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MBE Advance Access originally published online on October 29, 2008
Molecular Biology and Evolution 2009 26(1):131-142; doi:10.1093/molbev/msn245
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© The Author 2008. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. All rights reserved. For permissions, please e-mail: journals.permissions@oxfordjournals.org

Research Articles

Transcription-Induced Mutational Strand Bias and Its Effect on Substitution Rates in Human Genes

Carina F. Mugal1, Hans-Hennig von Grünberg1 and Martin Peifer2

Institute of Chemistry, Karl-Franzens University Graz, Graz, Austria

E-mail: peifer{at}nf.mpg.de.

Accepted for publication October 7, 2008.

If substitution rates are not the same on the two complementary DNA strands, a substitution is considered strand asymmetric. Such substitutional strand asymmetries are determined here for the three most frequent types of substitution on the human genome (C -> T, A -> G, and G -> T). Substitution rate differences between both strands are estimated for 4,590 human genes by aligning all repeats occurring within the introns with their ancestral consensus sequences. For 1,630 of these genes, both coding strand and noncoding strand rates could be compared with rates in gene-flanking regions. All three rates considered are found to be on average higher on the coding strand and lower on the transcribed strand in comparison to their values in the gene-flanking regions. This finding points to the simultaneous action of rate-increasing effects on the coding strand—such as increased adenine and cytosine deamination—and transcription-coupled repair as a rate-reducing effect on the transcribed strand. The common behavior of the three rates leads to strong correlations of the rate asymmetries: Whenever one rate is strand biased, the other two rates are likely to show the same bias. Furthermore, we determine all three rate asymmetries as a function of time: the A -> G and G -> T rate asymmetries are both found to be constant in time, whereas the C -> T rate asymmetry shows a pronounced time dependence, an observation that explains the difference between our results and those of an earlier work by Green et al. (2003. Transcription-associated mutational asymmetry in mammalian evolution. Nat Genet. 33:514–517.). Finally, we show that in addition to transcription also the replication process biases the substitution rates in genes.

Key Words: substitution rate asymmetries • transcription-coupled repair • cytosine deamination


1 Present address: Institute of Chemistry, Karl-Franzens University Graz, Graz, Austria.

2 Present address: Max-Planck Institute for Neurological Research, Cologne, Germany.

Manolo Gouy, Associate Editor


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