Chien Y, Becker D M, Lindsten T, Okamura M, Cohen D I, Davis M M
Nature. 1984;312(5989):31-5. doi: 10.1038/312031a0.
By subtractive cDNA hybridizations, we have isolated a new species of T-cell receptor cDNA clone whose predicted amino acid sequence has homology to variable, constant, joining and diversity segments of immunoglobulins and T-cell receptors. The corresponding genomic sequence is also rearranged in several T-cell DNAs. The four potential N-linked glycosylation sites, frequency of expression and predicted molecular weight (27,800) of this molecule make it a likely candidate for the alpha-chain of the T-cell receptor. Expression data also indicate that this gene may be activated at a later stage of T-cell differentiation than the beta-chain.
通过消减cDNA杂交技术,我们分离出了一种新的T细胞受体cDNA克隆,其预测的氨基酸序列与免疫球蛋白和T细胞受体的可变区、恒定区、连接区和多样性区段具有同源性。相应的基因组序列在几种T细胞DNA中也发生了重排。该分子的四个潜在N-糖基化位点、表达频率和预测分子量(27,800)使其成为T细胞受体α链的一个可能候选者。表达数据还表明,该基因可能在T细胞分化的后期比β链被激活。