Evidence map›Paper›PMID 21619600›Full record

ArticleGenome biology2011

A physical map for the Amborella trichopoda genome sheds light on the evolution of angiosperm genome structure.

Andrea Zuccolo, John E Bowers, James C Estill, Zhiyong Xiong, Meizhong Luo, Aswathy Sebastian, José Luis Goicoechea, Kristi Collura, Yeisoo Yu, Yuannian Jiao and 21 more

Open access · goldAbstract read
In one paragraph

Article in Genome biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
6.1field-weighted citation impact, top 4% 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

15 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
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  3. Systematic evolution ofFrontiers in plant science · 2023
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  8. Water from the rock: Ancient aquatic angiosperms flow from the fossil record.Proceedings of the National Academy of Sciences of the United States of America · 2015
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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

31 authors at 9 institutions in 2 countries.

Andrea ZuccoloArizona Genomics Institute, School of Plant Sciences and BIO5 Institute for Collaborative Research, University of Arizona, 1657 East Helen Street, Tucson, AZ 85721, USA.
John E Bowers
James C Estill
Zhiyong Xiong
Meizhong Luo
Aswathy Sebastian
José Luis Goicoechea
Kristi Collura
Yeisoo Yu
Yuannian Jiao
Jill Duarte
Haibao Tang
Saravanaraj Ayyampalayam
Steve Rounsley
Dave Kudrna
Andrew H Paterson
J Chris Pires
Andre Chanderbali
Douglas E Soltis
Srikar Chamala
Brad Barbazuk
Pamela S Soltis
Victor A Albert
Hong Ma
Dina Mandoli
Jody Banks
John E Carlson
Jeffrey Tomkins
Claude W dePamphilis
Rod A Wing
Jim Leebens-Mack
University of Arizona · USUniversity of Georgia · USPennsylvania State University · USUniversity of Florida · USUniversity of Missouri · USClemson University · USFlorida Museum of Natural History · USPurdue University West Lafayette · USUniversity at Buffalo, State University of New York · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecent phylogenetic analyses have identified Amborella trichopoda, an understory tree species endemic to the forests of New Caledonia, as sister to a clade including all other known flowering plant species. The Amborella genome is a unique reference for understanding the evolution of angiosperm genomes because it can serve as an outgroup to root comparative analyses. A physical map, BAC end sequences and sample shotgun sequences provide a first view of the 870 Mbp Amborella genome.

resultsAnalysis of Amborella BAC ends sequenced from each contig suggests that the density of long terminal repeat retrotransposons is negatively correlated with that of protein coding genes. Syntenic, presumably ancestral, gene blocks were identified in comparisons of the Amborella BAC contigs and the sequenced Arabidopsis thaliana, Populus trichocarpa, Vitis vinifera and Oryza sativa genomes. Parsimony mapping of the loss of synteny corroborates previous analyses suggesting that the rate of structural change has been more rapid on lineages leading to Arabidopsis and Oryza compared with lineages leading to Populus and Vitis. The gamma paleohexiploidy event identified in the Arabidopsis, Populus and Vitis genomes is shown to have occurred after the divergence of all other known angiosperms from the lineage leading to Amborella.

conclusionsWhen placed in the context of a physical map, BAC end sequences representing just 5.4% of the Amborella genome have facilitated reconstruction of gene blocks that existed in the last common ancestor of all flowering plants. The Amborella genome is an invaluable reference for inferences concerning the ancestral angiosperm and subsequent genome evolution.

Indexed as

Evolution, MolecularGenome, PlantContig MappingDatabases, GeneticGenomicsMagnoliopsidaNew CaledoniaOpen Reading FramesPhylogenyPhylogeographyPloidiesRetroelementsSequence Analysis, DNASyntenyRetroelements

Identifiers

PMID21619600
PMCPMC3219971
OpenAlexW2122698216

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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.