PEBP2/PEA2 REPRESENTS A FAMILY OF TRANSCRIPTION FACTORS HOMOLOGOUS TO THE PRODUCTS OF THE DROSOPHILA RUNT GENE AND THE HUMAN AML1 GENE

被引:574
作者
OGAWA, E
MARUYAMA, M
KAGOSHIMA, H
INUZUKA, M
LU, J
SATAKE, M
SHIGESADA, K
ITO, Y
机构
[1] KYOTO UNIV,INST VIRUS RES,DEPT VIRAL ONCOL,SAKYO KU,KYOTO 606,JAPAN
[2] KYOTO UNIV,INST VIRUS RES,DEPT GENET & MOLEC BIOL,SAKYO KU,KYOTO 606,JAPAN
关键词
T-CELL RECEPTOR; EARLY DEVELOPMENT; ACUTE MYELOID LEUKEMIA; T(8,21); DNA BINDING AND DIMERIZATION DOMAIN;
D O I
10.1073/pnas.90.14.6859
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
cDNAs representing the alpha subunit of polyomavirus enhancer binding protein 2 (PEBP2; also called PEA2) were isolated. The products of the cDNAs are highly homologous to that of Drosophila segmentation gene runt (run) for an N-proximal 128-amino acid region showing 66% identity. The run homology region encompasses the domain capable of binding to a specific nucleotide sequence motif and of dimerizing with the companion beta subunit. The human AML1 gene related to t(8;21) acute myeloid leukemia also has a run homology region. Together with the beta subunit, which increases the affinity of the alpha subunit to DNA without binding to DNA by itself, PEBP2 represents a newly discovered family of transcription factor. The major species of PEBP2alpha mRNA was expressed in T-cell lines but not in B-cell lines tested. Evidence indicated that PEBP2 functions as a transcriptional activator and is involved in regulation of T-cell-specific gene expression.
引用
收藏
页码:6859 / 6863
页数:5
相关论文
共 26 条
[1]   A POLYOMAVIRUS ENHANCER-BINDING PROTEIN, PEBP5, RESPONSIVE TO 12-O-TETRADECANOYLPHORBOL-13-ACETATE BUT DISTINCT FROM AP-1 [J].
ASANO, M ;
MURAKAMI, Y ;
FURUKAWA, K ;
YAMAGUCHIIWAI, Y ;
SATAKE, M ;
ITO, Y .
JOURNAL OF VIROLOGY, 1990, 64 (12) :5927-5938
[2]   EXPRESSION OF POLYOMA-VIRUS IN HETEROKARYONS BETWEEN EMBRYONAL CARCINOMA CELLS AND DIFFERENTIATED CELLS [J].
BOCCARA, M ;
KELLY, F .
VIROLOGY, 1978, 90 (01) :147-150
[3]   HIGH-EFFICIENCY TRANSFORMATION OF MAMMALIAN-CELLS BY PLASMID DNA [J].
CHEN, C ;
OKAYAMA, H .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (08) :2745-2752
[4]   MUTATION NEAR THE POLYOMA DNA-REPLICATION ORIGIN PERMITS PRODUCTIVE INFECTION OF F9 EMBRYONAL CARCINOMA-CELLS [J].
FUJIMURA, FK ;
DEININGER, PL ;
FRIEDMANN, T ;
LINNEY, E .
CELL, 1981, 23 (03) :809-814
[5]  
FURUKAWA K, 1990, CELL GROWTH DIFFER, V1, P135
[6]   ALIGNMENT OF U3 REGION SEQUENCES OF MAMMALIAN TYPE-C VIRUSES - IDENTIFICATION OF HIGHLY CONSERVED MOTIFS AND IMPLICATIONS FOR ENHANCER DESIGN [J].
GOLEMIS, EA ;
SPECK, NA ;
HOPKINS, N .
JOURNAL OF VIROLOGY, 1990, 64 (02) :534-542
[7]   IDENTIFICATION AND FUNCTIONAL-CHARACTERIZATION OF THE HUMAN T-CELL RECEPTOR BETA-GENE TRANSCRIPTIONAL ENHANCER - COMMON NUCLEAR PROTEINS INTERACT WITH THE TRANSCRIPTIONAL REGULATORY ELEMENTS OF THE T-CELL RECEPTOR ALPHA-GENE AND BETA-GENE [J].
GOTTSCHALK, LR ;
LEIDEN, JM .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (10) :5486-5495
[8]   PURIFICATION OF A MOUSE NUCLEAR FACTOR THAT BINDS TO BOTH THE A AND B CORES OF THE POLYOMAVIRUS ENHANCER [J].
KAMACHI, Y ;
OGAWA, E ;
ASANO, M ;
ISHIDA, S ;
MURAKAMI, Y ;
SATAKE, M ;
ITO, Y ;
SHIGESADA, K .
JOURNAL OF VIROLOGY, 1990, 64 (10) :4808-4819
[9]   THE DROSOPHILA SEGMENTATION GENE RUNT ENCODES A NOVEL NUCLEAR REGULATORY PROTEIN THAT IS ALSO EXPRESSED IN THE DEVELOPING NERVOUS-SYSTEM [J].
KANIA, MA ;
BONNER, AS ;
DUFFY, JB ;
GERGEN, JP .
GENES & DEVELOPMENT, 1990, 4 (10) :1701-1713
[10]   POLYOMA DNA-SEQUENCES INVOLVED IN CONTROL OF VIRAL GENE-EXPRESSION IN MURINE EMBRYONAL CARCINOMA-CELLS [J].
KATINKA, M ;
VASSEUR, M ;
MONTREAU, N ;
YANIV, M ;
BLANGY, D .
NATURE, 1981, 290 (5808) :720-722