| Literature DB >> 27667668 |
Ling Yang1, Ping Li1, Wenjing Yang2, Xiangbo Ruan1, Kurtis Kiesewetter1, Jun Zhu2, Haiming Cao3.
Abstract
To systemically identify long noncoding RNAs (lncRNAs) regulating energy metabolism, we performed transcriptome analyses to simultaneously profile mRNAs and lncRNAs in key metabolic organs in mice under pathophysiologically representative metabolic conditions. Of 4,759 regulated lncRNAs, function-oriented filters yield 359 tissue-specifically regulated and metabolically sensitive lncRNAs that are predicted by lncRNA-mRNA correlation analyses to function in diverse aspects of energy metabolism. Specific regulations of liver metabolically sensitive lncRNAs (lncLMS) by nutrients, metabolic hormones, and key transcription factors were further defined in primary hepatocytes. Combining genome-wide screens, bioinformatics function predictions, and cell-based analyses, we developed an integrative roadmap to identify lncRNA metabolic regulators. An lncLMS was experimentally confirmed in mice to suppress lipogenesis by forming a negative feedback loop in the SREBP1c pathway. Taken together, this study supports that a class of lncRNAs function as important metabolic regulators and establishes a framework for systemically investigating the role of lncRNAs in physiological homeostasis. Published by Elsevier Inc.Entities:
Keywords: diabetes; energy metabolism; glucose; insulin; lincRNA; lipid; lncRNA; long non-coding RNA; metabolic disease; obesity
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Year: 2016 PMID: 27667668 PMCID: PMC5181118 DOI: 10.1016/j.cmet.2016.08.019
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287