Literature DB >> 22056943

Evolution of coordinated mutagenesis and somatic hypermutation in VH5.

Barbara E Wright1, Karen H Schmidt, Aaron T Hunt, Dennis K Reschke, Michael F Minnick.   

Abstract

The VH5 human antibody gene was analyzed using a computer program (mfg) which simulates transcription, to better understand transcription-driven mutagenesis events that occur during "phase 1" of somatic hypermutation. Results show that the great majority of mutations in the non-transcribed strand occur within loops of two predicted high-stability stem-loop structures, termed SLSs 14.9 and 13.9. In fact, 89% of the 2505 mutations reported are within the encoded complementarity-determining region (CDR) and occur in loops of these high-stability structures. In vitro studies were also done and verified the existence of SLS 14.9. Following the formation of SLSs 14.9 and 13.9, a sustained period of transcriptional activity occurs within a window size of 60-70 nucleotides. During this period, the stability of these two SLSs does not change, and may provide the substrate for base exchanges and mutagenesis. The data suggest that many mutable bases are exposed simultaneously at pause sites, allowing for coordinated mutagenesis.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 22056943      PMCID: PMC3235918          DOI: 10.1016/j.molimm.2011.10.001

Source DB:  PubMed          Journal:  Mol Immunol        ISSN: 0161-5890            Impact factor:   4.407


  48 in total

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Authors:  B E Wright
Journal:  J Bacteriol       Date:  2000-06       Impact factor: 3.490

2.  Predicting mutation frequencies in stem-loop structures of derepressed genes: implications for evolution.

Authors:  Barbara E Wright; Dennis K Reschke; Karen H Schmidt; Jacqueline M Reimers; William Knight
Journal:  Mol Microbiol       Date:  2003-04       Impact factor: 3.501

Review 3.  Stress-directed adaptive mutations and evolution.

Authors:  Barbara E Wright
Journal:  Mol Microbiol       Date:  2004-05       Impact factor: 3.501

4.  Cutting edge: DGYW/WRCH is a better predictor of mutability at G:C bases in Ig hypermutation than the widely accepted RGYW/WRCY motif and probably reflects a two-step activation-induced cytidine deaminase-triggered process.

Authors:  Igor B Rogozin; Marilyn Diaz
Journal:  J Immunol       Date:  2004-03-15       Impact factor: 5.422

5.  Heat-induced deamination of cytosine residues in deoxyribonucleic acid.

Authors:  T Lindahl; B Nyberg
Journal:  Biochemistry       Date:  1974-07-30       Impact factor: 3.162

6.  Sequencing end-labeled DNA with base-specific chemical cleavages.

Authors:  A M Maxam; W Gilbert
Journal:  Methods Enzymol       Date:  1980       Impact factor: 1.600

7.  Hypermutable bases in the p53 cancer gene are at vulnerable positions in DNA secondary structures.

Authors:  Barbara E Wright; Jacqueline M Reimers; Karen H Schmidt; Dennis K Reschke
Journal:  Cancer Res       Date:  2002-10-15       Impact factor: 12.701

Review 8.  A/T-targeted somatic hypermutation: critique of the mainstream model.

Authors:  Andrew Franklin; Robert V Blanden
Journal:  Trends Biochem Sci       Date:  2006-04-17       Impact factor: 13.807

9.  Increased transcription rates correlate with increased reversion rates in leuB and argH Escherichia coli auxotrophs.

Authors:  Jacqueline M Reimers; Karen H Schmidt; Angelika Longacre; Dennis K Reschke; Barbara E Wright
Journal:  Microbiology       Date:  2004-05       Impact factor: 2.777

10.  The function of AID in somatic mutation and class switch recombination: upstream or downstream of DNA breaks.

Authors:  Katrin F Chua; Frederick W Alt; John P Manis
Journal:  J Exp Med       Date:  2002-05-06       Impact factor: 14.307

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  3 in total

1.  Stabilised DNA secondary structures with increasing transcription localise hypermutable bases for somatic hypermutation in IGHV3-23.

Authors:  Bhargavi Duvvuri; Venkata R Duvvuri; Jianhong Wu; Gillian E Wu
Journal:  Immunogenetics       Date:  2012-03-06       Impact factor: 2.846

2.  Gene Conversion-Like Events in the Diversification of Human Rearranged IGHV3-23*01 Gene Sequences.

Authors:  Bhargavi Duvvuri; Gillian E Wu
Journal:  Front Immunol       Date:  2012-06-15       Impact factor: 7.561

3.  Integrity of immunoglobulin variable regions is supported by GANP during AID-induced somatic hypermutation in germinal center B cells.

Authors:  Mohammed Mansour Abbas Eid; Mayuko Shimoda; Shailendra Kumar Singh; Sarah Ameen Almofty; Phuong Pham; Myron F Goodman; Kazuhiko Maeda; Nobuo Sakaguchi
Journal:  Int Immunol       Date:  2017-05-01       Impact factor: 4.823

  3 in total

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