Cardiac ankyrin repeat protein, a negative regulator of cardiac gene expression, is augmented in human heart failure

被引:77
作者
Zolk, O
Frohme, M
Maurer, A
Kluxen, FW
Hentsch, B
Zubakov, D
Hoheisel, JD
Zucker, IH
Pepe, S
Eschenhagen, T
机构
[1] Univ Erlangen Nurnberg, Inst Expt & Klin Pharmakol & Toxikol, D-91054 Erlangen, Germany
[2] Deutsch Krebsforschungszentrum, D-6900 Heidelberg, Germany
[3] Merck KGaA, Darmstadt, Germany
[4] Univ Nebraska, Coll Med, Dept Physiol & Biophys, Omaha, NE 68198 USA
[5] Alfred Hosp, Cardiac Surg Res Unit, Melbourne, Vic, Australia
[6] Baker Med Res Inst, Melbourne, Vic, Australia
关键词
CARP; representational difference analysis of cDNA; gene expression; cardiac muscle; ischemic cardiomyopathy; dilated cardiomyopathy; heart failure;
D O I
10.1016/S0006-291X(02)00387-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The technique of representational difference analysis of cDNA has been applied to screen for differentially expressed genes in a canine model of pacing-induced heart failure. We identified the canine homolog of the cardiac ankyrin repeat protein (CARP) which has been shown to be involved in the regulation of the transcription of cardiac genes. To confirm the significance for human heart failure, cardiac tissue specimens obtained from non-failing donor hearts and from explanted hearts from patients with end-stage heart failure were investigated. CARP mRNA and protein levels were markedly increased in failing left ventricles. Interestingly, alterations in CARP expression were restricted to ventricular tissue and were not observed in atria. Fractionation experiments revealed that CARP was expressed predominantly in the nuclei consistent with the proposed function of CARP as a modulator of transcription. Together, these findings raise the possibility that augmented ventricular CARP expression may play a role in the pathogenesis of human heart failure. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:1377 / 1382
页数:6
相关论文
共 19 条
[1]   Doxorubicin represses CARP gene transcription through the generation of oxidative stress in neonatal rat cardiac myocytes: Possible role of serine/threonine kinase-dependent pathways [J].
Aihara, Y ;
Kurabayashi, M ;
Tanaka, T ;
Takeda, S ;
Tomaru, K ;
Sekiguchi, K ;
Ohyama, Y ;
Nagai, R .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2000, 32 (08) :1401-1414
[2]   Accumulation of muscle ankyrin repeat protein transcript reveals local activation of primary myotube endcompartments during muscle morphogenesis [J].
Baumeister, A ;
Arber, S ;
Caroni, P .
JOURNAL OF CELL BIOLOGY, 1997, 139 (05) :1231-1242
[3]   IDENTIFICATION AND CHARACTERIZATION OF A NOVEL CYTOKINE-INDUCIBLE NUCLEAR-PROTEIN FROM HUMAN ENDOTHELIAL-CELLS [J].
CHU, W ;
BURNS, DK ;
SWERLICK, RA ;
PRESKY, DH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (17) :10236-10245
[4]  
Frohme M, 2000, ANN NY ACAD SCI, V910, P85
[5]   IDENTIFYING DIFFERENCES IN MESSENGER-RNA EXPRESSION BY REPRESENTATIONAL DIFFERENCE ANALYSIS OF CDNA [J].
HUBANK, M ;
SCHATZ, DG .
NUCLEIC ACIDS RESEARCH, 1994, 22 (25) :5640-5648
[6]  
Hubank M, 1999, METHOD ENZYMOL, V303, P325
[7]   A novel cardiac-restricted target for doxorubicin - CARP, a nuclear modulator of gene expression in cardiac progenitor cells and cardiomyocytes [J].
Jeyaseelan, R ;
Poizat, C ;
Baker, RK ;
Abdishoo, S ;
Isterabadi, LB ;
Lyons, GE ;
Kedes, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (36) :22800-22808
[8]   Transforming growth factor-β/Smads signaling induces transcription of the cell type-restricted ankyrin repeat protein CARP gene through CAGA motif in vascular smooth muscle cells [J].
Kanai, H ;
Tanaka, T ;
Aihara, Y ;
Takeda, S ;
Kawabata, M ;
Miyazono, K ;
Nagai, R ;
Kurabayashi, M .
CIRCULATION RESEARCH, 2001, 88 (01) :30-36
[9]   Functional genomics and cardiovascular drug discovery [J].
Lee, RT .
CIRCULATION, 2001, 104 (12) :1441-1446
[10]   Reduced NO enhances the central gain of cardiac sympathetic afferent reflex in dogs with heart failure [J].
Ma, R ;
Zucker, IH ;
Wang, W .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1999, 276 (01) :H19-H26