The translocation t(8;l6)(p11, p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB binding protein

被引:645
作者
Borrow, J
Stanton, VP
Andresen, JM
Becher, R
Behm, FG
Chaganti, RSK
Civin, CI
Disteche, C
Dube, I
Frischauf, AM
Horsman, D
Mitelman, F
Volinia, S
Watmore, AE
Housman, DE
机构
[1] W GERMAN CANC CTR, D-45122 ESSEN 1, GERMANY
[2] ST JUDE CHILDRENS RES HOSP, MEMPHIS, TN 38101 USA
[3] MEM SLOAN KETTERING CANC CTR, NEW YORK, NY 10021 USA
[4] JOHNS HOPKINS ONCOL CTR, BALTIMORE, MD 21287 USA
[5] UNIV WASHINGTON, MED CTR, SEATTLE, WA 98195 USA
[6] UNIV TORONTO, SUNNYBROOK HLTH SCI CTR, TORONTO, ON M4N 3M5, CANADA
[7] IMPERIAL CANC RES FUND, LONDON WC2A 3PX, ENGLAND
[8] BRITISH COLUMBIA CANC AGCY, VANCOUVER, BC V5Z 4E6, CANADA
[9] UNIV LUND HOSP, DEPT CLIN GENET, S-22185 LUND, SWEDEN
[10] UNIV FERRARA, I-44100 FERRARA, ITALY
[11] CTR HUMAN GENET, SHEFFIELD S10 5DN, S YORKSHIRE, ENGLAND
关键词
D O I
10.1038/ng0996-33
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The recurrent translocation t(8;16)(p11;p13) is a cytogenetic hallmark for the M4/M5 subtype of acute myeloid leukaemia. Here we identify the breakpoint-associated genes. Positional cloning on chromosome 16 implicates the CREB-binding protein (CBP), a transcriptional adaptor/coactivator protein. At the chromosome 8 breakpoint we identify a novel gene, MOZ, which encodes a 2,004-amino-acid protein characterized by two C4HC3 zinc fingers and a single C2HC zinc finger in conjunction with a putative acetyltransferase signature. In-frame MOZ-CBP fusion transcripts combine the MOZ finger motifs and putative acetyltransferase domain with a largely intact CBP. We suggest that MOZ may represent a chromatin-associated acetyltransferase, and raise the possibility that a dominant MOZ-CBP fusion protein could mediate leukaemogenesis via aberrant chromatin acetylation.
引用
收藏
页码:33 / 41
页数:9
相关论文
共 59 条
[1]   THE PHD FINGER - IMPLICATIONS FOR CHROMATIN-MEDIATED TRANSCRIPTIONAL REGULATION [J].
AASLAND, R ;
GIBSON, TJ ;
STEWART, AF .
TRENDS IN BIOCHEMICAL SCIENCES, 1995, 20 (02) :56-59
[2]   XFIN - AN EMBRYONIC GENE ENCODING A MULTIFINGERED PROTEIN IN XENOPUS [J].
ALTABA, AR ;
PERRYOKEEFE, H ;
MELTON, DA .
EMBO JOURNAL, 1987, 6 (10) :3065-3070
[3]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[4]  
[Anonymous], 1988, CANCER GENET CYTOGEN, V30, P1
[5]   MODIFIERS OF POSITION EFFECT ARE SHARED BETWEEN TELOMERIC AND SILENT MATING-TYPE LOCI IN SACCHAROMYCES-CEREVISIAE [J].
APARICIO, OM ;
BILLINGTON, BL ;
GOTTSCHLING, DE .
CELL, 1991, 66 (06) :1279-1287
[6]   A FAMILY OF TRANSCRIPTIONAL ADAPTER PROTEINS TARGETED BY THE E1A ONCOPROTEIN [J].
ARANY, Z ;
NEWSOME, D ;
OLDREAD, E ;
LIVINGSTON, DM ;
ECKNER, R .
NATURE, 1995, 374 (6517) :81-84
[7]   ACTIVATION OF CAMP AND MITOGEN RESPONSIVE GENES RELIES ON A COMMON NUCLEAR FACTOR [J].
ARIAS, J ;
ALBERTS, AS ;
BRINDLE, P ;
CLARET, FX ;
SMEAL, T ;
KARIN, M ;
FERAMISCO, J ;
MONTMINY, M .
NATURE, 1994, 370 (6486) :226-229
[8]   TRANSCRIPTS OF THE DROSOPHILA BLASTODERM-SPECIFIC LOCUS, TERMINUS, ARE CONCENTRATED POSTERIORLY AND ENCODE A POTENTIAL DNA-BINDING FINGER [J].
BALDARELLI, RM ;
MAHONEY, PA ;
SALAS, F ;
GUSTAVSON, E ;
BOYER, PD ;
CHANG, MF ;
ROARK, M ;
LENGYEL, JA .
DEVELOPMENTAL BIOLOGY, 1988, 125 (01) :85-95
[9]   T(8 9)(P11 Q32) IN ATYPICAL CHRONIC MYELOID-LEUKEMIA - A NEW CYTOGENETIC-CLINICOPATHOLOGICAL ASSOCIATION [J].
BELLOMO, MJ ;
MUHLEMATTER, D ;
WICHT, M ;
DELACRETAZ, F ;
SCHMIDT, PM .
BRITISH JOURNAL OF HAEMATOLOGY, 1992, 81 (02) :307-308
[10]   TRANSCRIPTIONAL SILENCING IN YEAST IS ASSOCIATED WITH REDUCED NUCLEOSOME ACETYLATION [J].
BRAUNSTEIN, M ;
ROSE, AB ;
HOLMES, SG ;
ALLIS, CD ;
BROACH, JR .
GENES & DEVELOPMENT, 1993, 7 (04) :592-604