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可诱导细胞毒性T淋巴细胞相关基因转录本CTLA-1序列及该基因在小鼠14号染色体上的定位。

The inducible cytotoxic T-lymphocyte-associated gene transcript CTLA-1 sequence and gene localization to mouse chromosome 14.

作者信息

Brunet J F, Dosseto M, Denizot F, Mattei M G, Clark W R, Haqqi T M, Ferrier P, Nabholz M, Schmitt-Verhulst A M, Luciani M F, Golstein P

出版信息

Nature. 1986;322(6076):268-71. doi: 10.1038/322268a0.

Abstract

Classical phenomenological approaches to the study of the mechanism of T-cell-mediated cytotoxicity have now given way to a search for molecules involved in this function; this is attempted either by subcellular and biochemical fractionation of material from cytotoxic cells, or through the characterization of molecules recognized by cytotoxicity-inhibiting monoclonal antibodies Molecules having a role in cytotoxicity may also be identified by detecting the corresponding messenger RNA transcripts. Such an approach may include, as a first step, the search for transcripts as specific as possible to cytotoxic T cells; only secondarily can their actual relevance to cytotoxicity be investigated. We report here the preparation and systematic screening of a differential complementary DNA bank, in which we detected three distinct messenger RNA transcripts (CTLA-1, CTLA-2 and CTLA-3) present in various cytotoxic T cells but not (or less so) in a range of non-cytotoxic lymphoid cells. We describe the co-inducibility of these transcripts and of cytotoxicity in thymocytes and hybridoma cells, the sequence of CTLA-1 cDNA, its protein homology with serine esterases and the localization of the corresponding gene to mouse chromosome 14.

摘要

经典的现象学方法用于研究T细胞介导的细胞毒性机制,如今已让位于对参与此功能的分子的探索;这可以通过对细胞毒性细胞的物质进行亚细胞和生化分级分离来尝试,或者通过表征细胞毒性抑制单克隆抗体识别的分子来实现。在细胞毒性中起作用的分子也可以通过检测相应的信使RNA转录本来鉴定。这样的方法可能包括,作为第一步,寻找对细胞毒性T细胞尽可能特异的转录本;只有其次才能研究它们与细胞毒性的实际相关性。我们在此报告了一个差异互补DNA文库的制备和系统筛选,在其中我们检测到三种不同的信使RNA转录本(CTLA-1、CTLA-2和CTLA-3)存在于各种细胞毒性T细胞中,但在一系列非细胞毒性淋巴细胞中不存在(或较少存在)。我们描述了这些转录本与胸腺细胞和杂交瘤细胞中的细胞毒性的共同诱导性、CTLA-1 cDNA的序列、其与丝氨酸酯酶的蛋白质同源性以及相应基因在小鼠第14号染色体上的定位。

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