De Novo Mutation Rate Variation and Its Determinants in Chlamydomonas

• Published in: Molecular biology and evolution Vol. 38; no. 9; pp. 3709 - 3723
• Main Authors: López-Cortegano, Eugenio, Craig, Rory J, Chebib, Jobran, Samuels, Toby, Morgan, Andrew D, Kraemer, Susanne A, Böndel, Katharina B, Ness, Rob W, Colegrave, Nick, Keightley, Peter D
• Format: Journal Article
• Language: English
• Published: United States Oxford University Press 01-09-2021
• Subjects: Analysis; Base Composition; Chlamydomonas - genetics; Chlamydomonas reinhardtii - genetics; Discoveries; Genetic aspects; Genomes; Genomics; Mutation; Mutation Accumulation; Mutation Rate; Natural selection; Raw materials; comparative mutability; mutation spectrum; mutation rate; mutation accumulation; Chlamydomonas incerta; Chlamydomonas reinhardtii
• ISSN: 1537-1719; 0737-4038; 1537-1719
• DOI: 10.1093/molbev/msab140

Abstract
De novo mutations are central for evolution, since they provide the raw material for natural selection by regenerating genetic variation. However, studying de novo mutations is challenging and is generally restricted to model species, so we have a limited understanding of the evolution of the mutation rate and spectrum between closely related species. Here, we present a mutation accumulation (MA) experiment to study de novo mutation in the unicellular green alga Chlamydomonas incerta and perform comparative analyses with its closest known relative, Chlamydomonas reinhardtii. Using whole-genome sequencing data, we estimate that the median single nucleotide mutation (SNM) rate in C. incerta is μ = 7.6 × 10−10, and is highly variable between MA lines, ranging from μ = 0.35 × 10−10 to μ = 131.7 × 10−10. The SNM rate is strongly positively correlated with the mutation rate for insertions and deletions between lines (r > 0.97). We infer that the genomic factors associated with variation in the mutation rate are similar to those in C. reinhardtii, allowing for cross-prediction between species. Among these genomic factors, sequence context and complexity are more important than GC content. With the exception of a remarkably high C→T bias, the SNM spectrum differs markedly between the two Chlamydomonas species. Our results suggest that similar genomic and biological characteristics may result in a similar mutation rate in the two species, whereas the SNM spectrum has more freedom to diverge.