INVOLVEMENT OF A HOMOLOG OF DROSOPHILA-TRITHORAX BY 11Q23 CHROMOSOMAL TRANSLOCATIONS IN ACUTE LEUKEMIAS

被引:894
作者
TKACHUK, DC
KOHLER, S
CLEARY, ML
机构
[1] Laboratory of Experimental Oncology Department, Pathology Stanford University School of Medicine Stanford
关键词
D O I
10.1016/0092-8674(92)90602-9
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
We have identified a human homolog of the Drosophila trithorax protein that is structurally altered by 11q23 translocations in acute leukemias. Human trithorax (HRX) is a predicted 431 kd protein containing two potential DNA-binding motifs consisting of zinc fingers conserved with the fly protein and nonconserved amino-terminal "AT hook" motifs related to the DNA-binding motifs in HMG proteins. 11q23 translocations disrupt the HRX gene between these two motifs, and in a t(11;19)-carrying cell line fusion transcripts are expressed from both derivative chromosomes. The more abundant derivative 11 transcript codes for a chimeric protein containing the AT hook motifs fused to a previously undescribed protein (ENL) from chromosome 19. These data suggest a novel role for a trithorax-homologous protein in multilineage human leukemias that may be mediated by DNA binding within the minor groove at AT-rich sites, implicated to play an important role in bacterial IHF-, yeast datin-, and mammalian HMG-mediated gene activation.
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页码:691 / 700
页数:10
相关论文
共 46 条
[1]  
ASHLEY CT, 1989, J BIOL CHEM, V264, P8394
[2]   PROSITE - A DICTIONARY OF SITES AND PATTERNS IN PROTEINS [J].
BAIROCH, A .
NUCLEIC ACIDS RESEARCH, 1991, 19 :2241-2245
[3]   INTERACTIONS OF POLYCOMB AND TRITHORAX WITH CIS REGULATORY REGIONS OF ULTRABITHORAX DURING THE DEVELOPMENT OF DROSOPHILA-MELANOGASTER [J].
CASTELLIGAIR, JE ;
GARCIABELLIDO, A .
EMBO JOURNAL, 1990, 9 (13) :4267-4275
[4]  
CHEN CS, 1991, BLOOD, V78, P2498
[5]   SPKK MOTIFS PREFER TO BIND TO DNA AT A/T-RICH SITES [J].
CHURCHILL, MEA ;
SUZUKI, M .
EMBO JOURNAL, 1989, 8 (13) :4189-4195
[6]  
CIMINO G, 1992, CANCER RES, V52, P3811
[7]  
CIMINO G, 1991, CANCER RES, V51, P6712
[8]   CLONING AND STRUCTURAL-ANALYSIS OF CDNAS FOR BCL-2 AND A HYBRID BCL-2/IMMUNOGLOBULIN TRANSCRIPT RESULTING FROM THE T(14-18) TRANSLOCATION [J].
CLEARY, ML ;
SMITH, SD ;
SKLAR, J .
CELL, 1986, 47 (01) :19-28
[9]   ONCOGENIC CONVERSION OF TRANSCRIPTION FACTORS BY CHROMOSOMAL TRANSLOCATIONS [J].
CLEARY, ML .
CELL, 1991, 66 (04) :619-622
[10]   CD3G IS WITHIN 200 KB OF THE LEUKEMIC T(4,II) TRANSLOCATION BREAKPOINT [J].
DAS, S ;
COTTER, FE ;
GIBBONS, B ;
DHUT, S ;
YOUNG, BD .
GENES CHROMOSOMES & CANCER, 1991, 3 (01) :44-47