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Dog Special/Letter

Hotspots of mutation and breakage in dog and human chromosomes

MRC Functional Genetics Unit, Department of Human Anatomy and Genetics, University of Oxford, Oxford OX1 3QX, United Kingdom

ABSTRACT

Sequencing of the dog genome allows an investigation of the location-dependent evolutionary processes that occurred since the common ancestor of primates and carnivores, 95 million years ago. We investigated variations in G+C nucleotide fraction and synonymous nucleotide substitution rates (K_s) across dog and human genomes. Our results show that dog genes located either in subtelomeric and pericentromeric regions, or in short synteny blocks, possess significantly elevated G+C fraction and K_s values. Human subtelomeric, but not pericentromeric, genes also exhibit these elevations. We then examined 1.048 Gb of human sequence that is likely not to have been located near a primate telomere at any time since the common ancestor of dog and human. We observed that regions of highest G+C or K_s ("hotspots"; median sizes of 0.5 or 1.3 Mb, respectively) within this sequence were preferentially segregated to dog subtelomeres and pericentromeres during the rearrangements that eventually gave rise to the extant canine karyotype. Our data cannot be accounted for solely on the basis of gradually elevating G+C fractions in subtelomeric regions as a consequence of biased gene conversion. Rather, we propose that high G+C sequences are found preferentially within dog subtelomeres as a direct consequence of chromosomal fission occurring more frequently within regions elevated in G+C.

Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.3896805.

¹ Corresponding author.
E-mail caleb.webber{at}human-anatomy.oxford.ac.uk; fax 44-1865-282651.

[Supplemental material is available online at www.genome.org.]

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