakagawa2, Hitoshi Iwasaki2, Kazuto Kobayashi2, Shigeru Yatoh2, Hiroaki Suzuki2, Hiroaki Yagyu2, Yasushi Kawakami2, Nobuhiro Yamada2, Hitoshi Shimano2, Naoya Yahagi3.   

Abstract

Fatty acid elongase 5 (ELOVL5) is an enzyme involved in the synthesis of polyunsaturated fatty acids. Sterol Regulatory Element-binding Protein (SREBP)-1 activates ELOVL5 and increases polyunsaturated fatty acid synthesis, which in turn negatively affects SREBP-1 expression. Thus, ELOVL5 has been established as an SREBP-1 target gene and an important component of the negative feedback loop of de novo lipogenesis. However, the human ELOVL5 promoter/enhancer has not been fully analyzed and the location of SREBP biding sites around the ELOVL5 gene has yet to be defined. Here we performed a detailed promoter/enhancer analysis of human ELOVL5 gene, and identified two new SREBP binding sites, one in the 10 kb upstream region and one in the exon 1. These two SRE motifs are conserved among mammals and the mechanism found in the present study by which SREBP activates ELOVL5 is considered to be common in mammals. Through these findings, we clarified the molecular mechanism how SREBP activates ELOVL5, an important regulator of de novo lipogenesis.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Fatty acid synthesis; Polyunsaturated fatty acids; Transcription

Mesh:

Substances:

Year:  2015        PMID: 26321664     DOI: 10.1016/j.bbrc.2015.08.101

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  6 in total

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Journal:  Genome Biol       Date:  2017-03-28       Impact factor: 13.583

5.  Hepatic gene body hypermethylation is a shared epigenetic signature of murine longevity.

Authors:  Oliver Hahn; Thomas M Stubbs; Wolf Reik; Sebastian Grönke; Andreas Beyer; Linda Partridge
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6.  Bromide alleviates fatty acid-induced lipid accumulation in mouse primary hepatocytes through the activation of PPARα signals.

Authors:  Yujie Shi; Wenxiang Zhang; Yinlong Cheng; Chang Liu; Siyu Chen
Journal:  J Cell Mol Med       Date:  2019-04-29       Impact factor: 5.310

  6 in total

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