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Thymocyte circular DNA excised from T cell receptor alpha‐delta gene complex.
Author(s) -
Okazaki K.,
Sakano H.
Publication year - 1988
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1002/j.1460-2075.1988.tb02994.x
Subject(s) - biology , thymocyte , gene , alpha (finance) , dna , delta , microbiology and biotechnology , genetics , t cell receptor , cd8 , t cell , immune system , medicine , construct validity , nursing , engineering , patient satisfaction , aerospace engineering
We have characterized thymocyte circular DNA excised from the T cell receptor alpha‐delta gene complex. Some delta gene clones contained unusual recombinant structures derived from V‐(D)‐J joining: (i) a reciprocal joint of direct V to J delta joining, skipping the D delta segment; (ii) a V‐D delta coding joint lacking an adjacent D delta‐J delta coding joint; (iii) a V‐ D structure containing two D delta segments. Many of the alpha gen clones contained both coding and reciprocal joints of V alpha‐to‐J alpha joining on the same structure. Most of these coding joints were out of phase; however, in one clone there was an in‐phase V‐J alpha structure. Interestingly, some alpha gene clones contained the same V gene sequence as rearranged in the delta gene clone, indicating that the same V gene family, at least in part, could be utilized for both the alpha and delta gene systems.

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