ACUTE MIXED-LINEAGE LEUKEMIA T(4-11)(Q21-Q23) GENERATES AN MLL-AF4 FUSION PRODUCT

被引:228
作者
DOMER, PH
FAKHARZADEH, SS
CHEN, CS
JOCKEL, J
JOHANSEN, L
SILVERMAN, GA
KERSEY, JH
KORSMEYER, SJ
机构
[1] WASHINGTON UNIV,SCH MED,DEPT MED,ST LOUIS,MO 63110
[2] WASHINGTON UNIV,SCH MED,DEPT PATHOL,ST LOUIS,MO 63110
[3] UNIV MINNESOTA,CTR CANC,DEPT LAB MED,MINNEAPOLIS,MN 55455
[4] UNIV MINNESOTA,CTR CANC,DEPT PATHOL,MINNEAPOLIS,MN 55455
[5] UNIV MINNESOTA,CTR CANC,DEPT PEDIAT,MINNEAPOLIS,MN 55455
关键词
D O I
10.1073/pnas.90.16.7884
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
A chromosomal translocation, t(4;11)(q21;q23), is associated with an aggressive mixed-lineage leukemia. A yeast artificial chromosome was used to clone the chromosomal breakpoint of this translocation in the RS4;11 cell line. The breakpoint sequences revealed an inverted repeat bordered by a consensus site for topoisomerase II binding and cleavage as well as chi-like elements. The der(11) chromosome encodes a fusion RNA and predicted chimeric protein between the 11q23 gene MLL and a 4q21 gene designated AF4. The sequence of the complete open reading frame for this fusion transcript reveals the MLL protein to have homology with DNA methyltransferase, the Drosophila trithorax gene product, and the ''AT-hook'' motif of high-mobility-group proteins. An alternative splice that deletes the AT-hook region of MLL was identified. AF4 is a serine- and proline-rich putative transcription factor with a glutamine-rich carboxyl terminus. The composition of the complete MLL-AF4 fusion product argues that it may act through either a gain-of-function or a dominant negative mechanism in leukemogenesis.
引用
收藏
页码:7884 / 7888
页数:5
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