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Published online on February 27, 2004, 10.1073/pnas.0307827100
PNAS | March 9, 2004 | vol. 101 | no. 10 | 3480-3485


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Evolution
Codon usage between genomes is constrained by genome-wide mutational processes

Swaine L. Chen *, William Lee {dagger}, Alison K. Hottes, Lucy Shapiro, and Harley H. McAdams

Department of Developmental Biology, Stanford University School of Medicine, Beckman Center, B300, Stanford, CA 94304

Contributed by Lucy Shapiro, December 9, 2003

Analysis of genome-wide codon bias shows that only two parameters effectively differentiate the genome-wide codon bias of 100 eubacterial and archaeal organisms. The first parameter correlates with genome GC content, and the second parameter correlates with context-dependent nucleotide bias. Both of these parameters may be calculated from intergenic sequences. Therefore, genome-wide codon bias in eubacteria and archaea may be predicted from intergenic sequences that are not translated. When these two parameters are calculated for genes from nonmammalian eukaryotic organisms, genes from the same organism again have similar values, and genome-wide codon bias may also be predicted from intergenic sequences. In mammals, genes from the same organism are similar only in the second parameter, because GC content varies widely among isochores. Our results suggest that, in general, genome-wide codon bias is determined primarily by mutational processes that act throughout the genome, and only secondarily by selective forces acting on translated sequences.


Abbreviation: SVD, singular valve decomposition.

{dagger} Present address: Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305.

* To whom correspondence should be addressed. E-mail: slchen{at}stanford.edu.


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