The t(11;16)(q23;p13) translocation in myelodysplastic syndrome fuses the MLL gene to the CBP gene

被引:193
作者
Taki, T
Sako, M
Tsuchida, M
Hayashi, Y
机构
[1] UNIV TOKYO, FAC MED, DEPT PEDIAT, BUNKYO KU, TOKYO 113, JAPAN
[2] HAMAMATSU UNIV SCH MED, DEPT PEDIAT, HAMAMATSU, SHIZUOKA 43131, JAPAN
[3] OSAKA CITY UNIV, GEN HOSP, DEPT PEDIAT, OSAKA 558, JAPAN
[4] IBARAKI CHILDRENS HOSP, DEPT INTERNAL MED, MITO, IBARAKI, JAPAN
关键词
D O I
10.1182/blood.V89.11.3945
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The recurrent translocation t(11;16)(q23;p13) has been reported to be associated with therapy-related acute leukemia. The MLL gene involved in other 11q23 abnormalities was also rearranged by this translocation. We analyzed two patients with myelodysplastic syndrome with t(11;16) and showed that the MLL gene on 11q23 was fused with CREB-binding protein (CBP) gene on 16p13 in these patients, The CBP gene encodes a transcriptional adaptor/coactivator protein and it is mutated in patients with Rubinstein-Taybi syndrome, The CBP gene is also involved in acute myeloid leukemia (AML) with t(8;16)(pll;p13), In-frame MLL-CBP fusion transcripts combine the MLL AT-hook motifs and DNA methyltransferase homology region with a largely intact CBP. Our results combined with the finding of the MOZ-CBP fusion in t(8; 16)-AML suggest that the CBP gene may be associated with leukemogenesis through translocations. (C) 1997 by The American Society of Hematology.
引用
收藏
页码:3945 / 3950
页数:6
相关论文
共 36 条
[1]   The translocation t(8;l6)(p11, p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB binding protein [J].
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 .
NATURE GENETICS, 1996, 14 (01) :33-41
[2]  
BUIJS A, 1995, ONCOGENE, V10, P1511
[3]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[4]   An MII-AF9 fusion gene made by homologous recombination causes acute leukemia in chimeric mice: A method to create fusion oncogenes [J].
Corral, J ;
Lavenir, I ;
Impey, H ;
Warren, AJ ;
Forster, A ;
Larson, TA ;
Bell, S ;
McKenzie, ANJ ;
King, G ;
Rabbitts, TH .
CELL, 1996, 85 (06) :853-861
[5]  
DJABALI M, 1992, NAT GENET, V2, P112
[6]   FUSION OF THE TEL GENE ON 12P13 TO THE AML1 GENE ON 21Q22 IN ACUTE LYMPHOBLASTIC-LEUKEMIA [J].
GOLUB, TR ;
BARKER, GF ;
BOHLANDER, SK ;
HIEBERT, SW ;
WARD, DC ;
BRAYWARD, P ;
MORGAN, E ;
RAIMONDI, SC ;
ROWLEY, JD ;
GILLILAND, DG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (11) :4917-4921
[7]   THE T(4-11) CHROMOSOME-TRANSLOCATION OF HUMAN ACUTE LEUKEMIAS FUSES THE ALL-1 GENE, RELATED TO DROSOPHILA-TRITHORAX, TO THE AF-4 GENE [J].
GU, Y ;
NAKAMURA, T ;
ALDER, H ;
PRASAD, R ;
CANAANI, O ;
CIMINO, G ;
CROCE, CM ;
CANAANI, E .
CELL, 1992, 71 (04) :701-708
[8]  
HUNGER SP, 1993, BLOOD, V81, P3197
[9]   MUTATIONS OF THE P53 AND RAS GENES IN CHILDHOOD T(1-19)-ACUTE LYMPHOBLASTIC-LEUKEMIA [J].
KAWAMURA, M ;
KIKUCHI, A ;
KOBAYASHI, S ;
HANADA, R ;
YAMAMOTO, K ;
HORIBE, K ;
SHIKANO, T ;
UEDA, K ;
HAYASHI, K ;
SEKIYA, T ;
HAYASHI, Y .
BLOOD, 1995, 85 (09) :2546-2552
[10]   Identification of AF-6 and canoe as putative targets for Ras [J].
Kuriyama, M ;
Harada, N ;
Kuroda, S ;
Yamamoto, T ;
Nakafuku, M ;
Iwamatsu, A ;
Yamamoto, D ;
Prasad, R ;
Croce, C ;
Canaani, E ;
Kaibuchi, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (02) :607-610