FOS AND JUN REPRESS TRANSCRIPTIONAL ACTIVATION BY MYOGENIN AND MYOD - THE AMINO TERMINUS OF JUN CAN MEDIATE REPRESSION

被引:240
作者
LI, L
CHAMBARD, JC
KARIN, M
OLSON, EN
机构
[1] UNIV TEXAS, MD ANDERSON CANC CTR, DEPT BIOCHEM & MOLEC BIOL, HOUSTON, TX 77030 USA
[2] UNIV CALIF SAN DIEGO, SCH MED, CTR MOLEC GENET, DEPT PHARMACOL, LA JOLLA, CA 92093 USA
关键词
MYOGENIN; MYOD; TRANSCRIPTIONAL ACTIVATION; MYOGENESIS; HLH PROTEINS;
D O I
10.1101/gad.6.4.676
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Myogenin and MyoD belong to a family of muscle-specific helix-loop-helix (HLH) proteins that have the potential to activate muscle-specific genes in nonmyogenic cells. Peptide growth factors can block the ability of myogenin and MyoD to activate their target genes. Here, we show that the growth factor-inducible proto-oncogenes c-fos, c-jun, and junB mimic the effects of exogenous growth factors and suppress trans-activation of the muscle creatine kinase (MCK) enhancer by myogenin and MyoD. In contrast, JunD, which shares DNA-binding specificity with JunB and c-Jun but is expressed constitutively in muscle cells, is an inefficient inhibitor of the trans-activating capacity of myogenin and MyoD. Transcriptional repression by Fos and Jun is specific to myogenic HLH proteins and is not observed with the widely expressed HLH protein E47, which recognizes the same DNA sequence. Repression of the MCK enhancer by Fos and Jun is targeted at the myogenin and MyoD DNA recognition sequence and can be mediated by the amino terminus of c-Jun. Comparison of several myogenin mutants for their responsiveness to Fos and Jun shows that repression is directed at the basic-HLH region. These results indicate that members of the Jun family can be distinguished on the basis of their effects on muscle-specific transcription and suggest there is cross talk between transcription factors that control myogenesis and those involved in cell proliferation.
引用
收藏
页码:676 / 689
页数:14
相关论文
共 71 条
[31]   2 DISTINCT TRANSCRIPTION FACTORS THAT BIND THE IMMUNOGLOBULIN ENHANCER MU-E5/KE2 MOTIF [J].
HENTHORN, P ;
KILEDJIAN, M ;
KADESCH, T .
SCIENCE, 1990, 247 (4941) :467-470
[32]  
HU JS, 1988, J BIOL CHEM, V263, P19670
[33]   TRANSCRIPTION FACTOR AP-2 MEDIATES INDUCTION BY 2 DIFFERENT SIGNAL-TRANSDUCTION PATHWAYS - PROTEIN-KINASE-C AND CAMP [J].
IMAGAWA, M ;
CHIU, R ;
KARIN, M .
CELL, 1987, 51 (02) :251-260
[34]   A HARVEY-RAS RESPONSIVE TRANSCRIPTION ELEMENT IS ALSO RESPONSIVE TO A TUMOR-PROMOTER AND TO SERUM [J].
IMLER, JL ;
SCHATZ, C ;
WASYLYK, C ;
CHATTON, B ;
WASYLYK, B .
NATURE, 1988, 332 (6161) :275-278
[35]   TRANSCRIPTIONAL REGULATION OF THE MUSCLE CREATINE-KINASE GENE AND REGULATED EXPRESSION IN TRANSFECTED MOUSE MYOBLASTS [J].
JAYNES, JB ;
CHAMBERLAIN, JS ;
BUSKIN, JN ;
JOHNSON, JE ;
HAUSCHKA, SD .
MOLECULAR AND CELLULAR BIOLOGY, 1986, 6 (08) :2855-2864
[36]   ANTITUMOR PROMOTION AND ANTIINFLAMMATION - DOWN-MODULATION OF AP-1 (FOS JUN) ACTIVITY BY GLUCOCORTICOID HORMONE [J].
JONAT, C ;
RAHMSDORF, HJ ;
PARK, KK ;
CATO, ACB ;
GEBEL, S ;
PONTA, H ;
HERRLICH, P .
CELL, 1990, 62 (06) :1189-1204
[37]  
KARIN M, 1990, MOL ASPECTS CELLULAR, V6, P143
[38]   AUTO-REGULATION OF FOS - THE DYAD SYMMETRY ELEMENT AS THE MAJOR TARGET OF REPRESSION [J].
KONIG, H ;
PONTA, H ;
RAHMSDORF, U ;
BUSCHER, M ;
SCHONTHAL, A ;
RAHMSDORF, HJ ;
HERRLICH, P .
EMBO JOURNAL, 1989, 8 (09) :2559-2566
[39]   MYOD IS A SEQUENCE-SPECIFIC DNA-BINDING PROTEIN REQUIRING A REGION OF MYC HOMOLOGY TO BIND TO THE MUSCLE CREATINE-KINASE ENHANCER [J].
LASSAR, AB ;
BUSKIN, JN ;
LOCKSHON, D ;
DAVIS, RL ;
APONE, S ;
HAUSCHKA, SD ;
WEINTRAUB, H .
CELL, 1989, 58 (05) :823-831
[40]   FUNCTIONAL-ACTIVITY OF MYOGENIC HLH PROTEINS REQUIRES HETERO-OLIGOMERIZATION WITH E12/E47-LIKE PROTEINS INVIVO [J].
LASSAR, AB ;
DAVIS, RL ;
WRIGHT, WE ;
KADESCH, T ;
MURRE, C ;
VORONOVA, A ;
BALTIMORE, D ;
WEINTRAUB, H .
CELL, 1991, 66 (02) :305-315