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人类δT细胞受体:重排、缺失与易位。

Human delta T cell receptor: rearrangement, deletion, and translocation.

作者信息

Korsmeyer S J, Hockett R D, McGuire E A, Nunez G

机构信息

Department of Medicine, Howard Hughes Medical Institute, Washington University School of Medicine, St. Louis, Missouri 63110.

出版信息

Princess Takamatsu Symp. 1988;19:137-45.

PMID:2978616
Abstract

Individual T cells express the CD3 molecule in association with alternative gamma delta or alpha beta heterodimeric T cell receptors (TCR). The delta TCR, used in one type of T cell is located within the alpha TCR gene used in quite another cell. T cell precursors and occasional gamma delta T cells in humans possess an unexpected 2.0 Kb mRNA in which a tandemly repeated motif, T early alpha (TEA), has been spliced to the constant (C alpha) region. Long range pulse field gel mapping as well as molecular cloning reveal that TEA is located immediately 5' to the most upstream joining (J alpha) segments of the alpha TCR locus. The human delta TCR locus is immediately 5' to TEA and diversity (D delta 1 +2), J delta 1 +2, C delta, and TEA are linked within 35 Kb. The human delta TCR locus conserves a 12/23 bp spacer paradigm and D delta 1 and D delta 2 are frequently recombined as D delta 1/D delta 2, and reveal exonucleolytic trimming with extensive "N" segment addition. Thus, despite the predominant use of one V delta and J delta segment considerable delta diversity is generated. T cell acute lymphoblastic leukemias (ALL) represent clonal expansions of maturationally arrested cells at specific stages of thymic ontogeny. The gamma delta T-ALLs display allelic exclusion for the delta TCR. Moreover, pre T cells within this group indicate that delta TCR rearrangement can occur prior to the activation of gamma, beta, and alpha loci.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

单个T细胞表达与替代性γδ或αβ异二聚体T细胞受体(TCR)相关联的CD3分子。一种T细胞中使用的δTCR位于另一种细胞中使用的αTCR基因内。人类的T细胞前体和偶尔的γδT细胞拥有一种意想不到的2.0 Kb mRNA,其中一个串联重复基序,即T早期α(TEA),已剪接到恒定(Cα)区域。长距离脉冲场凝胶图谱分析以及分子克隆表明TEA位于αTCR基因座最上游连接(Jα)片段的紧邻5'端。人类δTCR基因座紧邻TEA的5'端,并且多样性(Dδ1 +2)、Jδ1 +2、Cδ和TEA在35 Kb范围内相连。人类δTCR基因座保留了12/23 bp间隔模式,Dδ1和Dδ2经常作为Dδ1/Dδ2进行重组,并显示出广泛添加“N”片段的外切核酸酶修剪。因此,尽管主要使用一个Vδ和Jδ片段,但仍产生了相当大的δ多样性。T细胞急性淋巴细胞白血病(ALL)代表胸腺发育特定阶段成熟停滞细胞的克隆性扩增。γδT-ALL对δTCR表现出等位基因排斥。此外,该组中的前T细胞表明δTCR重排可在γ、β和α基因座激活之前发生。(摘要截断于250字)

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