1. Department of Biology, Indiana University, Bloomington, Indiana 47405, USA
2. Hubbard Center for Genome Studies, University of New Hampshire, Durham, New Hampshire 03824, USA

Correspondence to: Dee R. Denver¹ Email: ddenver@bio.indiana.edu

Abstract

Mutations have pivotal functions in the onset of genetic diseases and are the fundamental substrate for evolution. However, present estimates of the spontaneous mutation rate and spectrum are derived from indirect and biased measurements. For instance, mutation rate estimates for Caenorhabditis elegans are extrapolated from observations on a few genetic loci with visible phenotypes and vary over an order of magnitude¹. Alternative approaches in mammals, relying on phylogenetic comparisons of pseudogene loci² and fourfold degenerate codon positions³, suffer from uncertainties in the actual number of generations separating the compared species and the inability to exclude biases associated with natural selection. Here we provide a direct and unbiased estimate of the nuclear mutation rate and its molecular spectrum with a set of C. elegans mutation-accumulation lines that reveal a mutation rate about tenfold higher than previous indirect estimates and an excess of insertions over deletions. Because deletions dominate patterns of C. elegans pseudogene variation^{4, 5}, our observations indicate that natural selection might be significant in promoting small genome size, and challenge the prevalent assumption that pseudogene divergence accurately reflects the spontaneous mutation spectrum.

1. Department of Biology, Indiana University, Bloomington, Indiana 47405, USA
2. Hubbard Center for Genome Studies, University of New Hampshire, Durham, New Hampshire 03824, USA

Correspondence to: Dee R. Denver¹ Email: ddenver@bio.indiana.edu

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