RT-PCR DIAGNOSIS OF PATIENTS WITH ACUTE NONLYMPHOCYTIC LEUKEMIA AND INV(16)(P13Q22) AND IDENTIFICATION OF NEW ALTERNATIVE SPLICING IN CBFB-MYH11 TRANSCRIPTS

被引:56
作者
VANDERREIJDEN, BA
LOMBARDO, M
DAUWERSE, HG
GILES, RH
MUHLEMATTER, D
BELLOMO, MJ
WESSELS, HW
BEVERSTOCK, GC
VANOMMEN, GJB
HAGEMEIJER, A
BREUNING, MH
机构
[1] LEIDEN UNIV,SYLVIUS LABS,DEPT HUMAN GENET,2333 AL LEIDEN,NETHERLANDS
[2] ERASMUS UNIV ROTTERDAM,DEPT CELL BIOL & GENET,3000 DR ROTTERDAM,NETHERLANDS
[3] CHU VAUDOIS,DIV AUTONOME GENET MED,CH-1011 LAUSANNE,SWITZERLAND
关键词
D O I
10.1182/blood.V86.1.277.bloodjournal861277
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
As acute nonlymphocytic leukemia (ANLL) with inv(16) (p13q22) or t(16; 16)(p13; q22) has been shown to result from the fusion of transcription factor subunit core binding factor (CBFB) to a myosin heavy chain (MYH11), we sought to design methods to detect this rearrangement using reverse transcriptase-polymerase chain reaction (RT-PCR). In all of 27 inv(16)(p13q22) and four t(16;16)(p13;q22) cases tested, a chimeric CBFB-MYH11 transcript coding for an in-frame fusion protein was detected. In a more extensive RT-PCR analysis with different primer pairs, we detected a second new chimeric CBFB-MYH11 transcript in 10 of 11 patients tested. The CBFB-MYH11 reading frame of the second transcript was maintained in one patient but not in the others. We show that the different CBFB-MYH11 transcripts in one patient arise from alternative splicing. Translation of the transcript in which the CBFB-MYH11 reading frame is not maintained leads to a slightly truncated CBFB protein. (C) 1995 by The American Society of Hematology.
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页码:277 / 282
页数:6
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