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编码人类T细胞受体δ亚基的基因克隆揭示了其在α亚基基因座内的物理组织及其在T细胞恶性肿瘤染色体易位中的作用。

Cloning of the gene encoding the delta subunit of the human T-cell receptor reveals its physical organization within the alpha-subunit locus and its involvement in chromosome translocations in T-cell malignancy.

作者信息

Isobe M, Russo G, Haluska F G, Croce C M

机构信息

Wistar Institute of Anatomy and Biology, Philadelphia, PA 19104.

出版信息

Proc Natl Acad Sci U S A. 1988 Jun;85(11):3933-7. doi: 10.1073/pnas.85.11.3933.

Abstract

By taking advantage of "chromosomal walking" techniques, we have obtained clones that encompass the T-cell receptor (TCR) delta-chain gene. We analyzed clones spanning the entire J alpha region extending 115 kilobases 5' of the TCR alpha-chain constant region and have shown that the TCR delta-chain gene is located over 80 kilobases 5' of C alpha. TCR delta-chain gene is rearranged in the gamma/delta-expressing T-cell line Peer and is deleted in alpha/beta-expressing T-cell lines. Sequence analysis of portions of this genomic region demonstrates its identity with previously described cDNA clones corresponding to the C delta and J delta segments. Furthermore, we have analyzed a t(8;14)-(q24;q11) chromosome translocation from a T-cell leukemia and have shown that the J delta segment is rearranged in cells deriving from this tumor and probably directly involved in the translocation. Thus, the newly cloned TCR delta chain is implicated in the genesis of chromosome translocations in T-cell malignancies carrying cytogenetic abnormalities of band 14q11.

摘要

通过利用“染色体步移”技术,我们获得了包含T细胞受体(TCR)δ链基因的克隆。我们分析了跨越整个Jα区域的克隆,该区域延伸至TCRα链恒定区5'端115千碱基处,并表明TCRδ链基因位于Cα基因5'端超过80千碱基处。TCRδ链基因在表达γ/δ的T细胞系Peer中发生重排,而在表达α/β的T细胞系中缺失。对该基因组区域部分片段的序列分析表明,它与先前描述的对应于Cδ和Jδ区段的cDNA克隆相同。此外,我们分析了一例T细胞白血病的t(8;14)-(q24;q11)染色体易位,结果表明Jδ区段在源自该肿瘤的细胞中发生重排,并且可能直接参与了易位过程。因此,新克隆的TCRδ链与携带14q11带细胞遗传学异常的T细胞恶性肿瘤中染色体易位的发生有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0094/280334/9f6bd7a49bc1/pnas00263-0283-a.jpg

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