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一个突变的内含子序列编码一种抗原肽,该抗原肽可被人黑色素瘤上的细胞毒性T淋巴细胞识别。

A mutated intron sequence codes for an antigenic peptide recognized by cytolytic T lymphocytes on a human melanoma.

作者信息

Coulie P G, Lehmann F, Lethé B, Herman J, Lurquin C, Andrawiss M, Boon T

机构信息

Ludwig Institute for Cancer Research, UCL 7459, Brussels, Belgium.

出版信息

Proc Natl Acad Sci U S A. 1995 Aug 15;92(17):7976-80. doi: 10.1073/pnas.92.17.7976.

Abstract

We have identified an antigen recognized on a human melanoma by autologous cytolytic T lymphocytes. It is encoded by a gene that is expressed in many normal tissues. Remarkably, the sequence coding for the antigenic peptide is located across an exon-intron junction. A point mutation is present in the intron that generates an amino acid change that is essential for the recognition of the peptide by the anti-tumor cytotoxic T lymphocytes. This observation suggests that the T-cell-mediated surveillance of the integrity of the genome may extend to some intronic regions.

摘要

我们已经鉴定出一种可被自体溶细胞性T淋巴细胞识别的人类黑色素瘤抗原。它由一个在许多正常组织中表达的基因编码。值得注意的是,编码抗原肽的序列位于一个外显子-内含子交界处。内含子中存在一个点突变,该突变导致氨基酸改变,这对于抗肿瘤细胞毒性T淋巴细胞识别该肽至关重要。这一观察结果表明,T细胞介导的基因组完整性监测可能延伸到一些内含子区域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e4e/41269/5554013867e8/pnas01495-0382-a.jpg

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