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
论文数: 0引用数: 0
h-index: 0
机构:LEIDEN UNIV,SYLVIUS LABS,DEPT HUMAN GENET,2333 AL LEIDEN,NETHERLANDS
VANDERREIJDEN, BA
LOMBARDO, M
论文数: 0引用数: 0
h-index: 0
机构:LEIDEN UNIV,SYLVIUS LABS,DEPT HUMAN GENET,2333 AL LEIDEN,NETHERLANDS
LOMBARDO, M
DAUWERSE, HG
论文数: 0引用数: 0
h-index: 0
机构:LEIDEN UNIV,SYLVIUS LABS,DEPT HUMAN GENET,2333 AL LEIDEN,NETHERLANDS
DAUWERSE, HG
GILES, RH
论文数: 0引用数: 0
h-index: 0
机构:LEIDEN UNIV,SYLVIUS LABS,DEPT HUMAN GENET,2333 AL LEIDEN,NETHERLANDS
GILES, RH
MUHLEMATTER, D
论文数: 0引用数: 0
h-index: 0
机构:LEIDEN UNIV,SYLVIUS LABS,DEPT HUMAN GENET,2333 AL LEIDEN,NETHERLANDS
MUHLEMATTER, D
BELLOMO, MJ
论文数: 0引用数: 0
h-index: 0
机构:LEIDEN UNIV,SYLVIUS LABS,DEPT HUMAN GENET,2333 AL LEIDEN,NETHERLANDS
BELLOMO, MJ
WESSELS, HW
论文数: 0引用数: 0
h-index: 0
机构:LEIDEN UNIV,SYLVIUS LABS,DEPT HUMAN GENET,2333 AL LEIDEN,NETHERLANDS
WESSELS, HW
BEVERSTOCK, GC
论文数: 0引用数: 0
h-index: 0
机构:LEIDEN UNIV,SYLVIUS LABS,DEPT HUMAN GENET,2333 AL LEIDEN,NETHERLANDS
BEVERSTOCK, GC
VANOMMEN, GJB
论文数: 0引用数: 0
h-index: 0
机构:LEIDEN UNIV,SYLVIUS LABS,DEPT HUMAN GENET,2333 AL LEIDEN,NETHERLANDS
VANOMMEN, GJB
HAGEMEIJER, A
论文数: 0引用数: 0
h-index: 0
机构:LEIDEN UNIV,SYLVIUS LABS,DEPT HUMAN GENET,2333 AL LEIDEN,NETHERLANDS
HAGEMEIJER, A
BREUNING, MH
论文数: 0引用数: 0
h-index: 0
机构:LEIDEN UNIV,SYLVIUS LABS,DEPT HUMAN GENET,2333 AL LEIDEN,NETHERLANDS
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
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.