Induced ICER Iγ down-regulates cyclin A expression and cell proliferation in insulin-producing β cells

被引:23
作者
Inada, A [1 ]
Weir, GC [1 ]
Bonner-Weir, S [1 ]
机构
[1] Harvard Univ, Sch Med, Joslin Diabet Ctr, Sect Islet Transplantat & Cell Biol, Boston, MA 02215 USA
关键词
cyclic AMP-responsive element; ICER; cyclin A;
D O I
10.1016/j.bbrc.2005.02.046
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
We have previously found that cyclin A expression is markedly reduced in pancreatic beta-cells by cell-specific overexpression of repressor inducible cyclic AMP early repressor (ICER I gamma) in transgenic mice. Here we further examined regulatory effects of ICER I gamma on cyclin A gene expression using Min6 cells, an insulin-producing cell line. The cyclin A promoter luciferase assay showed that ICER I gamma directly repressed cyclin A gene transcription. In addition, upon ICER I gamma overexpression, cyclin A mRNA levels markedly decreased, thereby confirming an inhibitory effect of ICER I gamma on cyclin A expression. Suppression of cyclin A results in inhibition of BrdU incorporation. Under normal culture conditions endogenous cyclin A is abundant in these cells, whereas ICER is hardly detectable. However, serum starvation of Min6 cells induces ICER I gamma expression with a concomitant very low expression level of cyclin A. Cyclin A protein is not expressed unless the cells are in active DNA replication. These results indicate a potentially important anti-proliferative effect of ICER I gamma in pancreatic beta cells. Since ICER I gamma is greatly increased in diabetes as well as in FFA- or high glucose-treated islets, this effect may in part exacerbate diabetes by limiting beta-cell proliferation. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:925 / 929
页数:5
相关论文
共 34 条
[21]   Overexpression of inducible cyclic AMP early repressor inhibits transactivation of genes and cell proliferation in pancreatic β cells [J].
Inada, A ;
Hamamoto, Y ;
Tsuura, Y ;
Miyazaki, J ;
Toyokuni, S ;
Ihara, Y ;
Nagai, K ;
Yamada, Y ;
Bonner-Weir, S ;
Seino, Y .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (07) :2831-2841
[22]  
ISHII S, 1990, ADV 2 MESSENGER PHOS, V24, P335
[23]   LEUCINE ZIPPER STRUCTURE OF THE PROTEIN CRE-BP1 BINDING TO THE CYCLIC-AMP RESPONSE ELEMENT IN BRAIN [J].
MAEKAWA, T ;
SAKURA, H ;
KANEIISHII, C ;
SUDO, T ;
YOSHIMURA, T ;
FUJISAWA, J ;
YOSHIDA, M ;
ISHII, S .
EMBO JOURNAL, 1989, 8 (07) :2023-2028
[24]   INDUCIBILITY AND NEGATIVE AUTOREGULATION OF CREM - AN ALTERNATIVE PROMOTER DIRECTS THE EXPRESSION OF ICER, AN EARLY RESPONSE REPRESSOR [J].
MOLINA, CA ;
FOULKES, NS ;
LALLI, E ;
SASSONECORSI, P .
CELL, 1993, 75 (05) :875-886
[25]   THE CDC2 KINASE IS A NUCLEAR-PROTEIN THAT IS ESSENTIAL FOR MITOSIS IN MAMMALIAN-CELLS [J].
RIABOWOL, K ;
DRAETTA, G ;
BRIZUELA, L ;
VANDRE, D ;
BEACH, D .
CELL, 1989, 57 (03) :393-401
[26]  
ROSENBERG AR, 1995, ONCOGENE, V10, P1501
[27]   CELL-CYCLE REGULATION OF THE CYCLIN-A GENE PROMOTER IS MEDIATED BY A VARIANT E2F SITE [J].
SCHULZE, A ;
ZERFASS, K ;
SPITKOVSKY, D ;
MIDDENDORP, S ;
BERGES, J ;
HELIN, K ;
JANSENDURR, P ;
HENGLEIN, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (24) :11264-11268
[28]   A novel immunohistochemical method to estimate cell-cycle phase distribution in archival tissue: implications for the prediction of outcome in colorectal cancer [J].
Scott, IS ;
Morris, LS ;
Bird, K ;
Davies, RJ ;
Vowler, SL ;
Rushbrook, SM ;
Marshall, AE ;
Laskey, RA ;
Miller, R ;
Arends, MJ ;
Coleman, N .
JOURNAL OF PATHOLOGY, 2003, 201 (02) :187-197
[29]   Activation of the rat cyclin a promoter by ATF2 and Jun family members and its suppression by ATF4 [J].
Shimizu, M ;
Nomura, Y ;
Suzuki, K ;
Ichikawa, E ;
Takeuchi, A ;
Suzuki, M ;
Nakamura, T ;
Nakajima, T ;
Oda, K .
EXPERIMENTAL CELL RESEARCH, 1998, 239 (01) :93-103
[30]   Cyclin A in cell cycle control and cancer [J].
Yam, CH ;
Fung, TK ;
Poon, RYC .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2002, 59 (08) :1317-1326