COMPLEXITY OF HUMAN T-CELL ANTIGEN RECEPTOR BETA-CHAIN CONSTANT-REGION AND VARIABLE-REGION GENES
COMPLEXITY OF HUMAN T-CELL ANTIGEN RECEPTOR BETA-CHAIN CONSTANT-REGION AND VARIABLE-REGION GENES
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DOI:
10.1038/312541a0
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发表时间:
1984-01-01
期刊:
影响因子:
64.8
通讯作者:
RABBITTS, TH
中科院分区:
文献类型:
--
作者:
SIMS, JE;TUNNACLIFFE, A;RABBITTS, TH
Immune systems of vertebrates function via two types of effector cells, B and T cells, which are capable of antigen-specific recognition. The immunoglobulins, which serve as antigen receptors on B cells, have been well characterized with respect to gene structure1, unlike the T-cell receptors. Recently, cDNA clones thought to correspond to theβ-chain locus2–4of the human and mouse T-cell receptor have been described. The presumptiveβ-chain clones detect gene rearrangement specifically in T-cell DNA and show homology with immunoglobulin light chains. The similarity of the T-cellβ-chain gene system to the immunoglobulin genes has been further demonstrated by the recent observation of variable- and constant-region gene segments as well as joining segments and putative diversity segments5,6. We report here the characterization of cDNA and genomic clones encoding human T-cell receptorβ-chain genes. There are two constant-region genes (Cβ1 andCβ2), each capable of rearrangement and expression as RNA. The gene arrangement, analogous to that of mouseβ-chain genes6–8, shows strong evolutionary conservation of the dualCβgene system in these two species.