On the number of genomic pacemakers: a geometric approach.

The universal pacemaker (UPM) model extends the classical molecular clock (MC) model, by allowing each gene, in addition to its individual intrinsic rate as in the MC, to accelerate or decelerate according to the universal pacemaker. Under UPM, the relative evolutionary rates of all genes remain nearly constant whereas the absolute rates can change arbitrarily. It was shown on several taxa groups spanning the entire tree of life that the UPM model describes the evolutionary process better than the MC model. In this work we provide a natural generalization to the UPM model that we denote multiple pacemakers (MPM). Under the MPM model every gene is still affected by a single pacemaker, however the number of pacemakers is not confined to one. Such a model induces a partition over the gene set where all the genes in one part are affected by the same pacemaker and task is to identify the pacemaker partition, or in other words, finding for each gene its associated pacemaker. We devise a novel heuristic procedure, relying on statistical and geometrical tools, to solve the problem and demonstrate by simulation that this approach can cope satisfactorily with considerable noise and realistic problem sizes. We applied this procedure to a set of over 2000 genes in 100 prokaryotes and demonstrated the significant existence of two pacemakers.