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Updated: Apr 16, 2026

Genome-wide Determination of Mammalian Replication Timing by DNA Content Measurement
Published on: January 19, 2017
Mammalian genome evolution is governed by multiple pacemakers
Sebastián Duchêne1, Simon Y W Ho1
1School of Biological Sciences, University of Sydney, Sydney, NSW 2006, Australia.
Genomic evolution shows rate variation across genes and lineages, explained by 13 "pacemakers" supporting the Multiple Pacemaker model. This finding impacts understanding genome evolution and molecular clock analyses.
Area of Science:
- Evolutionary biology
- Genomics
- Phylogenetics
Background:
- Genomic evolution is driven by mutation, selection, and genetic drift, causing rate variation across genes and lineages.
- Interactions between these variations can lead to residual effects, where rate heterogeneity patterns differ across genes.
- Pacemaker models describe genome evolution rate variation, differing in the significance of residual effects: Universal, Multiple, and Degenerate Multiple Pacemaker models.
Purpose of the Study:
- To compare different pacemaker models of genome evolution.
- To partition and analyze rate variation across loci using a phylogenetic method.
- To investigate the factors driving genomic evolution and inform molecular-clock analyses.
Main Methods:
- Phylogenetic analysis to partition evolutionary rate variation across loci.
- Comparison of Universal, Multiple, and Degenerate Multiple Pacemaker models.
- Analysis of 431 genes from 29 mammalian taxa.
Main Results:
- The study identified 13 distinct pacemakers, supporting the Multiple Pacemaker model of genome evolution.
- Rate variation across the analyzed mammalian genes is explained by these 13 pacemakers.
- No correlation was found between identified pacemakers and specific gene functions.
Conclusions:
- The Multiple Pacemaker model best explains the observed rate variation in mammalian genome evolution.
- The findings provide insights into the complex factors shaping genomic evolution.
- Results have implications for the accuracy and interpretation of molecular-clock dating.
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