Evidence map›Paper›PMID 30556907›Full record

ArticleThe New phytologist2019

Lycophyte plastid genomics: extreme variation in GC, gene and intron content and multiple inversions between a direct and inverted orientation of the rRNA repeat.

Jeffrey P Mower, Peng-Fei Ma, Felix Grewe, Alex Taylor, Todd P Michael, Robert VanBuren, Yin-Long Qiu

Open access · hybridAbstract read
In one paragraph

Article in The New phytologist, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
11.6field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

40 citing papers in PubMed, 69 citations in OpenAlex.

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  8. Extensive import of nucleus-encoded tRNAs into chloroplasts of the photosynthetic lycophyte,Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  9. Article
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  12. The complete chloroplast genome sequence ofMitochondrial DNA. Part B, Resources · 2024
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  13. Article
  14. Article
  15. The complete chloroplast genome of an Arctic lycophyte,Mitochondrial DNA. Part B, Resources · 2023
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 5 institutions in 2 countries.

Jeffrey P MowerCenter for Plant Science Innovation, University of Nebraska, Lincoln, NE, 68588, USA.ORCID 0000-0002-1501-5809
Peng-Fei MaCenter for Plant Science Innovation, University of Nebraska, Lincoln, NE, 68588, USA.
Felix GreweGrainger Bioinformatics Center, Science and Education, Field Museum of Natural History, Chicago, IL, 60605, USA.
Alex TaylorDepartment of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, MI, 48109, USA.
Todd P MichaelJ. Craig Venter Institute, La Jolla, CA, 92037, USA.ORCID 0000-0001-6272-2875
Robert VanBurenDepartment of Horticulture, Michigan State University, East Lansing, MI, 48824, USA.ORCID 0000-0003-2133-2760
Yin-Long QiuDepartment of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, MI, 48109, USA.
University of Michigan · USUniversity of Nebraska–Lincoln · USField Museum of Natural History · USJ. Craig Venter Institute · USMichigan State University · US

Funding

China Scholarship CouncilField MuseumUniversity of MichiganUniversity of Nebraska-Lincoln IC-2699
6 · The paper itself

Abstract

Lycophytes are a key group for understanding vascular plant evolution. Lycophyte plastomes are highly distinct, indicating a dynamic evolutionary history, but detailed evaluation is hindered by the limited availability of sequences. Eight diverse plastomes were sequenced to assess variation in structure and functional content across lycophytes. Lycopodiaceae plastomes have remained largely unchanged compared with the common ancestor of land plants, whereas plastome evolution in Isoetes and especially Selaginella is highly dynamic. Selaginella plastomes have the highest GC content and fewest genes and introns of any photosynthetic land plant. Uniquely, the canonical inverted repeat was converted into a direct repeat (DR) via large-scale inversion in some Selaginella species. Ancestral reconstruction identified additional putative transitions between an inverted and DR orientation in Selaginella and Isoetes plastomes. A DR orientation does not disrupt the activity of copy-dependent repair to suppress substitution rates within repeats. Lycophyte plastomes include the most archaic examples among vascular plants and the most reconfigured among land plants. These evolutionary trends correlate with the mitochondrial genome, suggesting shared underlying mechanisms. Copy-dependent repair for DR-localized genes indicates that recombination and gene conversion are not inhibited by the DR orientation. Gene relocation in lycophyte plastomes occurs via overlapping inversions rather than transposase/recombinase-mediated processes.

Indexed as

Genes, PlantGenetic VariationGenome, PlastidBase CompositionEvolution, MolecularGene DosageGenome SizeIntronsInverted Repeat SequencesLycopodiaceaePhylogenyRNA, RibosomalSelaginellaceaeRNA, Ribosomalevolutionary stasisgene lossinversionIsoetes (quillworts)Lycopodiaceae (clubmosses)Lycopodiophyta (lycophytes)plastid genome (plastome)Selaginella (spikemosses)

Identifiers

PMID30556907
PMCPMC6590440
OpenAlexW2905254662

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Registered trials

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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.