Literature DB >> 1902859

Position of the rearranged V kappa and its 5' flanking sequences determines the location of somatic mutations in the J kappa locus.

J S Weber1, J Berry, T Manser, J L Claflin.   

Abstract

Somatic hypermutation is known to occur in the VJ kappa exon and its flanking sequences, yet little is known about the hypermutation mechanism or its exact target within the rearranged locus. Mutations may occur at the same frequency, spanning a region from the leader intron to 3' of J kappa 5, regardless of which J is chosen for VJ rearrangement. Another possibility is that mutations may be limited to the rearranged VJ kappa and its immediate flanking sequences. To distinguish between these possibilities, the JC introns of 21 alleles with V kappa rearranged to J kappa 1 were sequenced, and mutations were located. The frequency of mutations was determined for different sections of the intron and compared with the frequencies of mutations found in the JC intron of a set of VJ kappa 5 alleles. The results showed that mutations were concentrated in and around the rearranged VJ, regardless of whether J kappa 1 or J kappa 5 was used. These data imply that the hypermutational mechanism focuses on rearranged V genes.

Mesh:

Substances:

Year:  1991        PMID: 1902859

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  17 in total

1.  Indirect and direct evidence for DNA double-strand breaks in hypermutating immunoglobulin genes.

Authors:  H Jacobs; K Rajewsky; Y Fukita; L Bross
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2001-01-29       Impact factor: 6.237

Review 2.  The reverse transcriptase model of somatic hypermutation.

Authors:  E J Steele; R V Blanden
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2001-01-29       Impact factor: 6.237

3.  The intrinsic hypermutability of antibody heavy and light chain genes decays exponentially.

Authors:  C Rada; C Milstein
Journal:  EMBO J       Date:  2001-08-15       Impact factor: 11.598

Review 4.  Somatic diversification of antibody responses.

Authors:  B Zheng; G Kelsoe; S Han
Journal:  J Clin Immunol       Date:  1996-01       Impact factor: 8.317

5.  Modifying the sequence of an immunoglobulin V-gene alters the resulting pattern of hypermutation.

Authors:  B Goyenechea; C Milstein
Journal:  Proc Natl Acad Sci U S A       Date:  1996-11-26       Impact factor: 11.205

Review 6.  Activation-induced cytidine deaminase in antibody diversification and chromosome translocation.

Authors:  Anna Gazumyan; Anne Bothmer; Isaac A Klein; Michel C Nussenzweig; Kevin M McBride
Journal:  Adv Cancer Res       Date:  2012       Impact factor: 6.242

7.  An immunoglobulin mutator that targets G.C base pairs.

Authors:  J Bachl; M Wabl
Journal:  Proc Natl Acad Sci U S A       Date:  1996-01-23       Impact factor: 11.205

8.  Co-existence of somatic hypermutation and gene conversion in hypervariable regions of single Igkappa clones.

Authors:  J Liu; B Wolf
Journal:  Immunology       Date:  1998-10       Impact factor: 7.397

Review 9.  AID and Apobec3G haphazard deamination and mutational diversity.

Authors:  Malgorzata Jaszczur; Jeffrey G Bertram; Phuong Pham; Matthew D Scharff; Myron F Goodman
Journal:  Cell Mol Life Sci       Date:  2012-11-22       Impact factor: 9.261

10.  Mutation pattern of immunoglobulin transgenes is compatible with a model of somatic hypermutation in which targeting of the mutator is linked to the direction of DNA replication.

Authors:  B Rogerson; J Hackett; A Peters; D Haasch; U Storb
Journal:  EMBO J       Date:  1991-12       Impact factor: 11.598

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