Dialynas D P, Murre C, Quertermous T, Boss J M, Leiden J M, Seidman J G, Strominger J L
Proc Natl Acad Sci U S A. 1986 Apr;83(8):2619-23. doi: 10.1073/pnas.83.8.2619.
Complementary DNA (cDNA) encoding a human T-cell gamma chain has been cloned and sequenced. At the junction of the variable and joining regions, there is an apparent deletion of two nucleotides in the human cDNA sequence relative to the murine gamma-chain cDNA sequence, resulting simultaneously in the generation of an in-frame stop codon and in a translational frameshift. For this reason, the sequence presented here encodes an aberrantly rearranged human T-cell gamma chain. There are several surprising differences between the deduced human and murine gamma-chain amino acid sequences. These include poor homology in the variable region, poor homology in a discrete segment of the constant region precisely bounded by the expected junctions of exon CII, and the presence in the human sequence of five potential sites for N-linked glycosylation.
编码人T细胞γ链的互补DNA(cDNA)已被克隆和测序。在可变区和连接区的交界处,相对于鼠γ链cDNA序列,人cDNA序列中明显缺失了两个核苷酸,这同时导致了框内终止密码子的产生和翻译移码。因此,这里呈现的序列编码了一条异常重排的人T细胞γ链。推导的人γ链和鼠γ链氨基酸序列之间存在几个惊人的差异。这些差异包括可变区的同源性较差、恒定区一个离散片段的同源性较差,该片段正好由外显子CII的预期连接界定,以及人序列中存在五个潜在的N-糖基化位点。