Evidence map›Paper›PMID 22194700›Full record

ArticlePLoS genetics2011

A functional phylogenomic view of the seed plants.

Ernest K Lee, Angelica Cibrian-Jaramillo, Sergios-Orestis Kolokotronis, Manpreet S Katari, Alexandros Stamatakis, Michael Ott, Joanna C Chiu, Damon P Little, Dennis Wm Stevenson, W Richard McCombie and 3 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
29.3field-weighted citation impact, top 1% 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

62 citing papers in PubMed, 152 citations in OpenAlex.

  1. Article
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  6. Model Species to Investigate the Origin of Flowers.Methods in molecular biology (Clifton, N.J.) · 2023
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  8. Plant ecological genomics at the limits of life in the Atacama Desert.Proceedings of the National Academy of Sciences of the United States of America · 2021
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  12. Phylogenomic conflict coincides with rapid morphological innovation.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  13. Article
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  16. A role forF1000Research · 2020
    Article
  17. Article
  18. Article
  19. Maternal small RNAs mediate spatial-temporal regulation of gene expression, imprinting, and seed development inProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  20. Article

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

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

13 authors at 7 institutions in 2 countries.

Ernest K LeeSackler Institute for Comparative Genomics, American Museum of Natural History, New York, New York, United States of America.
Angelica Cibrian-Jaramillo
Sergios-Orestis Kolokotronis
Manpreet S Katari
Alexandros Stamatakis
Michael Ott
Joanna C Chiu
Damon P Little
Dennis Wm Stevenson
W Richard McCombie
Robert A Martienssen
Gloria Coruzzi
Rob Desalle
American Museum of Natural History · USNew York Botanical Garden · USCold Spring Harbor Laboratory · USNew York University · USMunich University of Applied Sciences · DETechnical University of Munich · DEUniversity of California, Davis · US

Funding

Transposons, RNA Interference and HeterochromatinR01GM067014 · NIGMS · COLD SPRING HARBOR LABORATORY · PI MARTIENSSEN, ROBERT A · 2003 to 2016
$4.1M
NIGMS NIH HHS R01 GM067014
6 · The paper itself

Abstract

A novel result of the current research is the development and implementation of a unique functional phylogenomic approach that explores the genomic origins of seed plant diversification. We first use 22,833 sets of orthologs from the nuclear genomes of 101 genera across land plants to reconstruct their phylogenetic relationships. One of the more salient results is the resolution of some enigmatic relationships in seed plant phylogeny, such as the placement of Gnetales as sister to the rest of the gymnosperms. In using this novel phylogenomic approach, we were also able to identify overrepresented functional gene ontology categories in genes that provide positive branch support for major nodes prompting new hypotheses for genes associated with the diversification of angiosperms. For example, RNA interference (RNAi) has played a significant role in the divergence of monocots from other angiosperms, which has experimental support in Arabidopsis and rice. This analysis also implied that the second largest subunit of RNA polymerase IV and V (NRPD2) played a prominent role in the divergence of gymnosperms. This hypothesis is supported by the lack of 24nt siRNA in conifers, the maternal control of small RNA in the seeds of flowering plants, and the emergence of double fertilization in angiosperms. Our approach takes advantage of genomic data to define orthologs, reconstruct relationships, and narrow down candidate genes involved in plant evolution within a phylogenomic view of species' diversification.

Indexed as

Biological EvolutionGenome, PlantArabidopsisCycadopsidaDNA-Directed RNA PolymerasesEvolution, MolecularFlowersGenes, PlantGenomicsMagnoliopsidaOryzaPhylogenyPlantsRNA InterferenceRNA, Small InterferingSeedsDNA-Directed RNA PolymerasesRNA, Small Interfering

Identifiers

PMID22194700
PMCPMC3240601
OpenAlexW2079288754

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.