- THIS ARTICLE
- Full Text (PDF)
- Alert me when this article is cited
- Alert me if a correction is posted
- SERVICES
- Similar articles in this journal
- Similar articles in PubMed
- Alert me to new issues of the journal
- Download to citation manager
- Reprints & Permissions
- CITING ARTICLES
- Citing Articles via HighWire
- Citing Articles via Google Scholar
- GOOGLE SCHOLAR
- Articles by Golding, G. B.
- Articles by Glickman, B. W.
- Search for Related Content
- PUBMED
- PubMed Citation
- Articles by Golding, G. B.
- Articles by Glickman, B. W.
Patterns of Somatic Mutations in Immunoglobulin Variable Genes
G. Brian Golding 1, Patricia J. Gearhart 2, and Barry W. Glickman 1
1 Department of Biology, York University, Toronto, Ontario,
Canada M3J 1P3
2 Department of Biochemistry, The Johns Hopkins University,
Baltimore, Maryland 21205
The mechanism responsible for somatic mutation in the variable genes of antibodies is unknown and may differ from previously described mechanisms that produce mutation in DNA. We have analyzed 421 somatic mutations from the rearranged immunoglobulin variable genes of mice to determine (1) if the nucleotide substitutions differ from those generated during meiosis and (2) if the presence of nearby direct and inverted repeated sequences could template mutations around the variable gene. The results reveal a difference in the pattern of substitutions obtained from somatic mutations vs. meiotic mutations. An increased frequency of T:A to C:G transitions and a decreased frequency of mutations involving a G in the somatic mutants compared to the meiotic mutants is indicated. This suggests that the mutational processes responsible for somatic mutation in antibody genes differs from that responsible for mutation during meiosis. An analysis of the local DNA sequences revealed many direct repeats and palindromic sequences that were capable of templating some of the known mutations. Although additional factors may be involved in targeting mutations to the variable gene, mistemplating by nearby repeats may provide a mechanism for the enhancement of somatic mutation.
Submitted on May 29, 1986Accepted on September 12, 1986
This article has been cited by other articles:
![]() |
J. Spencer and D. K. Dunn-Walters Hypermutation at A-T Base Pairs: The A Nucleotide Replacement Spectrum Is Affected by Adjacent Nucleotides and There Is No Reverse Complementarity of Sequences Flanking Mutated A and T Nucleotides J. Immunol., October 15, 2005; 175(8): 5170 - 5177. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Kotani, I.-m. Okazaki, M. Muramatsu, K. Kinoshita, N. A. Begum, T. Nakajima, H. Saito, and T. Honjo A target selection of somatic hypermutations is regulated similarly between T and B cells upon activation-induced cytidine deaminase expression PNAS, March 22, 2005; 102(12): 4506 - 4511. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Kodera, D. Radu, T. McGaha, P. Zwolo, C. Stoica, H. Cheroute, R. R Pollock, and C. Bona Cellular and molecular studies of B cells exhibiting reverse somatic mutation throughout life Genes Cells, November 1, 2004; 9(11): 1005 - 1016. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Martin and M. D. Scharff Somatic hypermutation of the AID transgene in B and non-B cells PNAS, September 17, 2002; 99(19): 12304 - 12308. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. S. Shapiro, K. Aviszus, J. Murphy, and L. J. Wysocki Evolution of Ig DNA Sequence to Target Specific Base Positions Within Codons for Somatic Hypermutation J. Immunol., March 1, 2002; 168(5): 2302 - 2306. