The contribution of template-independent nucleotide addition to antigen receptor diversity is unknown. We therefore determined the size of the T cell receptor (TCR)α/β repertoire in mice bearing a null mutation on both alleles of the terminal deoxynucleotidyl transferase (Tdt) gene. We used a method based upon polymerase chain reaction amplification and exhaustive sequencing of various AV-AJ and BV-BJ combinations. In both wild-type and Tdt°/° mice, TCRAV diversity is one order of magnitude lower than the TCRBV diversity. In Tdt°/° animals, TCRBV chain diversity is reduced 10-fold compared with wild-type mice. In addition, in Tdt°/° mice, one BV chain can associate with three to four AV chains as in wild-type mice. The α/β repertoire size in Tdt°/° mice is estimated to be 105 distinct receptors, ∼5–10% of that calculated for wild-type mice. Thus, while Tdt activity is not involved in the combinatorial diversity resulting from α/β pairing, it contributes to at least 90% of TCRα/β diversity.
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5 November 2001
Brief Definitive Report|
November 05 2001
Most α/β T Cell Receptor Diversity Is Due to Terminal Deoxynucleotidyl Transferase
Jean-Pierre Cabaniols,
Jean-Pierre Cabaniols
Unité de Biologie Moléculaire du Gène, Institut National de la Sante et de la Recherche Medicale U277, Institut Pasteur, 75 724 Paris, France
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Nicolas Fazilleau,
Nicolas Fazilleau
Unité de Biologie Moléculaire du Gène, Institut National de la Sante et de la Recherche Medicale U277, Institut Pasteur, 75 724 Paris, France
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Armanda Casrouge,
Armanda Casrouge
Unité de Biologie Moléculaire du Gène, Institut National de la Sante et de la Recherche Medicale U277, Institut Pasteur, 75 724 Paris, France
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Philippe Kourilsky,
Philippe Kourilsky
Unité de Biologie Moléculaire du Gène, Institut National de la Sante et de la Recherche Medicale U277, Institut Pasteur, 75 724 Paris, France
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Jean M. Kanellopoulos
Jean M. Kanellopoulos
Unité de Biologie Moléculaire du Gène, Institut National de la Sante et de la Recherche Medicale U277, Institut Pasteur, 75 724 Paris, France
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Jean-Pierre Cabaniols
Unité de Biologie Moléculaire du Gène, Institut National de la Sante et de la Recherche Medicale U277, Institut Pasteur, 75 724 Paris, France
Nicolas Fazilleau
Unité de Biologie Moléculaire du Gène, Institut National de la Sante et de la Recherche Medicale U277, Institut Pasteur, 75 724 Paris, France
Armanda Casrouge
Unité de Biologie Moléculaire du Gène, Institut National de la Sante et de la Recherche Medicale U277, Institut Pasteur, 75 724 Paris, France
Philippe Kourilsky
Unité de Biologie Moléculaire du Gène, Institut National de la Sante et de la Recherche Medicale U277, Institut Pasteur, 75 724 Paris, France
Jean M. Kanellopoulos
Unité de Biologie Moléculaire du Gène, Institut National de la Sante et de la Recherche Medicale U277, Institut Pasteur, 75 724 Paris, France
Address correspondence to J.M. Kanellopoulos, Unité de Biologie Moléculaire du Gène, INSERM U277, Institut Pasteur, 25 rue du docteur Roux, 75 724 Paris, France. Phone: 33-1-45-68-85-49; Fax: 33-1-45-68-85-48; E-mail: [email protected]
J.-P. Cabaniols and N. Fazilleau contributed equally to this work.
Received:
June 21 2001
Revision Received:
August 31 2001
Accepted:
September 20 2001
Online ISSN: 1540-9538
Print ISSN: 0022-1007
The Rockefeller University Press
2001
J Exp Med (2001) 194 (9): 1385–1390.
Article history
Received:
June 21 2001
Revision Received:
August 31 2001
Accepted:
September 20 2001
Citation
Jean-Pierre Cabaniols, Nicolas Fazilleau, Armanda Casrouge, Philippe Kourilsky, Jean M. Kanellopoulos; Most α/β T Cell Receptor Diversity Is Due to Terminal Deoxynucleotidyl Transferase . J Exp Med 5 November 2001; 194 (9): 1385–1390. doi: https://doi.org/10.1084/jem.194.9.1385
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