The basic helix-loop-helix transcription factor Mist1 functions as a transcriptional repressor of MyoD

被引:96
作者
Lemercier, C [1 ]
To, RQ [1 ]
Carrasco, RA [1 ]
Konieczny, SD [1 ]
机构
[1] Purdue Univ, Dept Biol Sci, W Lafayette, IN 47907 USA
关键词
basic helix-loop-helix factors; E-proteins; gene regulation; MyoD; repressor proteins;
D O I
10.1093/emboj/17.5.1412
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
A good model system to examine aspects of positive and negative transcriptional regulation is the muscle-specific regulatory factor, MyoD, which is a basic helix-loop-helix (bHLH) transcription factor. Although MyoD has the ability to induce skeletal muscle terminal differentiation in a variety of non-muscle cell types, MyoD activity itself is highly regulated through protein-protein interactions involving several different cofactors, Here we describe the characterization of a novel bHLH protein, Mist1, and how it influences MyoD function, We show that Mist1 accumulates in myogenic stem cells (myoblasts) and then decreases as myoblasts differentiate into myotubes, Mist1 functions as a negative regulator of MyoD activity, preventing muscle differentiation and the concomitant expression of muscle-specific genes. Mist1-induced inhibition occurs through a combination of mechanisms, including the formation of inactive MyoD-Mist1 heterodimers and occupancy of specific E-box target sites by Mist1 homodimers. Mist1 lacks a classic transcription activation domain and instead possesses an N-terminal repressor region capable of inhibiting heterologous activators, Thus, Mist1 may represent a new class of repressor molecules that play a role in controlling the transcriptional activity of MyoD, ensuring that expanding myoblast populations remain undifferentiated during early embryonic muscle formation.
引用
收藏
页码:1412 / 1422
页数:11
相关论文
共 37 条
[1]  
AALLAND L, 1997, NATURE, V387, P49
[2]   MUSCLE LIM PROTEIN, A NOVEL ESSENTIAL REGULATOR OF MYOGENESIS, PROMOTES MYOGENIC DIFFERENTIATION [J].
ARBER, S ;
HALDER, G ;
CARONI, P .
CELL, 1994, 79 (02) :221-231
[3]   MAD-MAX TRANSCRIPTIONAL REPRESSION IS MEDIATED BY TERNARY COMPLEX-FORMATION WITH MAMMALIAN HOMOLOGS OF YEAST REPRESSOR SIN3 [J].
AYER, DE ;
LAWRENCE, QA ;
EISENMAN, RN .
CELL, 1995, 80 (05) :767-776
[4]   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
[5]   DIFFERENCES AND SIMILARITIES IN DNA-BINDING PREFERENCES OF MYOD AND E2A PROTEIN COMPLEXES REVEALED BY BINDING-SITE SELECTION [J].
BLACKWELL, TK ;
WEINTRAUB, H .
SCIENCE, 1990, 250 (4984) :1104-1110
[6]   CYTOPLASMIC ACTIVATION OF HUMAN NUCLEAR GENES IN STABLE HETEROCARYONS [J].
BLAU, HM ;
CHIU, CP ;
WEBSTER, C .
CELL, 1983, 32 (04) :1171-1180
[7]   MUSCLE - THE REGULATION OF MYOGENESIS [J].
BUCKINGHAM, ME .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1994, 4 (05) :745-751
[8]  
DAWSON SR, 1995, MOL CELL BIOL, V15, P6923
[9]  
Fisher AL, 1996, MOL CELL BIOL, V16, P2670
[10]   The basic domain of myogenic basic helix-loop-helix (bHLH) proteins is the novel target for direct inhibition by another bHLH protein, Twist [J].
Hamamori, Y ;
Wu, HY ;
Sartorelli, V ;
Kedes, L .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (11) :6563-6573