Regulation of connexin expression

被引:144
作者
Oyamada, M [1 ]
Oyamada, Y
Takamatsu, T
机构
[1] Kyoto Prefectural Univ Med, Dept Pathol & Cell Regulat, Kamigyo Ku, Kyoto 6028566, Japan
[2] Meiji Univ Oriental Med, Dept Pathol, Kyoto, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2005年 / 1719卷 / 1-2期
关键词
connexin; gap junction; gene regulation; alternative splicing; transcription factor;
D O I
10.1016/j.bbamem.2005.11.002
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
Gap junctions contain cell-cell communicating channels that consist of multimeric proteins called connexins and mediate the exchange of low-molecular-weight metabolites and ions between contacting cells. Gap junctional communication has long been hypothesized to play a crucial role in the maintenance of homeostasis, morphogenesis, cell differentiation, and growth control in multicellular organisms. The recent discovery that human genetic disorders are associated with mutations in connexin genes and experimental data on connexin knockout mice have provided direct evidence that gap junctional communication is essential for tissue functions and organ development. Thus far, 21 human genes and 20 mouse genes for connexins have been identified. Each connexin shows tissue- or cell-type-specific expression, and most organs and many cell types express more than one connexin. Cell coupling via gap junctions is dependent on the specific pattern of connexin gene expression. This pattern of gene expression is altered during development and in several pathological conditions resulting in changes of cell coupling. Connexin expression can be regulated at many of the steps in the pathway from DNA to RNA to protein. However, transcriptional control is one of the most important points. In this review, we summarize recent knowledge on transcriptional regulation of connexin genes by describing the structure of connexin genes and transcriptional factors that regulate connexin expression. (C) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:6 / 23
页数:18
相关论文
共 127 条
[11]   Chamber-specific cardiac expression of Tbx5 and heart defects in Holt-Oram syndrome [J].
Bruneau, BG ;
Logan, M ;
Davis, N ;
Levi, T ;
Tabin, CJ ;
Seidman, JG ;
Seidman, CE .
DEVELOPMENTAL BIOLOGY, 1999, 211 (01) :100-108
[12]   Transcriptional regulation of vertebrate cardiac morphogenesis [J].
Bruneau, BG .
CIRCULATION RESEARCH, 2002, 90 (05) :509-519
[13]   A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease [J].
Bruneau, BG ;
Nemer, G ;
Schmitt, JP ;
Charron, F ;
Robitaille, L ;
Caron, S ;
Conner, DA ;
Gessler, M ;
Nemer, M ;
Seidman, CE ;
Seidman, JG .
CELL, 2001, 106 (06) :709-721
[14]   Unexpected induction of the human connexin 43 promoter by the Ras signaling pathway is mediated by a novel putative promoter sequence [J].
Carystinos, GD ;
Kandouz, M ;
Alaoui-Jamali, MA ;
Batist, G .
MOLECULAR PHARMACOLOGY, 2003, 63 (04) :821-831
[15]   A GENE ENCODING A PROTEIN WITH ZINC FINGERS IS ACTIVATED DURING G0/G1 TRANSITION IN CULTURED-CELLS [J].
CHAVRIER, P ;
ZERIAL, M ;
LEMAIRE, P ;
ALMENDRAL, J ;
BRAVO, R ;
CHARNAY, P .
EMBO JOURNAL, 1988, 7 (01) :29-35
[16]   THE SEGMENT-SPECIFIC GENE KROX-20 ENCODES A TRANSCRIPTION FACTOR WITH BINDING-SITES IN THE PROMOTER REGION OF THE HOX-1.4 GENE [J].
CHAVRIER, P ;
VESQUE, C ;
GALLIOT, B ;
VIGNERON, M ;
DOLLE, P ;
DUBOULE, D ;
CHARNAY, P .
EMBO JOURNAL, 1990, 9 (04) :1209-1218
[17]   Tbx2 represses expression of Connexin43 in osteoblastic-like cells [J].
Chen, JR ;
Chatterjee, B ;
Meyer, R ;
Yu, JC ;
Borke, JL ;
Isales, CM ;
Kirby, ML ;
Lo, CW ;
Bollag, RJ .
CALCIFIED TISSUE INTERNATIONAL, 2004, 74 (06) :561-573
[18]  
Chen JT, 2003, CLIN CANCER RES, V9, P4200
[19]   CERAMIDE REVERSES BREFELDIN-A (BFA) RESISTANCE IN BFA-RESISTANT CELL-LINES [J].
ODA, T ;
CHEN, CH ;
WU, HC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (08) :4088-4092
[20]   EXPRESSION OF THE GAP JUNCTION PROTEIN CONNEXIN-43 IS INCREASED IN THE HUMAN MYOMETRIUM TOWARD TERM AND WITH THE ONSET OF LABOR [J].
CHOW, L ;
LYE, SJ .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1994, 170 (03) :788-795