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对伴有染色体易位t(4;11)的急性淋巴细胞性SEM细胞系中的染色体断点和融合转录本进行分子分析。

Molecular analysis of the chromosomal breakpoint and fusion transcripts in the acute lymphoblastic SEM cell line with chromosomal translocation t(4;11).

作者信息

Marschalek R, Greil J, Löchner K, Nilson I, Siegler G, Zweckbronner I, Beck J D, Fey G H

机构信息

Department of Genetics, University of Erlangen-Nürnberg, Germany.

出版信息

Br J Haematol. 1995 Jun;90(2):308-20. doi: 10.1111/j.1365-2141.1995.tb05151.x.

Abstract

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.

摘要

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。

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