Volume 184, Issue 1 p. 286-298

DNA methylation and Z-DNA formation as mediators of quantitative differences in the expression of alleles

Stefan Rothenburg

Stefan Rothenburg

Institute for Immunology, University Hospital Hamburg-Eppendorf, Hamburg, Germany

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Friedrich Koch-Nolte

Friedrich Koch-Nolte

Institute for Immunology, University Hospital Hamburg-Eppendorf, Hamburg, Germany

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Friedrich Haag

Corresponding Author

Friedrich Haag

Institute for Immunology, University Hospital Hamburg-Eppendorf, Hamburg, Germany

Correspondence to: Friedrich Haag
Institute for Immunology
University Hospital Hamburg-Eppendorf
Martinistr. 52
D-20246 Hamburg
Germany
Fax: 49 40 42803 4243
e-mail: [email protected]Search for more papers by this author
First published: 26 March 2002
Citations: 36

Abstract

Summary: With draft copies of several model genomes available in the near future, attention is turning towards the genetic mechanisms that determine differences between individuals. While mutations in protein coding regions affect the structure of gene products, polymorphisms outside such regions may cause quantitative differences in gene expression. Here we summarize observations indicating that such differences may be mediated by allele-specific alterations in the modification or structure of DNA. Mono-allelic expression of the rat T-cell differentiation marker RT6 in a subpopulation of cells is associated with allele-specific differences in DNA methylation in the RT6 promoter. In contrast to previously described examples of mono-allelic expression, these are determined neither stochastically nor by parental origin, but by cis-acting elements within the alleles. An attractive candidate is a rodent identifier (ID) element exclusively present in the RT6a allele. In the case of the rat nucleolin gene, a polymorphic dinucleotide repeat in the 5′ region modulates promoter strength and forms left-handed Z-DNA in vivo. Models explaining putative effects of Z-DNA formation on transcription are presented. These observations suggest novel mechanisms by which repetitive DNA, an abundant source of polymorphism in the mammalian genome, may exert quantitative effects on gene expression.

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