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
[1]   THE TRANSACTIVATING DOMAIN OF THE C-JUN PROTO-ONCOPROTEIN IS REQUIRED FOR COTRANSFORMATION OF RAT EMBRYO CELLS [J].
ALANI, R ;
BROWN, P ;
BINETRUY, B ;
DOSAKA, H ;
ROSENBERG, RK ;
ANGEL, P ;
KARIN, M ;
BIRRER, MJ .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (12) :6286-6295
[2]  
ANGEL P, 1989, New Biologist, V1, P35
[3]   THE JUN PROTO-ONCOGENE IS POSITIVELY AUTOREGULATED BY ITS PRODUCT, JUN/AP-1 [J].
ANGEL, P ;
HATTORI, K ;
SMEAL, T ;
KARIN, M .
CELL, 1988, 55 (05) :875-885
[4]   ONCOGENE JUN ENCODES A SEQUENCE-SPECIFIC TRANS-ACTIVATOR SIMILAR TO AP-1 [J].
ANGEL, P ;
ALLEGRETTO, EA ;
OKINO, ST ;
HATTORI, K ;
BOYLE, WJ ;
HUNTER, T ;
KARIN, M .
NATURE, 1988, 332 (6160) :166-171
[5]   PHORBOL ESTER INDUCIBLE GENES CONTAIN A COMMON CIS ELEMENT RECOGNIZED BY A TPA-MODULATED TRANS-ACTING FACTOR [J].
ANGEL, P ;
IMAGAWA, M ;
CHIU, R ;
STEIN, B ;
IMBRA, RJ ;
RAHMSDORF, HJ ;
JONAT, C ;
HERRLICH, P ;
KARIN, M .
CELL, 1987, 49 (06) :729-739
[6]   JUN - ONCOGENE AND TRANSCRIPTIONAL REGULATOR [J].
BALL, AR ;
BOS, TJ ;
LOLIGER, C ;
NAGATA, LP ;
NISHIMURA, T ;
SU, H ;
TSUCHIE, H ;
VOGT, PK .
COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1988, 53 :687-693
[7]   THE PROTEIN ID - A NEGATIVE REGULATOR OF HELIX-LOOP-HELIX DNA-BINDING PROTEINS [J].
BENEZRA, R ;
DAVIS, RL ;
LOCKSHON, D ;
TURNER, DL ;
WEINTRAUB, H .
CELL, 1990, 61 (01) :49-59
[8]   FUNCTIONAL ANTAGONISM BETWEEN C-JUN AND MYOD PROTEINS - A DIRECT PHYSICAL ASSOCIATION [J].
BENGAL, E ;
RANSONE, L ;
SCHARFMANN, R ;
DWARKI, VJ ;
TAPSCOTT, SJ ;
WEINTRAUB, H ;
VERMA, IM .
CELL, 1992, 68 (03) :507-519
[9]   HA-RAS AUGMENTS C-JUN ACTIVITY AND STIMULATES PHOSPHORYLATION OF ITS ACTIVATION DOMAIN [J].
BINETRUY, B ;
SMEAL, T ;
KARIN, M .
NATURE, 1991, 351 (6322) :122-127
[10]   THE PITUITARY-SPECIFIC TRANSCRIPTION FACTOR-GHF-1 IS A HOMEOBOX-CONTAINING PROTEIN [J].
BODNER, M ;
CASTRILLO, JL ;
THEILL, LE ;
DEERINCK, T ;
ELLISMAN, M ;
KARIN, M .
CELL, 1988, 55 (03) :505-518