Myocyte enhancer factor-related B-MEF2 is developmentally expressed in B cells and regulates the immunoglobulin J chain promoter

被引:32
作者
Rao, S
Karray, S
Gackstetter, ER
Koshland, ME
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Div Immunol, Berkeley, CA 94720 USA
[2] Inst Pasteur, Dept Immunol, F-75015 Paris, France
关键词
D O I
10.1074/jbc.273.40.26123
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
Immunoglobulin J chain gene expression is induced by the delivery of a lymphokine signal to antigen-activated B cells in a primary immune response. A major interleukin 2 (IL-2)-responsive region that contains two adjacent control elements (JA and JB) exists within the J chain promoter. Transcription factor PU.1 positively regulates J chain gene expression by binding to one of the control elements (JB) in the J chain promoter. In the present study we have determined that a myocyte enhancer factor 2 (MEF2)-related nuclear factor, named B-MEF2, positively regulates the J chain gene promoter activity via the second control element (JA), An in vitro translated MEF2 family member, MEF2C, was found to bind the JA site with identical properties as endogenously expressed B-MEF2 in B cell lines. Moreover, in vivo experiments showed that a dominant negative mutant of MEF2C blocked B-MEF2 regulation of the J chain promoter. Consistent with its role as positive regulator of J chain gene expression, B-MEF2 levels were enhanced in highly differentiated B cells. In addition, induction of an IL-2-responsive presecretor cell line BCL1 with IL-2 or IL-5 (which up-regulates J chain gene expression) resulted in an increased expression of B-MEF2. We conclude that a MEF2-related transcriptional factor, B-MEF2, acts as a stage-specific positive regulator of J chain gene expression in the B cell lineage.
引用
收藏
页码:26123 / 26129
页数:7
相关论文
共 37 条
[1]   THE MOUSE MRF4 PROMOTER IS TRANS-ACTIVATED DIRECTLY AND INDIRECTLY BY MUSCLE-SPECIFIC TRANSCRIPTION FACTORS [J].
BLACK, BL ;
MARTIN, JF ;
OLSON, EN .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (07) :2889-2892
[2]  
BLACKMAN M, 1986, CELL, V46, P609
[3]  
BREITBART RE, 1993, DEVELOPMENT, V118, P1095
[4]   MUSCLE-SPECIFIC EXPRESSION OF SRF-RELATED GENES IN THE EARLY EMBRYO OF XENOPUS-LAEVIS [J].
CHAMBERS, AE ;
KOTECHA, S ;
TOWERS, N ;
MOHUN, TJ .
EMBO JOURNAL, 1992, 11 (13) :4981-4991
[5]   ACTIVATION OF MAP KINASE KINASE IS NECESSARY AND SUFFICIENT FOR PC12 DIFFERENTIATION AND FOR TRANSFORMATION OF NIH 3T3 CELLS [J].
COWLEY, S ;
PATERSON, H ;
KEMP, P ;
MARSHALL, CJ .
CELL, 1994, 77 (06) :841-852
[6]  
DAVIS RJ, 1993, J BIOL CHEM, V268, P14553
[7]  
DODUO E, 1995, NUCLEIC ACIDS RES, V23, P4267
[8]  
EDMONDSON DG, 1994, DEVELOPMENT, V120, P1251
[9]   A NEW MYOCYTE-SPECIFIC ENHANCER-BINDING FACTOR THAT RECOGNIZES A CONSERVED ELEMENT ASSOCIATED WITH MULTIPLE MUSCLE-SPECIFIC GENES [J].
GOSSETT, LA ;
KELVIN, DJ ;
STERNBERG, EA ;
OLSON, EN .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (11) :5022-5033
[10]   CELL-TYPE SPECIFICITY OF IMMUNOGLOBULIN GENE-EXPRESSION IS REGULATED BY AT LEAST 3 DNA-SEQUENCE ELEMENTS [J].
GROSSCHEDL, R ;
BALTIMORE, D .
CELL, 1985, 41 (03) :885-897