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涉及人类染色体14q11上的T细胞受体Cδ基因座和染色体11p15转录区域的染色体易位t(11;14)的机制

The mechanism of chromosomal translocation t(11;14) involving the T-cell receptor C delta locus on human chromosome 14q11 and a transcribed region of chromosome 11p15.

作者信息

Boehm T, Baer R, Lavenir I, Forster A, Waters J J, Nacheva E, Rabbitts T H

机构信息

Medical Research Council, Addenbrooke's Hospital, Cambridge, UK.

出版信息

EMBO J. 1988 Feb;7(2):385-94. doi: 10.1002/j.1460-2075.1988.tb02825.x.

Abstract

A chromosomal translocation t(11;14) (p15;q11) is described in a human acute T-cell leukaemia of immature phenotype (CD3-, CD4-, CD8-). The translocation occurs at a T-cell receptor joining J delta segment, 12 kb upstream of the constant C delta gene and 98 kb upstream of the C alpha gene at chromosome band 14q11. Nucleotide sequencing shows that both J delta and C delta are very conserved between mouse and man. The region of chromosome 11 involved in the translocation is transcriptionally active and produces a 4-kb mRNA. The DNA sequence at the chromosome 11 junction shows a perfect match to a recombinase signal sequence implying that this translocation occurred by recombinase error. The occurrence of the translocation breakpoint at the C delta locus, normally rearranged in immature T cells, and the structure of the translocation junctions suggests that the translocation occurred during an attempt at normal rearrangement of the J delta segment in an early thymocyte.

摘要

在一例具有未成熟表型(CD3-、CD4-、CD8-)的人类急性T细胞白血病中,描述了一种染色体易位t(11;14) (p15;q11)。该易位发生在T细胞受体连接Jδ节段处,位于14号染色体带q11上恒定Cδ基因上游12 kb以及Cα基因上游98 kb处。核苷酸测序表明,Jδ和Cδ在小鼠和人类之间非常保守。参与易位的11号染色体区域具有转录活性,并产生一种4 kb的mRNA。11号染色体连接处的DNA序列与重组酶信号序列完全匹配,这意味着这种易位是由重组酶错误导致的。易位断点出现在通常在未成熟T细胞中重排的Cδ位点,以及易位连接点的结构表明,这种易位发生在早期胸腺细胞中Jδ节段正常重排的尝试过程中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b9f/454331/dce81ade1a31/emboj00139-0092-a.jpg

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