Marschalek R, Greil J, Löchner K, Nilson I, Siegler G, Zweckbronner I, Beck J D, Fey G H
Department of Genetics, University of Erlangen-Nürnberg, Germany.
Br J Haematol. 1995 Jun;90(2):308-20. doi: 10.1111/j.1365-2141.1995.tb05151.x.
The chromosomal breakpoint and fusion transcripts of the pre-B-leukaemia-derived SEM cell line carrying a reciprocal t(4;11)(q21;q23) translocation were analysed. The breakpoint from derivative chromosome der4 was cloned and sequenced. The crossover site was localized in intron 7 of the ALL-1 gene on chromosome 11q23 and in a large intron of the AF-4 (FEL) gene. RNA transcripts from both wild-type genes and both hybrid genes were detected by reverse transcriptase polymerase chain reaction (RT-PCR) assays. In addition, alternatively spliced mRNA species derived from the der4 chromosome were found. They were generated by using the exon 5' of the breakpoint on der4 as a common splice donor site and the 5' boundaries of exons 8 or 9 of the ALL-1 gene as alternative splice acceptor sites. The hypothesis is proposed that selective pressure operators to maintain the presence of both derivative chromosomes as important elements in the leukaemogenic process.
对携带相互易位t(4;11)(q21;q23)的前B淋巴细胞白血病来源的SEM细胞系的染色体断点和融合转录本进行了分析。对衍生染色体der4的断点进行了克隆和测序。交叉位点定位于11q23染色体上ALL-1基因的内含子7以及AF-4(FEL)基因的一个大内含子中。通过逆转录聚合酶链反应(RT-PCR)检测野生型基因和两种杂交基因的RNA转录本。此外,还发现了源自der4染色体的可变剪接mRNA种类。它们是通过将der4上断点的外显子5′用作共同剪接受体位点,并将ALL-1基因外显子8或9的5′边界用作可变剪接供体位点而产生的。提出了这样的假说:选择性压力作用因子维持两条衍生染色体的存在,作为白血病发生过程中的重要因素。