Phylogenomic inference in extremisA case study with mycoheterotroph plastomes

Awduron Sefydliadau
  • Vivienne K. Y. Lam(Awdur)
    University of British Columbia
  • Hayley Darby(Awdur)
    University of British Columbia
  • Vincent S. F. T. Merckx(Awdur)
    Naturalis Biodiversity Center
  • Gwynne Lim(Awdur)
    New York Botanical Garden
  • Tomohisa Yukawa(Awdur)
    Tsukuba Botanical Garden
  • Kurt M. Neubig(Awdur)
    Southern Illinois University
  • J. Richard Abbott(Awdur)
    University of St Andrews
  • Gemma Beatty(Awdur)
  • Jim Provan(Awdur)
  • Marybel Soto Gomez(Awdur)
    University of British Columbia
  • Sean W. Graham(Awdur)
    University of British Columbia
Math Erthygl
Iaith wreiddiolSaesneg
Tudalennau (o-i)480-494
Nifer y tudalennau15
CyfnodolynAmerican Journal of Botany
Cyfrol105
Rhif y cyfnodolyn3
Dyddiad ar-lein cynnar05 Mai 2018
Dangosyddion eitem ddigidol (DOIs)
StatwsCyhoeddwyd - 10 Mai 2018
Cysylltiadau
Cysylltiad parhaol
Arddangos ystadegau lawrlwytho
Gweld graff cysylltiadau
Fformatau enwi

Crynodeb

Premise of the Study
Phylogenomic studies employing large numbers of genes, including those based on plastid genomes (plastomes), are becoming common. Nonphotosynthetic plants such as mycoheterotrophs (which rely on root‐associated fungi for essential nutrients, including carbon) tend to have highly elevated rates of plastome evolution, substantial genome reduction, or both. Mycoheterotroph plastomes therefore provide excellent test cases for investigating how extreme conditions impact phylogenomic inference.

Methods
We used parsimony and likelihood analysis of protein‐coding gene sets from published and newly completed plastomes to infer the phylogenetic placement of taxa from the 10 angiosperm families in which mycoheterotrophy evolved.

Key Results
Despite multiple very long branches that reflect elevated substitution rates, and frequently patchy gene recovery due to genome reduction, inferred phylogenetic placements of most mycoheterotrophic lineages in DNA‐based likelihood analyses are both well supported and congruent with other studies. Amino‐acid‐based likelihood placements are broadly consistent with DNA‐based inferences, but extremely rate‐elevated taxa can have unexpected placements—albeit with weak support. In contrast, parsimony analysis is strongly misled by long‐branch attraction among many distantly related mycoheterotrophic monocots.

Conclusions
Mycoheterotrophic plastomes provide challenging cases for phylogenomic inference, as substitutional rates can be elevated and genome reduction can lead to sparse gene recovery. Nonetheless, diverse likelihood frameworks provide generally well‐supported and mutually concordant phylogenetic placements of mycoheterotrophs, consistent with recent phylogenetic studies and angiosperm‐wide classifications. Previous predictions of parallel photosynthesis loss within families are supported for Burmanniaceae, Ericaceae, Gentianaceae, and Orchidaceae. Burmanniaceae and Thismiaceae should not be combined as a single family in Dioscoreales.

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