4.7 Article

Most α/β T cell receptor diversity is due to terminal deoxynucleotidyl transferase

期刊

JOURNAL OF EXPERIMENTAL MEDICINE
卷 194, 期 9, 页码 1385-1390

出版社

ROCKEFELLER UNIV PRESS
DOI: 10.1084/jem.194.9.1385

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T cell repertoire; T cell receptor; knockout mice; terminal deoxynucleotidyl transferase; CDR3

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The contribution of template-independent nucleotide addition to antigen receptor diversity is unknown. We therefore determined the size of the T cell receptor (TCR)alpha/beta 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 degrees/degrees mice, TCRAV diversity is one order of magnitude lower than the TCRBV diversity. In Tdt degrees/degrees animals, TCRBV chain diversity is reduced 10-fold compared with wild-type mice. In addition, in Tdt degrees/degrees mice, one BV chain can associate with three to four AV chains as in wild-type mice. The alpha/beta repertoire size in Tdt degrees/degrees mice is estimated to be 10(5) distinct receptors, similar to5-10% of that calculated for wild-type mice. Thus, while Tdt activity is not involved in the combinatorial diversity resulting from alpha/beta pairing, it contributes to at least 90% of TCR alpha/beta diversity.

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