PPARα Is Regulated by miR-21 and miR-27b in Human Liver

被引:116
作者
Kida, Katsuhiko [1 ]
Nakajima, Miki [1 ]
Mohri, Takuya [1 ]
Oda, Yuki [1 ]
Takagi, Shingo [1 ]
Fukami, Tatsuki [1 ]
Yokoi, Tsuyoshi [1 ]
机构
[1] Kanazawa Univ, Fac Pharmaceut Sci, Kanazawa, Ishikawa 9201192, Japan
基金
日本学术振兴会;
关键词
lipid metabolism; microRNA; post-transcriptional regulation; PPAR alpha; PROLIFERATOR-ACTIVATED-RECEPTOR; PROTEIN-KINASE-C; EXPRESSION; MICRORNA; GENE; ACID; ENHANCER; CANCERS; BINDING; STRESS;
D O I
10.1007/s11095-011-0473-y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Peroxisome proliferator-activated receptor alpha (PPAR alpha) is an important transcriptional factor that regulates genes encoding endo/xenobiotic enzymes and lipid metabolizing enzymes. In this study, we investigated whether microRNAs (miRNAs) are involved in the regulation of PPAR alpha in human liver. Precursor or antisense oligonucleotide for miR-21 or miR-27b was transfected into HuH7 cells; expression of PPAR alpha and acyl-CoA synthetase M2B was determined by Western blot and real-time RT-PCR. Luciferase assay was performed to identify the functional miRNA recognition element (MRE). Expression levels of PPAR alpha, miR-21, and miR-27b in a panel of 24 human livers were determined. The overexpression and inhibition of miR-21 or miR-27b in HuH7 cells significantly decreased and increased the PPAR alpha protein level, respectively, but not PPAR alpha mRNA level. The miRNA-dependent regulation of PPAR alpha affected the expression of its downstream gene. Luciferase assay identified a functional MRE for miR-21 in the 3'-untranslated region of PPAR alpha. In human livers, the PPAR alpha protein levels were not correlated with PPAR alpha mRNA, but inversely correlated with the miR-21 levels, suggesting a substantial impact of miR-21, although the contribution of miR-27b could not be ruled out. We found that PPAR alpha in human liver is regulated by miRNAs.
引用
收藏
页码:2467 / 2476
页数:10
相关论文
共 32 条
[1]   Estrogen Receptor β1 Expression Is Regulated by miR-92 in Breast Cancer [J].
Al-Nakhle, Hakeemah ;
Burns, Philip A. ;
Cummings, Michele ;
Hanby, Andrew M. ;
Hughes, Thomas A. ;
Satheesha, Sampoorna ;
Shaaban, Abeer M. ;
Smith, Laura ;
Speirs, Valerie .
CANCER RESEARCH, 2010, 70 (11) :4778-4784
[2]   The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[3]   MicroRNA expression detected by oligonucleotide microarrays: System establishment and expression profiling in human tissues [J].
Barad, O ;
Meiri, E ;
Avniel, A ;
Aharonov, R ;
Barzilai, A ;
Bentwich, I ;
Einav, U ;
Glad, S ;
Hurban, P ;
Karov, Y ;
Lobenhofer, EK ;
Sharon, E ;
Shiboleth, YM ;
Shtutman, M ;
Bentwich, Z ;
Einat, P .
GENOME RESEARCH, 2004, 14 (12) :2486-2494
[4]   Peroxisome proliferator-activated receptor α induces hepatic expression of the human bile acid glucuronidating UDP-glucuronosyltransferase 2B4 enzyme [J].
Barbier, O ;
Duran-Sandoval, D ;
Pineda-Torra, I ;
Kosykh, V ;
Fruchart, JC ;
Staels, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (35) :32852-32860
[5]   The UDP-glucuronosyltransferase 1A9 enzyme is a peroxisome proliferator-activated receptor α and γ target gene [J].
Barbier, O ;
Villeneuve, L ;
Bocher, V ;
Fontaine, C ;
Torra, IP ;
Duhem, C ;
Kosykh, V ;
Fruchart, JC ;
Guillemette, C ;
Staels, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (16) :13975-13983
[6]   p38 mitogen-activated protein kinase activates peroxisome proliferator-activated receptor α -: A potential role in the cardiac metabolic stress response [J].
Barger, PM ;
Browning, AC ;
Garner, AN ;
Kelly, DP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (48) :44495-44501
[7]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[8]   The protein kinase C signaling pathway regulates a molecular switch between transactivation and transrepression activity of the peroxisome proliferator-activated receptor α [J].
Blanquart, C ;
Mansouri, R ;
Paumelle, R ;
Fruchart, JC ;
Staels, B ;
Glineur, C .
MOLECULAR ENDOCRINOLOGY, 2004, 18 (08) :1906-1918
[9]   Human microRNA genes are frequently located at fragile sites and genomic regions involved in cancers [J].
Calin, GA ;
Sevignani, C ;
Dan Dumitru, C ;
Hyslop, T ;
Noch, E ;
Yendamuri, S ;
Shimizu, M ;
Rattan, S ;
Bullrich, F ;
Negrini, M ;
Croce, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (09) :2999-3004
[10]   Most mammalian mRNAs are conserved targets of microRNAs [J].
Friedman, Robin C. ;
Farh, Kyle Kai-How ;
Burge, Christopher B. ;
Bartel, David P. .
GENOME RESEARCH, 2009, 19 (01) :92-105