Literature DB >> 6766210

The joining of V and J gene segments creates antibody diversity.

M Weigert, R Perry, D Kelley, T Hunkapiller, J Schilling, L Hood.   

Abstract

The variable regions of mouse kappa (kappa) chains are coded for by multiple variable (V) gene segments and multiple joining (J) gene segments. The V kappa gene segments code for residues 1 to 95; the J kappa gene segments code for residues 96 to 108 (refs 1-3). This gene organisation is similar to that encoding the V lambda regions. Diversity in V kappa regions arises from several sources: (1) there are multiple germ-line V kappa gene segments and J kappa gene segments; (2) combinatorial joining of V kappa gene segments with different germline J kappa gene segments; and possibly, (3) somatic point mutation, as postulated for V lambda gene segments. Also, from a comparison of the number of germ-line J kappa gene segments and amino acid sequences, it has been suggested that J kappa region sequences may be determined by the way V kappa and J kappa gene segments are joined. This report supports this model by directly associating various J kappa sequences with given J kappa gene segments.

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Year:  1980        PMID: 6766210     DOI: 10.1038/283497a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  44 in total

Review 1.  Relative roles of somatic and Darwinian evolution in shaping the antibody response.

Authors:  M Diaz; N R Klinman
Journal:  Immunol Res       Date:  2000       Impact factor: 2.829

2.  Somatic diversification of chicken immunoglobulin light chains by point mutations.

Authors:  R Parvari; E Ziv; F Lantner; D Heller; I Schechter
Journal:  Proc Natl Acad Sci U S A       Date:  1990-04       Impact factor: 11.205

Review 3.  Prognostic usage of V(H) gene mutation status and its surrogate markers and the role of antigen selection in chronic lymphocytic leukemia.

Authors:  Gerard Tobin; Richard Rosenquist
Journal:  Med Oncol       Date:  2005       Impact factor: 3.064

4.  Diversity and structure of human T-cell receptor beta-chain variable region genes.

Authors:  P Concannon; L A Pickering; P Kung; L Hood
Journal:  Proc Natl Acad Sci U S A       Date:  1986-09       Impact factor: 11.205

5.  Somatic evolution of variable region structures during an immune response.

Authors:  L Wysocki; T Manser; M L Gefter
Journal:  Proc Natl Acad Sci U S A       Date:  1986-03       Impact factor: 11.205

6.  Misalignment of V and J gene segments resulting in a nonfunctional immunoglobulin gene.

Authors:  A Walfield; E Selsing; B Arp; U Storb
Journal:  Nucleic Acids Res       Date:  1981-03-11       Impact factor: 16.971

7.  Analysis of immunoglobulin heavy chain V-region genes belonging to the V NP-gene family.

Authors:  T Blankenstein; G Zoebelein; U Krawinkel
Journal:  Nucleic Acids Res       Date:  1984-09-11       Impact factor: 16.971

Review 8.  Developmental aspects of B-cell repertoire phenotype.

Authors:  M P Cancro; M A Thompson; D M Hilbert
Journal:  Surv Immunol Res       Date:  1983

9.  Human self-protein CD8+ T-cell epitopes are both positively and negatively selected.

Authors:  Michal Almani; Shai Raffaeli; Tal Vider-Shalit; Lea Tsaban; Vered Fishbain; Yoram Louzoun
Journal:  Eur J Immunol       Date:  2009-04       Impact factor: 5.532

10.  Restricted association of V and J-C gene segments for mouse lambda chains.

Authors:  E B Reilly; B Blomberg; T Imanishi-Kari; S Tonegawa; H N Eisen
Journal:  Proc Natl Acad Sci U S A       Date:  1984-04       Impact factor: 11.205

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