Literature DB >> 1478894

Usage of human T-cell receptor V beta, J beta, C beta, and V alpha gene segments is not proportional to gene number.

M A Robinson1.   

Abstract

Certain T-cell receptor (TCR) beta-chain variable (V), joining (J), and constant (C) gene segments, as well as TCR alpha-chain V gene segments, are disproportionally represented in TCR alpha and beta cDNA libraries derived from PHA-stimulated peripheral blood lymphocytes. Sequences of 138 TCR alpha clones and 96 TCR beta clones were determined and of these 128 TCR alpha clones and 88 TCR beta clones were found to contain unique combinations of V, J, and C gene segments or to display diversity in N region nucleotides. The frequency of the V, J, and C genes used in the assembly of unique transcripts was ascertained. Of the 24 reported V beta gene families, 21 were observed among the 88 TCR beta clones including four V beta families (V beta 1, V beta 2, V beta 3, and V beta 4) that were represented in the sample 2 1/2-5 times more frequently than would be expected on the basis of copy number within the gene complex. Seventy-eight percent of the clones were positive for C beta 2 and more than half of the clones (53%) used one of two J beta 2 genes: J beta 2.1 was present in 27 clones and J beta 2.7 in 20 clones. TCR V alpha families were also disproportionately represented in this sample. Twenty-five of 30 V alpha families were observed in the sample of 128 clones including six recently reported V alpha families. Three V alpha families, V alpha 2, V alpha 8, and V alpha 23, accounted for approximately 40% of the TCR alpha clones and were represented at 18%, 9.4%, and 13.3%, respectively. Both V alpha 2 and V alpha 8 gene families contain more than one gene; thus the number of clones observed in these families may, in part, be related to gene number. However, V alpha 23, which appears to be a single-copy gene family, is significantly overrepresented in this sample. Although disproportional usage of V beta genes may be accounted for by superantigen exposure, reasons for disproportional usage of J beta, C beta, and V alpha genes are presently unknown.

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Year:  1992        PMID: 1478894     DOI: 10.1016/0198-8859(92)90095-5

Source DB:  PubMed          Journal:  Hum Immunol        ISSN: 0198-8859            Impact factor:   2.850


  7 in total

Review 1.  The genes influencing the susceptibility to IDDM in humans.

Authors:  S Faas; M Trucco
Journal:  J Endocrinol Invest       Date:  1994 Jul-Aug       Impact factor: 4.256

2.  Identification of the tumor cells in peripheral T-cell lymphomas by combined polymerase chain reaction-based T-cell receptor beta spectrotyping and immunohistological detection with T-cell receptor beta chain variable region segment-specific antibodies.

Authors:  Eva Geissinger; Irina Bonzheim; László Krenács; Sabine Roth; Philipp Ströbel; German Ott; Peter Reimer; Martin Wilhelm; Hans Konrad Müller-Hermelink; Thomas Rüdiger
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3.  Structure, diversity, and evolution of the T-cell receptor VB gene repertoire in primates.

Authors:  E E Jaeger; R E Bontrop; J S Lanchbury
Journal:  Immunogenetics       Date:  1994       Impact factor: 2.846

4.  Usage of TCRAV and TCRBV gene families in human fetal and adult TCR rearrangements.

Authors:  F M Raaphorst; J van Bergen; R L van den Bergh; M van der Keur; R de Krijger; J Bruining; M J van Tol; J M Vossen; P J van den Elsen
Journal:  Immunogenetics       Date:  1994       Impact factor: 2.846

5.  Genetic control of T cell receptor BJ gene expression in peripheral lymphocytes of normal and rheumatoid arthritis monozygotic twins.

Authors:  T Nanki; H Kohsaka; N Mizushima; W E Ollier; D A Carson; N Miyasaka
Journal:  J Clin Invest       Date:  1996-10-01       Impact factor: 14.808

6.  The human T cell antigen receptor repertoire: skewed use of V beta gene families by CD8+ T cells.

Authors:  G R Clarke; C A Humphrey; F C Lancaster; A W Boylston
Journal:  Clin Exp Immunol       Date:  1994-05       Impact factor: 4.330

7.  A genetically determined insertion/deletion related polymorphism in human T cell receptor beta chain (TCRB) includes functional variable gene segments.

Authors:  T M Zhao; S E Whitaker; M A Robinson
Journal:  J Exp Med       Date:  1994-10-01       Impact factor: 14.307

  7 in total

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