ASSOCIATION OF THE PROTEIN-KINASES C-BCR AND BCR-ABL WITH PROTEINS OF THE 14-3-3-FAMILY

被引:217
作者
REUTHER, GW
FU, H
CRIPE, LD
COLLIER, RJ
PENDERGAST, AM
机构
[1] DUKE UNIV, MED CTR, DEPT PHARMACOL, DURHAM, NC 27710 USA
[2] HARVARD UNIV, SCH MED, DEPT MICROBIOL & MOLEC GENET, BOSTON, MA 02115 USA
[3] HARVARD UNIV, SCH MED, SHIPLEY INST MED, BOSTON, MA 02115 USA
关键词
D O I
10.1126/science.7939633
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
In this study, a protein that interacts with sequences encoded by the first exon of the protein kinase Bcr was cloned. The Bcr-associated protein 1 (Bap-1) is a member of the 14-3-3 family of proteins. Bap-1 interacts with full-length c-Bcr and with the chimeric Bcr-Abl tyrosine kinase of Philadelphia chromosome (Ph(1))-positive human leukemias. Bap-1 is a substrate for the Bcr serine-threonine kinase and is also phosphorylated on tyrosine by Bcr-Abl but not by c-Abl. Bap-1 may function in the regulation of c-Bcr and may contribute to the transforming activity of Bcr-Abl in vivo. 14-3-3 proteins are essential for cell proliferation and have a role in determining the timing of mitosis in yeast. Through direct binding to sequences present in Bcr and in other proteins implicated in signaling, the mammalian 14-3-3 proteins may link specific signaling protein components to mitogenic and cell-cycle control pathways.
引用
收藏
页码:129 / 133
页数:5
相关论文
共 39 条
[21]  
MORRISON DK, 1990, CANCER CELL-MON REV, V2, P377
[22]   BCR 1ST EXON SEQUENCES SPECIFICALLY ACTIVATE THE BCR ABL TYROSINE KINASE ONCOGENE OF PHILADELPHIA CHROMOSOME-POSITIVE HUMAN LEUKEMIAS [J].
MULLER, AJ ;
YOUNG, JC ;
PENDERGAST, AM ;
PONDEL, M ;
LANDAU, NR ;
LITTMAN, DR ;
WITTE, ON .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (04) :1785-1792
[23]   THE PH DOMAIN - A COMMON PIECE IN THE STRUCTURAL PATCHWORK OF SIGNALING PROTEINS [J].
MUSACCHIO, A ;
GIBSON, T ;
RICE, P ;
THOMPSON, J ;
SARASTE, M .
TRENDS IN BIOCHEMICAL SCIENCES, 1993, 18 (09) :343-348
[24]   PRIMARY STRUCTURE OF A HUMAN PROTEIN-KINASE REGULATOR PROTEIN [J].
NIELSEN, PJ .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1088 (03) :425-428
[25]   ASSOCIATION OF POLYOMAVIRUS MIDDLE TUMOR-ANTIGEN WITH 14-3-3-PROTEINS [J].
PALLAS, DC ;
FU, H ;
HAEHNEL, LC ;
WELLER, W ;
COLLIER, RJ ;
ROBERTS, TM .
SCIENCE, 1994, 265 (5171) :535-537
[26]   SH1 DOMAIN AUTOPHOSPHORYLATION OF P210 BCR ABL IS REQUIRED FOR TRANSFORMATION BUT NOT GROWTH-FACTOR INDEPENDENCE [J].
PENDERGAST, AM ;
GISHIZKY, ML ;
HAVLIK, MH ;
WITTE, ON .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (03) :1728-1736
[27]   BCR-ABL-INDUCED ONCOGENESIS IS MEDIATED BY DIRECT INTERACTION WITH THE SH2 DOMAIN OF THE GRB-2 ADAPTER PROTEIN [J].
PENDERGAST, AM ;
QUILLIAM, LA ;
CRIPE, LD ;
BASSING, CH ;
DAI, ZH ;
LI, NX ;
BATZER, A ;
RABUN, KM ;
DER, CJ ;
SCHLESSINGER, J ;
GISHIZKY, ML .
CELL, 1993, 75 (01) :175-185
[28]   BCR SEQUENCES ESSENTIAL FOR TRANSFORMATION BY THE BCR-ABL ONCOGENE BIND TO THE ABL-SH2 REGULATORY DOMAIN IN A NON-PHOSPHOTYROSINE-DEPENDENT MANNER [J].
PENDERGAST, AM ;
MULLER, AJ ;
HAVLIK, MH ;
MARU, Y ;
WITTE, ON .
CELL, 1991, 66 (01) :161-171
[29]   BCR-ABL ONCOPROTEINS BIND DIRECTLY TO ACTIVATORS OF THE RAS SIGNALING PATHWAY [J].
PUIL, L ;
LIU, JX ;
GISH, G ;
MBAMALU, G ;
BOWTELL, D ;
PELICCI, PG ;
ARLINGHAUS, R ;
PAWSON, T .
EMBO JOURNAL, 1994, 13 (04) :764-773
[30]  
REUTHER GW, UNPUB