Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/11657
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Type: Journal article
Title: A T cell clone with three potential TCR alpha chain rearrangements expresses only one receptor combination at the cell surface
Author: Hayball, J.
Jones, C.
Lamb, J.
Lake, R.
Citation: Molecular Immunology, 1996; 33(15):1177-1181
Publisher: Elsevier Science
Issue Date: 1996
ISSN: 0161-5890
1872-9142
Statement of
Responsibility: 
John D. Hayball, Claerwen M. Jones, Jonathan R. Lamb and Richard A. Lake
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.
Keywords: T cell receptor; alternative splice variants
Provenance: Journal formerly known as Immunochemistry
Rights: © 1997 Published by Elsevier Science Ltd.
DOI: 10.1016/S0161-5890(96)00076-4
Published version: http://dx.doi.org/10.1016/s0161-5890(96)00076-4
Appears in Collections:Aurora harvest 7
Microbiology and Immunology publications

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