Deterministic Mutation Rate Variation in the Human Genome
Open Access
- 1 September 2002
- journal article
- research article
- Published by Cold Spring Harbor Laboratory in Genome Research
- Vol. 12 (9) , 1350-1356
- https://doi.org/10.1101/gr.220502
Abstract
Several studies of substitution rate variation have indicated that the local mutation rate varies over the mammalian genome. In the present study, we show significant variation in substitution rates within the noncoding part of the human genome using 4.7 Mb of human-chimpanzee pairwise comparisons. Moreover, we find a significant positive covariation of lineage-specific chimpanzee and human local substitution rates, and very similar mean substitution rates down the two lineages. The substitution rate variation is probably not caused by selection or biased gene conversion, and so we conclude that mutation rates vary deterministically across the noncoding nonrepetitive regions of the human genome. We also show that noncoding substitution rates are significantly affected by G+C base composition, partly because the base composition is not at equilibrium.Keywords
This publication has 34 references indexed in Scilit:
- Construction and Analysis of a Human-Chimpanzee Comparative Clone MapScience, 2002
- Non–coding RNA genes and the modern RNA worldNature Reviews Genetics, 2001
- Comparison of genetic differentiation at marker loci and quantitative traitsJournal of Evolutionary Biology, 2001
- Evolutionarily Conserved Noncoding DNA in the Human Genome: How Much and What For?Genome Research, 2001
- A map of human genome sequence variation containing 1.42 million single nucleotide polymorphismsNature, 2001
- Initial sequencing and analysis of the human genomeNature, 2001
- Genomic Divergences between Humans and Other Hominoids and the Effective Population Size of the Common Ancestor of Humans and ChimpanzeesAmerican Journal of Human Genetics, 2001
- Gapped BLAST and PSI-BLAST: a new generation of protein database search programsNucleic Acids Research, 1997
- CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choiceNucleic Acids Research, 1994
- Mutation rates differ among regions of the mammalian genomeNature, 1989