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The Estimated Pacemaker for Great Apes Supports the Hominoid Slowdown Hypothesis
Beatriz Mello1, Carlos G Schrago1
1Department of Genetics, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Evolutionary Bioinformatics Online
|June 22, 2019
Summary
Great ape genomes show a predominant evolutionary trend, with most genes following a strict molecular clock. However, a slowdown in evolutionary rates was observed in human lineages, suggesting life history traits drive substitution rate variation.
Area of Science:
- Evolutionary biology
- Genomics
- Molecular evolution
Background:
- Genomic data reveals substitution rate variation across genomes and lineages.
- The pacemaker model suggests proportionality constants in evolutionary tree branch lengths due to lineage effects.
- Previous studies on the pacemaker hypothesis yielded contrasting results across different clades.
Purpose of the Study:
- To evaluate the pacemaker hypothesis for the first time in all great apes (hominids).
- To investigate whether evolutionary rates in hominids conform to a pacemaker model, considering gene tree/species tree discordance.
Main Methods:
- Substitution rates were estimated using a calibration-free approach, the relative rate framework.
- Pacemakers were inferred while accounting for gene tree/species tree discordance.
- Evolutionary rates were analyzed across genomic regions in great apes.
Main Results:
- A large pacemaker was identified in great apes, encompassing most hominid genomic regions, indicating a predominant evolutionary trend.
- The majority of genes exhibited evolutionary paces closely aligned with a strict molecular clock.
- Slight decreases in evolutionary rates were detected in internal branches leading to humans, supporting the hominoid slowdown hypothesis.
Conclusions:
- The study provides evidence for a predominant evolutionary pacemaker across most genomic regions in great apes.
- While most genes adhere to a molecular clock, a notable slowdown occurred in human lineages.
- Life history traits are suggested as the primary drivers of substitution rate variation across the great ape genome.
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