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PMID: 9016873 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The transcriptional promoter regulates hypermutation of the antibody heavy chain locus.

The Journal of experimental medicine ·Vol. 185 ·No. 2 ·1997-01-20 ·Pages 239-50

Tumas-Brundage K, Manser T

Abstract

A somatic process introduces mutations into antibody variable (V) region genes at a high rate in many vertebrates, and is a major source of antibody diversity. The mechanism of this hypermutation process remains enigmatic, although retrospective studies and transgenic experiments have recently suggested a role for transcriptional regulatory elements. Here, we demonstrate that mouse heavy (H) chain loci in which the natural VH promoter has been replaced by a heterologous promoter undergo hypermutation. However, while the distribution of mutation in such loci appears normal, the frequency of mutation does not. Conversely, moving the VH promoter 750 bp upstream of its normal location results in a commensurate change in the site specificity of hypermutation in H chain loci, and the foreign DNA inserted into the VH leader intron to produce this promoter displacement is hypermutated in a manner indistinguishable from natural Ig DNA. These data establish a direct mechanistic link between the IgH transcription and hypermutation processes.

MeSH Terms
Animals Base Sequence DNA Founder Effect Immunoglobulin Heavy Chains/genetics Mice Mice, Inbred C3H Mice, Inbred C57BL Mice, Transgenic Molecular Sequence Data Mutation Promoter Regions, Genetic Transcription, Genetic
Chemicals
Immunoglobulin Heavy Chains DNA
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Tumas-Brundage K
Department of Microbiology and Immunology, Kimmel Cancer Institute, Thomas Jefferson Medical College, Philadelphia, Pennsylvania 19107, USA.
Manser T
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35 references, click to expand
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Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1997-01-20
Pages
239-50
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2196128
Subset
IM
Grants
NIAID NIH HHS · AI23739 · United States
NCI NIH HHS · CA09683 · United States
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