Literature DB >> 10427967

The central part of the mouse immunoglobulin kappa locus.

T Kirschbaum1, F Röschenthaler, A Bensch, B Hölscher, A Lautner-Rieske, M Ohnrich, S Pourrajabi, J Schwendinger, I Zocher, H G Zachau.   

Abstract

At the present state of analysis the central part of the kappa locus comprises four contigs of together 1.2 Mb and contains 55 Vkappa genes. It is flanked by the 3' part of the locus with 22 Vkappa genes in 0.4 Mb (T. Kirschbaum et al., Eur. J. Immunol. 1998. 28: 1458-1466) and the 5' part with 63 Vkappa genes in six contigs of together 1.5 Mb (F. Röschenthaler et al., accompanying report). The 5' and the central regions have one large contig in common. A part of the central region is linked to the 3' region resulting in a 1.1-Mb contig. The structure of the contigs was established mainly by the analysis of overlapping cosmid clones derived from genomic DNA and yeast and bacterial artificial chromosomes (YACs and BACs) and by PCR techniques. Pulsed-field gel electrophoresis of YAC digests indicated that three gaps between the contigs of the central region are 10-40 kb in size, comprising together about 90 kb. Internal duplications in this part of the locus and rearranged YACs were the major problems of the structural work. Structural details are to be found on the Internet at http://www.med.uni-muenchen.de/biochemie/zach au/kappa.htm. In a concluding section of the report the mouse kappa locus is compared to the human one and some aspects of the evolution of the kappa locus are discussed.

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Year:  1999        PMID: 10427967     DOI: 10.1002/(SICI)1521-4141(199907)29:07<2057::AID-IMMU2057>3.0.CO;2-P

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


  7 in total

1.  RNA surveillance down-regulates expression of nonfunctional kappa alleles and detects premature termination within the last kappa exon.

Authors:  Laurent Delpy; Christophe Sirac; Emmanuelle Magnoux; Sophie Duchez; Michel Cogné
Journal:  Proc Natl Acad Sci U S A       Date:  2004-05-03       Impact factor: 11.205

2.  Skewed primary Igκ repertoire and V-J joining in C57BL/6 mice: implications for recombination accessibility and receptor editing.

Authors:  Miyo Aoki-Ota; Ali Torkamani; Takayuki Ota; Nicholas Schork; David Nemazee
Journal:  J Immunol       Date:  2012-01-27       Impact factor: 5.422

3.  Differences in potential for amino acid change after mutation reveals distinct strategies for kappa and lambda light-chain variation.

Authors:  Uri Hershberg; Mark J Shlomchik
Journal:  Proc Natl Acad Sci U S A       Date:  2006-10-12       Impact factor: 11.205

4.  B cell receptors in TCL1 transgenic mice resemble those of aggressive, treatment-resistant human chronic lymphocytic leukemia.

Authors:  Xiao-jie Yan; Emilia Albesiano; Nicola Zanesi; Sophia Yancopoulos; Alan Sawyer; Egidio Romano; Aleksandar Petlickovski; Dimitar G Efremov; Carlo M Croce; Nicholas Chiorazzi
Journal:  Proc Natl Acad Sci U S A       Date:  2006-07-24       Impact factor: 11.205

5.  Exegesis: a procedure to improve gene predictions and its use to find immunoglobulin superfamily proteins in the human and mouse genomes.

Authors:  Bernard de Bono; Cyrus Chothia
Journal:  Nucleic Acids Res       Date:  2003-11-01       Impact factor: 16.971

6.  Assembly and analysis of the mouse immunoglobulin kappa gene sequence.

Authors:  Katherine M Brekke; William T Garrard
Journal:  Immunogenetics       Date:  2004-09-18       Impact factor: 2.846

Review 7.  Immunoglobulin Light Chain Gene Rearrangements, Receptor Editing and the Development of a Self-Tolerant Antibody Repertoire.

Authors:  Andrew M Collins; Corey T Watson
Journal:  Front Immunol       Date:  2018-10-08       Impact factor: 7.561

  7 in total

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