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Diaz, L. K. Verkoczy, M. F. Flajnik, and N. R. Klinman Decreased Frequency of Somatic Hypermutation and Impaired Affinity Maturation but Intact Germinal Center Formation in Mice Expressing Antisense RNA to DNA Polymerase {{zeta}} J. Immunol., July 1, 2001; 167(1): 327 - 335. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Oprea, L. G. Cowell, and T. B. Kepler The Targeting of Somatic Hypermutation Closely Resembles That of Meiotic Mutation J. Immunol., January 15, 2001; 166(2): 892 - 899. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. S. Shapiro, K. Aviszus, D. Ikle, and L. J. Wysocki Predicting Regional Mutability in Antibody V Genes Based Solely on Di- and Trinucleotide Sequence Composition J. Immunol., July 1, 1999; 163(1): 259 - 268. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Diaz, J. Velez, M. Singh, J. Cerny, and M. F. Flajnik Mutational pattern of the nurse shark antigen receptor gene (NAR) is similar to that of mammalian Ig genes and to spontaneous mutations in evolution: the translesion synthesis model of somatic hypermutation Int. Immunol., May 1, 1999; 11(5): 825 - 833. [Abstract] [Full Text] [PDF] |
||||
![]() |
H.-Z. Peng, M.-Q. Du, A. Koulis, A. Aiello, A. Dogan, L.-X. Pan, and P. G. Isaacson Nonimmunoglobulin Gene Hypermutation in Germinal Center B Cells Blood, April 1, 1999; 93(7): 2167 - 2172. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Pasqualucci, A. Migliazza, N. Fracchiolla, C. William, A. Neri, L. Baldini, R. S. K. Chaganti, U. Klein, R. Kuppers, K. Rajewsky, et al. BCL-6 mutations in normal germinal center B cells: Evidence of somatic hypermutation acting outside Ig loci PNAS, September 29, 1998; 95(20): 11816 - 11821. [Abstract] [Full Text] [PDF] |
||||
![]() |
U. Storb, E. L. Klotz, J. Hackett Jr., K. Kage, G. Bozek, and T. E. Martin A Hypermutable Insert in an Immunoglobulin Transgene Contains Hotspots of Somatic Mutation and Sequences Predicting Highly Stable Structures in the RNA Transcript J. Exp. Med., August 17, 1998; 188(4): 689 - 698. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. B. Winter, Q. H. Phung, A. Umar, S. M. Baker, R. E. Tarone, K. Tanaka, R. M. Liskay, T. A. Kunkel, V. A. Bohr, and P. J. Gearhart Altered spectra of hypermutation in antibodies from mice deficient for the DNA mismatch repair protein PMS2 PNAS, June 9, 1998; 95(12): 6953 - 6958. [Abstract] [Full Text] [PDF] |
||||
![]() |
Q. H. Phung, D. B. Winter, A. Cranston, R. E. Tarone, V. A. Bohr, R. Fishel, and P. J. Gearhart Increased Hypermutation at G and C Nucleotides in Immunoglobulin Variable Genes from Mice Deficient in the MSH2 Mismatch Repair Protein J. Exp. Med., June 1, 1998; 187(11): 1745 - 1751. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. C. Wilson, O. d. Bouteiller, Y.-J. Liu, K. Potter, J. Banchereau, J. D. Capra, and V. Pascual Somatic Hypermutation Introduces Insertions and Deletions into Immunoglobulin V Genes J. Exp. Med., January 5, 1998; 187(1): 59 - 70. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. M.-Q. Lin, M. Zhu, and M. D. Scharff Sequence dependent hypermutation of the immunoglobulin heavy chain in cultured B cells PNAS, May 13, 1997; 94(10): 5284 - 5289. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Goyenechea and C. Milstein Modifying the sequence of an immunoglobulin V-gene alters the resulting pattern of hypermutation PNAS, November 26, 1996; 93(24): 13979 - 13984. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. E. Donelson and J. E. Donelson Mechanisms of Antigenic Variation in Borrelia hermsii and African Trypanosomes J. Biol. Chem., April 7, 1995; 270(14): 7783 - 7786. [Full Text] [PDF] |
||||
![]() |
D. French, R Laskov, and M. Scharff The role of somatic hypermutation in the generation of antibody diversity Science, June 9, 1989; 244(4909): 1152 - 1157. [Abstract] [PDF] |
||||







