HMEF2C GENE ENCODES SKELETAL MUSCLE-SPECIFIC AND BRAIN-SPECIFIC TRANSCRIPTION FACTORS

被引:206
作者
MCDERMOTT, JC
CARDOSO, MC
YU, YT
ANDRES, V
LEIFER, D
KRAINC, D
LIPTON, SA
NADALGINARD, B
机构
[1] CHILDRENS HOSP MED CTR,HOWARD HUGHES MED INST,BOSTON,MA 02115
[2] CHILDRENS HOSP MED CTR,DEPT CARDIOL,BOSTON,MA 02115
[3] HARVARD UNIV,SCH MED,DEPT CELLULAR & MOLEC PHYSIOL,BOSTON,MA 02115
[4] HARVARD UNIV,SCH MED,DEPT PEDIAT,BOSTON,MA 02115
[5] CHILDRENS HOSP MED CTR,DEPT NEUROL,BOSTON,MA 02115
关键词
D O I
10.1128/MCB.13.4.2564
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
The myocyte enhancer-binding factor 2 (MEF2) site is an essential element of many muscle-specific enhancers and promoters that binds nuclear proteins from muscle and brain. Recently, we have cloned a family of MEF2 transcription factors produced by two genes that, at the mRNA level, are broadly expressed and produce tissue-specific isoforms by posttranscriptional processes (Y.-T. Yu, R. E. Breitbart, L. B. Smoot, Y. Lee, V. Mahdavi, and B. Nadal-Ginard, Genes Dev. 6:1783-1798, 1992). Here, we report the isolation and functional characterization of cDNA clones encoding four MEF2 factors derived from a separate gene that we have named hMEF2C. In contrast to those of the previously reported genes, the transcripts of the hMEF2C gene are restricted to skeletal muscle and brain. One of the alternate exons is exclusively present in brain transcripts. The products of this gene have DNA-binding and trans-activating activities indistinguishable from those of the previously reported MEF2 factors. The hMEF2C gene is induced late during myogenic differentiation, and its expression is limited to a subset of cortical neurons. The potential targets for this transcription factor in a subset of neurons are not known at this time. The strict tissue-specific pattern of expression of hMEF2C in comparison with the more ubiquitous expression of other MEF2 genes suggests a different mode of regulation and a potentially important role of hMEF2C factors in myogenesis and neurogenesis.
引用
收藏
页码:2564 / 2577
页数:14
相关论文
共 54 条
  • [31] M-CAT BINDING-FACTOR, A NOVEL TRANS-ACTING FACTOR GOVERNING MUSCLE-SPECIFIC TRANSCRIPTION
    MAR, JH
    ORDAHL, CP
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (08) : 4271 - 4283
  • [32] TRANSCRIPTIONAL CONTROL SIGNALS OF A EUKARYOTIC PROTEIN-CODING GENE
    MCKNIGHT, SL
    KINGSBURY, R
    [J]. SCIENCE, 1982, 217 (4557) : 316 - 324
  • [33] THE PROLINE-RICH TRANSCRIPTIONAL ACTIVATOR OF CTF/NF-I IS DISTINCT FROM THE REPLICATION AND DNA-BINDING DOMAIN
    MERMOD, N
    ONEILL, EA
    KELLY, TJ
    TJIAN, R
    [J]. CELL, 1989, 58 (04) : 741 - 753
  • [34] THE SV40-72 BASE REPAIR REPEAT HAS A STRIKING EFFECT ON GENE-EXPRESSION BOTH IN SV40 AND OTHER CHIMERIC RECOMBINANTS
    MOREAU, P
    HEN, R
    WASYLYK, B
    EVERETT, R
    GAUB, MP
    CHAMBON, P
    [J]. NUCLEIC ACIDS RESEARCH, 1981, 9 (22) : 6047 - 6068
  • [35] Muscat George E. O., 1992, Gene Expression, V2, P111
  • [36] A SINGLE MEF-2 SITE IS A MAJOR POSITIVE REGULATORY ELEMENT REQUIRED FOR TRANSCRIPTION OF THE MUSCLE-SPECIFIC SUBUNIT OF THE HUMAN PHOSPHOGLYCERATE MUTASE GENE IN SKELETAL AND CARDIAC-MUSCLE-CELLS
    NAKATSUJI, Y
    HIDAKA, K
    TSUJINO, S
    YAMAMOTO, Y
    MUKAI, T
    YANAGIHARA, T
    KISHIMOTO, T
    SAKODA, S
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (10) : 4384 - 4390
  • [37] ISOLATION AND PROPERTIES OF CDNA CLONES ENCODING SRF, A TRANSCRIPTION FACTOR THAT BINDS TO THE C-FOS SERUM RESPONSE ELEMENT
    NORMAN, C
    RUNSWICK, M
    POLLOCK, R
    TREISMAN, R
    [J]. CELL, 1988, 55 (06) : 989 - 1003
  • [38] MYOD FAMILY - A PARADIGM FOR DEVELOPMENT - COMMENT
    OLSON, EN
    [J]. GENES & DEVELOPMENT, 1990, 4 (09) : 1454 - 1461
  • [39] PROMOTER SPECIFICITY OF BASAL TRANSCRIPTION FACTORS
    PARVIN, JD
    TIMMERS, HTM
    SHARP, PA
    [J]. CELL, 1992, 68 (06) : 1135 - 1144
  • [40] SACCHAROMYCES-CEREVISIAE PROTEIN INVOLVED IN PLASMID MAINTENANCE IS NECESSARY FOR MATING OF MAT-ALPHA CELLS
    PASSMORE, S
    MAINE, GT
    ELBLE, R
    CHRIST, C
    TYE, BK
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1988, 204 (03) : 593 - 606