» Articles » PMID: 15598738

Mitochondrial Substitution Rates Are Extraordinarily Elevated and Variable in a Genus of Flowering Plants

Overview
Specialty Science
Date 2004 Dec 16
PMID 15598738
Citations 108
Authors
Affiliations
Soon will be listed here.
Abstract

Plant mitochondrial (mt) genomes have long been known to evolve slowly in sequence. Here we show remarkable departure from this pattern of conservative evolution in a genus of flowering plants. Substitution rates at synonymous sites vary substantially among lineages within Plantago. At the extreme, rates in Plantago exceed those in exceptionally slow plant lineages by approximately 4,000-fold. The fastest Plantago lineages set a new benchmark for rapid evolution in a DNA genome, exceeding even the fastest animal mt genome by an order of magnitude. All six mt genes examined show similarly elevated divergence in Plantago, implying that substitution rates are highly accelerated throughout the genome. In contrast, substitution rates show little or no elevation in Plantago for each of four chloroplast and three nuclear genes examined. These results, combined with relatively modest elevations in rates of nonsynonymous substitutions in Plantago mt genes, indicate that major, reversible changes in the mt mutation rate probably underlie the extensive variation in synonymous substitution rates. These rate changes could be caused by major changes in any number of factors that control the mt mutation rate, from the production and detoxification of oxygen free radicals in the mitochondrion to the efficacy of mt DNA replication and/or repair.

Citing Articles

Comparative genomics and phylogenetic analysis of mitochondrial genomes of Neocinnamomum.

Zhu W, Zhang D, Xu W, Gan Y, Huang J, Liu Y BMC Plant Biol. 2025; 25(1):289.

PMID: 40045193 PMC: 11883965. DOI: 10.1186/s12870-025-06238-x.


Mitochondrial genome of : features, RNA editing, and insights into male sterility.

Chen Z, Zhuo W, Wang Y, Qi J, Liu L, Lu S Front Plant Sci. 2025; 15:1520251.

PMID: 39866323 PMC: 11759266. DOI: 10.3389/fpls.2024.1520251.


Morphological and molecular characterization of two species of genus Ageratum.

Kumari A, Sidhu M Mol Biol Rep. 2024; 51(1):668.

PMID: 38787488 DOI: 10.1007/s11033-024-09582-7.


Genome copy number predicts extreme evolutionary rate variation in plant mitochondrial DNA.

Zwonitzer K, Tressel L, Wu Z, Kan S, Broz A, Mower J Proc Natl Acad Sci U S A. 2024; 121(10):e2317240121.

PMID: 38427600 PMC: 10927533. DOI: 10.1073/pnas.2317240121.


Remarkable mitochondrial genome heterogeneity in Meniocus linifolius (Brassicaceae).

Liu J, Hu J, Li D Plant Cell Rep. 2024; 43(2):36.

PMID: 38200362 DOI: 10.1007/s00299-023-03102-w.


References
1.
Laroche J, Bousquet J . Evolution of the mitochondrial rps3 intron in perennial and annual angiosperms and homology to nad5 intron 1. Mol Biol Evol. 1999; 16(4):441-52. DOI: 10.1093/oxfordjournals.molbev.a026126. View

2.
Bowe L, Coat G, dePamphilis C . Phylogeny of seed plants based on all three genomic compartments: extant gymnosperms are monophyletic and Gnetales' closest relatives are conifers. Proc Natl Acad Sci U S A. 2000; 97(8):4092-7. PMC: 18159. DOI: 10.1073/pnas.97.8.4092. View

3.
Bergthorsson U, Richardson A, Young G, Goertzen L, Palmer J . Massive horizontal transfer of mitochondrial genes from diverse land plant donors to the basal angiosperm Amborella. Proc Natl Acad Sci U S A. 2004; 101(51):17747-52. PMC: 539785. DOI: 10.1073/pnas.0408336102. View

4.
Brown W, Prager E, Wang A, Wilson A . Mitochondrial DNA sequences of primates: tempo and mode of evolution. J Mol Evol. 1982; 18(4):225-39. DOI: 10.1007/BF01734101. View

5.
Duff R, Nickrent D . Characterization of mitochondrial small-subunit ribosomal RNAs from holoparasitic plants. J Mol Evol. 1998; 45(6):631-9. DOI: 10.1007/pl00006267. View