Literature DB >> 7925568

Comparison of the J beta gene usage among different T cell receptor V beta families in spleens of C57BL/6 mice.

T Kato1, S Suzuki, H Sasakawa, K Masuko, Y Ikeda, K Nishioka, K Yamamoto.   

Abstract

To clarify whether there is a bias in the V-D-J combination of T cell receptor (TcR) genes, J beta gene usage has been investigated in a total of 743 TcR beta genes of V beta 2, V beta 8.2, and V beta 14 families expressed in C57BL/6 mouse spleens. Genes of TcR beta chains, amplified by a reverse transcriptase-polymerase chain reaction, were individually cloned into plasmids. Cloned genes (61 to 106), randomly selected in each respective V beta family from three different mice, were tested by means of hybridization with 12 oligo DNA probes which were designed to differentiate 12 murine functional J beta gene segments. The results are enumerated below. (1) The J beta 2.6 gene segment was found to be most frequently used (V beta 2, 19.8%; V beta 8.2, 21.2%; and V beta 14, 19.2%). In contrast, usage of the J beta 1.6 gene segment was most infrequent (V beta 2, 1.9%; V beta 8.2, 2.9%; and V beta 14, 0.5%); (2) High frequency of the J beta 2.1 gene segment and low frequency of the J beta 1.3 and J beta 1.5 gene segments were also observed; (3) The J beta 2 cluster was used in preference to the J beta 1 cluster (usages of the J beta 2 cluster: V beta 2, 67.8%; V beta 8.2, 65.9%; and V beta 14, 70.4%); and (4) These biases were generally common to all three V beta families examined and differences among individual mice were mostly small. Considering these findings, we conclude that the TcR J beta gene segments in C57BL/6 mice splenocytes are selected with a bias, but are selected independently of the V beta families.

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Year:  1994        PMID: 7925568     DOI: 10.1002/eji.1830241022

Source DB:  PubMed          Journal:  Eur J Immunol        ISSN: 0014-2980            Impact factor:   5.532


  7 in total

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Authors:  Elizabeth D Hughes; Yun Yan Qu; Suzanne J Genik; Robert H Lyons; Christopher D Pacheco; Andrew P Lieberman; Linda C Samuelson; Igor O Nasonkin; Sally A Camper; Margaret L Van Keuren; Thomas L Saunders
Journal:  Mamm Genome       Date:  2007-09-09       Impact factor: 2.957

2.  Natural killer T cells reactive to a single glycolipid exhibit a highly diverse T cell receptor beta repertoire and small clone size.

Authors:  J L Matsuda; L Gapin; N Fazilleau; K Warren; O V Naidenko; M Kronenberg
Journal:  Proc Natl Acad Sci U S A       Date:  2001-10-09       Impact factor: 11.205

3.  Evolutionarily conserved pattern of gene segment usage within the mammalian TCRbeta locus.

Authors:  Ferenc Livák
Journal:  Immunogenetics       Date:  2003-07-04       Impact factor: 2.846

4.  Chromatin conformation governs T-cell receptor Jβ gene segment usage.

Authors:  Wilfred Ndifon; Hilah Gal; Eric Shifrut; Rina Aharoni; Nissan Yissachar; Nir Waysbort; Shlomit Reich-Zeliger; Ruth Arnon; Nir Friedman
Journal:  Proc Natl Acad Sci U S A       Date:  2012-09-10       Impact factor: 11.205

5.  Convergent recombination shapes the clonotypic landscape of the naive T-cell repertoire.

Authors:  Máire F Quigley; Hui Yee Greenaway; Vanessa Venturi; Ross Lindsay; Kylie M Quinn; Robert A Seder; Daniel C Douek; Miles P Davenport; David A Price
Journal:  Proc Natl Acad Sci U S A       Date:  2010-10-25       Impact factor: 11.205

6.  Most alpha/beta T cell receptor diversity is due to terminal deoxynucleotidyl transferase.

Authors:  J P Cabaniols; N Fazilleau; A Casrouge; P Kourilsky; J M Kanellopoulos
Journal:  J Exp Med       Date:  2001-11-05       Impact factor: 14.307

7.  The application of real-time PCR to the analysis of T cell repertoires.

Authors:  Peter Wettstein; Michael Strausbauch; Terry Therneau; Nancy Borson
Journal:  Nucleic Acids Res       Date:  2008-10-03       Impact factor: 16.971

  7 in total

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