Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.


Science 7 June 1985:
Vol. 228. no. 4704, pp. 1204 - 1206
DOI: 10.1126/science.3839095

Articles

Science, Vol 228, Issue 4704, 1204-1206
Copyright © 1985 by American Association for the Advancement of Science


articles

A novel mechanism of somatic rearrangement predicted by a human T-cell antigen receptor beta-chain complementary DNA

AD Duby, KA Klein, C Murre, and JG Seidman

The T-cell antigen receptor is a cell surface molecule vital in mediating the cellular immune response. The arrangement and rearrangement of the gene segments encoding the beta-chain polypeptide of the receptor are similar to those of immunoglobulin gene segments. The two constant region genes of the human T-cell antigen receptor are 8 kilobases apart with a cluster of joining segments located 5' of each constant region gene. Although most beta-chain gene rearrangements involve the variable, diversity, and joining segments, analysis of a beta-chain complementary DNA clone suggests the occasional occurrence of another type of rearrangement.





To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)