Literature DB >> 20610427

Evolutionary rates of mitochondrial genomes correspond to diversification rates and to contemporary species richness in birds and reptiles.

Soo Hyung Eo1, J Andrew DeWoody.   

Abstract

Rates of biological diversification should ultimately correspond to rates of genome evolution. Recent studies have compared diversification rates with phylogenetic branch lengths, but incomplete phylogenies hamper such analyses for many taxa. Herein, we use pairwise comparisons of confamilial sauropsid (bird and reptile) mitochondrial DNA (mtDNA) genome sequences to estimate substitution rates. These molecular evolutionary rates are considered in light of the age and species richness of each taxonomic family, using a random-walk speciation-extinction process to estimate rates of diversification. We find the molecular clock ticks at disparate rates in different families and at different genes. For example, evolutionary rates are relatively fast in snakes and lizards, intermediate in crocodilians and slow in turtles and birds. There was also rate variation across genes, where non-synonymous substitution rates were fastest at ATP8 and slowest at CO3. Family-by-gene interactions were significant, indicating that local clocks vary substantially among sauropsids. Most importantly, we find evidence that mitochondrial genome evolutionary rates are positively correlated with speciation rates and with contemporary species richness. Nuclear sequences are poorly represented among reptiles, but the correlation between rates of molecular evolution and species diversification also extends to 18 avian nuclear genes we tested. Thus, the nuclear data buttress our mtDNA findings.

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Year:  2010        PMID: 20610427      PMCID: PMC2982251          DOI: 10.1098/rspb.2010.0965

Source DB:  PubMed          Journal:  Proc Biol Sci        ISSN: 0962-8452            Impact factor:   5.349


  29 in total

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3.  A mitogenomic timescale for birds detects variable phylogenetic rates of molecular evolution and refutes the standard molecular clock.

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Review 5.  Estimating diversification rates from phylogenetic information.

Authors:  Robert E Ricklefs
Journal:  Trends Ecol Evol       Date:  2007-10-25       Impact factor: 17.712

6.  Rates of nucleotide substitution in Cornaceae (Cornales)-Pattern of variation and underlying causal factors.

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Journal:  Mol Phylogenet Evol       Date:  2008-07-19       Impact factor: 4.286

7.  A phylogenomic study of birds reveals their evolutionary history.

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8.  Pseudogenes as a paradigm of neutral evolution.

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Authors:  John J Welch; Olaf R P Bininda-Emonds; Lindell Bromham
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  43 in total

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3.  Slow and steady: the evolution of cranial disparity in fossil and recent turtles.

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Journal:  Proc Biol Sci       Date:  2016-11-30       Impact factor: 5.349

Review 4.  Molecular evolution and the latitudinal biodiversity gradient.

Authors:  E J Dowle; M Morgan-Richards; S A Trewick
Journal:  Heredity (Edinb)       Date:  2013-03-13       Impact factor: 3.821

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6.  Integration of mtDNA pseudogenes into the nuclear genome coincides with speciation of the human genus. A hypothesis.

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Review 7.  The genetics of sex chromosomes: evolution and implications for hybrid incompatibility.

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8.  Phylogeography, Population Structure, and Species Delimitation in Rockhopper Penguins (Eudyptes chrysocome and Eudyptes moseleyi).

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Journal:  J Hered       Date:  2019-12-17       Impact factor: 2.645

9.  Speciation in little: the role of range and body size in the diversification of Malagasy mantellid frogs.

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10.  Sp7/Osterix Is Restricted to Bone-Forming Vertebrates where It Acts as a Dlx Co-factor in Osteoblast Specification.

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