MRG15, a novel chromodomain protein, is present in two distinct multiprotein complexes involved in transcriptional activation

被引:69
作者
Pardo, PS
Leung, JK
Lucchesi, JC
Pereira-Smith, OM
机构
[1] Baylor Coll Med, Roy M & Phyllis Gough Huffington Ctr Aging, Houston, TX 77030 USA
[2] Emory Univ, Dept Biol, Atlanta, GA 30322 USA
关键词
D O I
10.1074/jbc.M203839200
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
MRG15 is a novel chromodomain protein that is a member of a family of genes related to MORF4. MORF4 (mortality factor on chromosome 4) induces senescence in a subset of human tumor cell lines. Our previous results indicated that MRG15 (MORF-related gene on chromosome 15) could derepress the B-myb promoter by association with Rb. In this study, sucrose gradient analysis demonstrated that MRG15 was present in two distinct nuclear protein complexes, MAF1 (MRG15-associated factor 1) and MAF2.. Rb was associated with MRG15 and PAM14 (a novel coil-coil protein) in MAF1, and a histone acetyl transferase, hMOF, was an MRG15 partner in MAF2. Analysis of deletion mutants of MRG15 indicated that the leucine zipper at the C-terminal region of MRG15 was important for the protein associations in MAF1 and that the N-terminal chromodomain was required for the assembly of the MAF2 protein complex. Consistent with these data was the fact that a histone acetyltransferase activity associated with MRG15 was lost when the chromodomain was deleted and that both mutant MRG15 proteins failed to activate the B-myb promoter. The various mechanisms by which MRG15 could activate gene transcription are discussed.
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收藏
页码:50860 / 50866
页数:7
相关论文
共 26 条
[1]   Chromodomains are protein-RNA interaction modules [J].
Akhtar, A ;
Zink, D ;
Becker, PB .
NATURE, 2000, 407 (6802) :405-409
[2]   Structure of the chromatin binding (chromo) domain from mouse modifier protein 1 [J].
Ball, LJ ;
Murzina, NV ;
Broadhurst, RW ;
Raine, ARC ;
Archer, SJ ;
Stott, FJ ;
Murzin, AG ;
Singh, PB ;
Domaille, PJ ;
Laue, ED .
EMBO JOURNAL, 1997, 16 (09) :2473-2481
[3]  
Bertram MJ, 1999, MOL CELL BIOL, V19, P1479
[4]   Conservation of the MORF4 related gene family:: identification of a new chromo domain subfamily and novel protein motif [J].
Bertram, MJ ;
Pereira-Smith, OM .
GENE, 2001, 266 (1-2) :111-121
[5]   Self-association of chrome domain peptides [J].
Cowell, IG ;
Austin, CA .
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY, 1997, 1337 (02) :198-206
[6]   The yeast NuA4 and Drosophila MSL complexes contain homologous subunits important for transcription regulation [J].
Eisen, A ;
Utley, RT ;
Nourani, A ;
Allard, S ;
Schmidt, P ;
Lane, WS ;
Lucchesi, JC ;
Côté, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (05) :3484-3491
[7]  
GORMAN M, 1995, DEVELOPMENT, V121, P463
[8]   REGULATION OF THE SEX-SPECIFIC BINDING OF THE MALELESS DOSAGE COMPENSATION PROTEIN TO THE MALE X-CHROMOSOME IN DROSOPHILA [J].
GORMAN, M ;
KURODA, MI ;
BAKER, BS .
CELL, 1993, 72 (01) :39-49
[9]  
Hatakeyama M, 1995, Prog Cell Cycle Res, V1, P9
[10]   mof, a putative acetyl transferase gene related to the Tip60 and MOZ human genes and to the SAS genes of yeast, is required for dosage compensation in Drosophila [J].
Hilfiker, A ;
HilfikerKleiner, D ;
Pannuti, A ;
Lucchesi, JC .
EMBO JOURNAL, 1997, 16 (08) :2054-2060