Meta-regulation: microRNA regulation of glucose and lipid metabolism

被引:152
作者
Lynn, Francis C. [1 ,2 ]
机构
[1] Univ British Columbia, Dept Surg, Child & Family Res Inst, Vancouver, BC V5Z 4H4, Canada
[2] Univ British Columbia, Dept Cellular & Physiol Sci, Child & Family Res Inst, Vancouver, BC V5Z 4H4, Canada
关键词
HETEROCHRONIC GENE LIN-14; PANCREATIC BETA-CELLS; CAENORHABDITIS-ELEGANS; C-ELEGANS; IN-VIVO; POSTTRANSCRIPTIONAL REGULATION; DEVELOPMENTAL SWITCH; INSULIN-RESISTANCE; EXPRESSION; RNA;
D O I
10.1016/j.tem.2009.05.007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Maintenance of homeostalsis during environmental flux requires constant metabolic adjustment, achieved partly through the fine regulation of gene expression. MicroRNAs are key players in this regulatory milieu; they have been implicated in regulating gene expression within several metabolically active tissues including the endocrine pancreas, liver and adipose tissue. Recent studies, for example, implicate miR-375 in pancreatic islet cell viability and function, and removal or overexpression of miR-375 profoundly affects glucose metabolism. In the liver, miR-122 is important for normal lipid metabolism. In fact, misexpression of miRNAs can occur in some diseases, suggesting that restoring miRNA expression is a potential therapeutic approach for both metabolic syndrome and diabetes.
引用
收藏
页码:452 / 459
页数:8
相关论文
共 72 条
  • [1] A HIERARCHY OF REGULATORY GENES CONTROLS A LARVA-TO-ADULT DEVELOPMENTAL SWITCH IN C-ELEGANS
    AMBROS, V
    [J]. CELL, 1989, 57 (01) : 49 - 57
  • [2] HETEROCHRONIC MUTANTS OF THE NEMATODE CAENORHABDITIS-ELEGANS
    AMBROS, V
    HORVITZ, HR
    [J]. SCIENCE, 1984, 226 (4673) : 409 - 416
  • [3] THE LIN-14 LOCUS OF CAENORHABDITIS-ELEGANS CONTROLS THE TIME OF EXPRESSION OF SPECIFIC POSTEMBRYONIC DEVELOPMENTAL EVENTS
    AMBROS, V
    HORVITZ, HR
    [J]. GENES & DEVELOPMENT, 1987, 1 (04) : 398 - 414
  • [4] MicroRNA-124a regulates Foxa2 expression and intracellular signaling in pancreatic β-cell lines
    Baroukh, Nadine
    Ravier, Magalie A.
    Loder, Merewyn K.
    Hill, Elaine V.
    Bounacer, Ali
    Scharfmann, Raphael
    Rutter, Guy A.
    Van Obberghen, Emmanuel
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (27) : 19575 - 19588
  • [5] MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004)
    Bartel, David P.
    [J]. CELL, 2007, 131 (04) : 11 - 29
  • [6] Adipose tissue selective insulin receptor knockout protects against obesity and obesity-related glucose intolerance
    Blüher, M
    Michael, MD
    Peroni, OD
    Ueki, K
    Carter, N
    Kahn, BB
    Kahn, CR
    [J]. DEVELOPMENTAL CELL, 2002, 3 (01) : 25 - 38
  • [7] RNA-Based Therapeutics: Ready for Delivery?
    Bonetta, Laura
    [J]. CELL, 2009, 136 (04) : 581 - 584
  • [8] Quantitative differential expression analysis reveals miR-7 as major islet microRNA
    Bravo-Egana, Valia
    Rosero, Samuel
    Molano, R. Damaris
    Pileggi, Antonello
    Ricordi, Camillo
    Dominguez-Bendala, Juan
    Pastori, Ricardo L.
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2008, 366 (04) : 922 - 926
  • [9] A muscle-specific insulin receptor knockout exhibits features of the metabolic syndrome of NIDDM without altering glucose tolerance
    Bruning, JC
    Michael, MD
    Winnay, JN
    Hayashi, T
    Horsch, D
    Accili, D
    Goodyear, LJ
    Kahn, CR
    [J]. MOLECULAR CELL, 1998, 2 (05) : 559 - 569
  • [10] Origins and Mechanisms of miRNAs and siRNAs
    Carthew, Richard W.
    Sontheimer, Erik J.
    [J]. CELL, 2009, 136 (04) : 642 - 655