Evidence map›Paper›PMID 22247429›Full record

ArticleGenome biology and evolution2012

Recent acceleration of plastid sequence and structural evolution coincides with extreme mitochondrial divergence in the angiosperm genus Silene.

Daniel B Sloan, Andrew J Alverson, Martin Wu, Jeffrey D Palmer, Douglas R Taylor

Abstract read
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Article in Genome biology and evolution, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

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85citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

85 citing papers in PubMed.

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  17. Comparative Genomics ofBiomolecules · 2025
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  18. The organelle genomes of the endangered seagrassFrontiers in plant science · 2025
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  19. Analysis of the mitochondrial genome of theFrontiers in plant science · 2025
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  20. Unveiling the complete organelle genomes ofFrontiers in plant science · 2025
    Article

25 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Daniel B SloanDepartment of Biology, University of Virginia, VA, USA. daniel.sloan@yale.edu
Andrew J Alverson
Martin Wu
Jeffrey D Palmer
Douglas R Taylor

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The angiosperm genus Silene exhibits some of the most extreme and rapid divergence ever identified in mitochondrial genome architecture and nucleotide substitution rates. These patterns have been considered mitochondrial specific based on the absence of correlated changes in the small number of available nuclear and plastid gene sequences. To better assess the relationship between mitochondrial and plastid evolution, we sequenced the plastid genomes from four Silene species with fully sequenced mitochondrial genomes. We found that two species with fast-evolving mitochondrial genomes, S. noctiflora and S. conica, also exhibit accelerated rates of sequence and structural evolution in their plastid genomes. The nature of these changes, however, is markedly different from those in the mitochondrial genome. For example, in contrast to the mitochondrial pattern, which appears to be genome wide and mutationally driven, the plastid substitution rate accelerations are restricted to a subset of genes and preferentially affect nonsynonymous sites, indicating that altered selection pressures are acting on specific plastid-encoded functions in these species. Indeed, some plastid genes in S. noctiflora and S. conica show strong evidence of positive selection. In contrast, two species with more slowly evolving mitochondrial genomes, S. latifolia and S. vulgaris, have correspondingly low rates of nucleotide substitution in plastid genes as well as a plastid genome structure that has remained essentially unchanged since the origin of angiosperms. These results raise the possibility that common evolutionary forces could be shaping the extreme but distinct patterns of divergence in both organelle genomes within this genus.

Indexed as

Evolution, MolecularDNA, MitochondrialGenome, MitochondrialGenome, PlantMagnoliopsidaMolecular Sequence DataPhylogenyPlastidsSileneDNA, Mitochondrial

Identifiers

PMID22247429
PMCPMC3318436

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.