A T cell clone with three potential TCR alpha chain rearrangements expresses only one receptor combination at the cell surface
Date
1996
Authors
Hayball, J.
Jones, C.
Lamb, J.
Lake, R.
Editors
Advisors
Journal Title
Journal ISSN
Volume Title
Type:
Journal article
Citation
Molecular Immunology, 1996; 33(15):1177-1181
Statement of Responsibility
John D. Hayball, Claerwen M. Jones, Jonathan R. Lamb and Richard A. Lake
Conference Name
Abstract
In determining the T cell receptor (TcR) usage of various T cell clones that recognize peptide antigens derived from allergens, a particular clone (AC20) was found, that apparently expressed three different species of mRNA encoding alpha chains. The logical conclusion that the cells were not clonal was refuted by the finding of only a single beta chain rearrangement. One of the alpha chains (V alpha20), was not in frame, but two V alpha8 transcripts of different lengths were both potentially translatable. Sequence analysis suggested that the shorter transcript was generated by a secondary splice event from the longer, through the use of a splice donor sequence encoded by the J alpha38 gene segment. The efficiency of excision of the intervening sequence is such that approximately equal amounts of the long and short transcripts occur in the steady state pool of mRNA. This phenomenon has been reported previously in TcR alpha rearrangements, but it has never been made clear whether these truncated chains can form a functional TcR. Reconstitution of a TcR negative cell line with these transcripts showed that only the full length alpha chain was able to pair efficiently with the beta chain to generate a functional receptor at the cell surface.
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Provenance
Journal formerly known as Immunochemistry
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Rights
© 1997 Published by Elsevier Science Ltd.