Journal of Molecular Evolution

, Volume 71, Issue 5, pp 444–457

Selection and the Cell Cycle: Positive Darwinian Selection in a Well-Known DNA Damage Response Pathway


DOI: 10.1007/s00239-010-9399-y

Cite this article as:
O’Connell, M.J. J Mol Evol (2010) 71: 444. doi:10.1007/s00239-010-9399-y


Cancer is a common occurrence in multi-cellular organisms and is not strictly limited to the elderly in a population. It is therefore possible that individuals with genotypes that protect against early onset cancers have a selective advantage. In this study the patterns of mutation in the proteins of a well-studied DNA damage response pathway have been examined for evidence of adaptive evolutionary change. Using a maximum likelihood framework and the mammalian species phylogeny, together with codon models of evolution, selective pressure variation across the interacting network of proteins has been detected. The presence of signatures of adaptive evolution in BRCA1 and BRCA2 has already been documented but the effect on the entire network of interacting proteins in this damage response pathway has, until now, been unknown. Positive selection is evident throughout the network with a total of 11 proteins out of 15 examined displaying patterns of substitution characteristic of positive selection. It is also shown here that modern human populations display evidence of an ongoing selective sweep in 9 of these DNA damage repair proteins. The results presented here provide the community with new residues that may be relevant to cancer susceptibility while also highlighting those proteins where human and mouse have undergone lineage-specific functional shift. An understanding of this damage response pathway from an evolutionary perspective will undoubtedly contribute to future cancer treatment approaches.


Cell cycleCancer evolutionCancer selectionTumor suppressorBreast cancerPositive selectionAdaptive evolutionDNA repairVertebrate evolution

Supplementary material

239_2010_9399_MOESM1_ESM.doc (308 kb)
Supplementary material 1 (DOC 308 kb)
239_2010_9399_MOESM2_ESM.pdf (436 kb)
Supplementary material 2 (PDF 436 kb)
239_2010_9399_MOESM3_ESM.pdf (2.4 mb)
Supplementary material 3 (PDF 2421 kb)

Copyright information

© Springer Science+Business Media, LLC 2010

Authors and Affiliations

  1. 1.Bioinformatics and Molecular Evolution Group, School of BiotechnologyDublin City UniversityDublin 9Ireland
  2. 2.Centre for Scientific Computing & Complex Systems Modelling (SCI-SYM)Dublin City UniversityDublin 9Ireland