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对融合LCK和TCRB的T细胞急性淋巴细胞白血病相关t(1;7)(p34;q34)进行分子分析。

Molecular analysis of the T-cell acute lymphoblastic leukemia-associated t(1;7)(p34;q34) that fuses LCK and TCRB.

作者信息

Burnett R C, Thirman M J, Rowley J D, Diaz M O

机构信息

Department of Medicine, University of Chicago, IL.

出版信息

Blood. 1994 Aug 15;84(4):1232-6.

PMID:8049439
Abstract

Previously we had characterized the t(1;7)(p34;q34) translocation from HSB-2. This translocation fused the beta T-cell receptor gene (TCRB) constant region and transcriptional enhancer with the type I transcription unit of the LCK gene on the derivative 1 [der(1)] chromosome. The type II promoter was translocated to the der(7) chromosome. Regarding the mechanism of the t(1;7) in HSB-2, we identified an alternating purine-pyrimidine tract (G-T)17 at the 1p34/LCK breakpoint. Additionally, sequence analysis of both breakpoint junctions provided data that implicate the V(D)J recombinase in formation of the t(1;7). A heptamer-nonamer recognition sequence with a 12-bp spacer was found in the immediate vicinity of the 1p34/LCK breakpoint and, thus, chromosomal breakage at 1p34 may be explained as resulting from recombinase activity. Because phosphorylation of Tyr-505 in vivo regulates the tyrosine kinase activity of p56lck we amplified a region from LCK exon 12 that contains the codon for Tyr-505 and showed no mutation of this codon in HSB-2 DNA and, therefore, p56lck in HSB-2 is not activated by mutation of Tyr-505. We have analyzed LCK gene expression in HSB-2 and SUP-T12 cell lines. RNase protection analysis identified almost exclusively type I transcripts in HSB-2. An independent t(1;7) in SUP-T12 also resulted in the juxtaposition of LCK to TCRB. The breakpoint in SUP-T12 occurred 2 kb 5' of the type II promoter, leaving an intact LCK gene on the der(1) chromosome. RNase protection analysis identified both type I and type II LCK transcripts in a 3:1 ratio in SUP-T12. Factors other than proximity to the TCRB enhancer must affect promoter utilization in this cell line.

摘要

此前我们已对源自HSB-2细胞系的t(1;7)(p34;q34)易位进行了特征描述。该易位使β- T细胞受体基因(TCRB)恒定区和转录增强子与1号衍生染色体[der(1)]上LCK基因的I型转录单元融合。II型启动子易位至der(7)染色体。关于HSB-2细胞系中t(1;7)易位的机制,我们在1p34/LCK断点处鉴定出一个交替嘌呤-嘧啶序列(G-T)17。此外,对两个断点连接区的序列分析提供的数据表明V(D)J重组酶参与了t(1;7)的形成。在1p34/LCK断点紧邻区域发现了一个带有12bp间隔序列的七聚体-九聚体识别序列,因此,1p34处的染色体断裂可解释为由重组酶活性导致。由于体内Tyr-505的磷酸化调节p56lck的酪氨酸激酶活性,我们扩增了LCK外显子12中包含Tyr-505密码子的区域,结果显示HSB-2细胞系的DNA中该密码子无突变,因此,HSB-2细胞系中的p56lck并非因Tyr-505突变而被激活。我们分析了HSB-2和SUP-T12细胞系中LCK基因的表达情况。核糖核酸酶保护分析表明,HSB-2细胞系中几乎只存在I型转录本。SUP-T12细胞系中一个独立的t(1;7)易位也导致LCK与TCRB并列。SUP-T12细胞系中的断点位于II型启动子上游2kb处,der(1)染色体上的LCK基因保持完整。核糖核酸酶保护分析表明,SUP-T12细胞系中I型和II型LCK转录本的比例为3:1。除了与TCRB增强子的接近程度外,其他因素必定也影响了该细胞系中启动子的利用。

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