2 TANDEMLY ORGANIZED HUMAN GENES ENCODING THE T-CELL GAMMA CONSTANT-REGION SEQUENCES SHOW MULTIPLE REARRANGEMENT IN DIFFERENT T-CELL TYPES
2 TANDEMLY ORGANIZED HUMAN GENES ENCODING THE T-CELL GAMMA CONSTANT-REGION SEQUENCES SHOW MULTIPLE REARRANGEMENT IN DIFFERENT T-CELL TYPES
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DOI:
10.1038/316464a0
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发表时间:
1985-01-01
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:
LEFRANC, MP;RABBITTS, TH
The recent detailed analysis of genes that undergo rearrangement in T cells has shown that the T-cell receptor genes encodingαandβ-chains are involved in specific alterations in T-cell DNA analogous to the immunoglobulin genes1–9. A third type of gene, designatedγ, has been isolated from mouse cytotoxic T lymphocytes10, and evidence suggests that the mouse displays very limited diversity in this gene system11, having only three variable-region (V) genes and three constant-region (C) genes12. The function of the so-called T-cellγgene is unknown. We have isolated genomic genes encoding the human homologue of the mouse T-cellγgene; as there is no evidence that this T-cell rearranging gene is anything to do with the T3 molecule, we have designated the human T-cell rearranging gene as TRGγ(ref. 13), to avoid confusion with the T3γ-chain, and have shown that the gene locus maps to chromosome 7 in humans13. We now report that human DNA contains two tandemly arranged TRGγconstant-region genes about 16 kilobases apart. These two genes show multiple rearrangement patterns in a variety of T cells, including helper and cytotoxic/suppressor type, as well as in all forms of T-cell leukaemia. Our results indicate variability of this T-cell gene system in man compared with the analogous system in mouse.