Evidence map›Paper›PMID 24876251›Full record

ArticleThe Plant cell2014

Consequences of Whole-Genome Triplication as Revealed by Comparative Genomic Analyses of the Wild Radish Raphanus raphanistrum and Three Other Brassicaceae Species.

Gaurav D Moghe, David E Hufnagel, Haibao Tang, Yongli Xiao, Ian Dworkin, Christopher D Town, Jeffrey K Conner, Shin-Han Shiu

Open access · hybridAbstract read
In one paragraph

Article in The Plant cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
32.8field-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

61 citing papers in PubMed, 146 citations in OpenAlex.

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  18. Evolutionary analysis ofJournal of biosciences · 2021
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1 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

8 authors at 3 institutions in 1 country.

Gaurav D MoghePrograms in Genetics and Quantitative Biology, Michigan State University, East Lansing, Michigan 48824.
David E HufnagelDepartment of Plant Biology, Michigan State University, East Lansing, Michigan 48824.
Haibao TangJ. Craig Venter Institute, Rockville, Maryland 20850.
Yongli XiaoNational Institute of Allergy and Infectious Disease, National Institute of Health, Bethesda, Maryland 20892.
Ian DworkinDepartment of Zoology, Michigan State University, East Lansing, Michigan 48824.
Christopher D TownJ. Craig Venter Institute, Rockville, Maryland 20850.
Jeffrey K ConnerDepartment of Plant Biology, Michigan State University, East Lansing, Michigan 48824 Kellogg Biological Station, Michigan State University, East Lansing, Michigan 48824.
Shin-Han ShiuPrograms in Genetics and Quantitative Biology, Michigan State University, East Lansing, Michigan 48824 Department of Plant Biology, Michigan State University, East Lansing, Michigan 48824 shius@msu.edu.
Michigan State University · USJ. Craig Venter Institute · USNational Institute of Allergy and Infectious Diseases · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polyploidization events are frequent among flowering plants, and the duplicate genes produced via such events contribute significantly to plant evolution. We sequenced the genome of wild radish (Raphanus raphanistrum), a Brassicaceae species that experienced a whole-genome triplication event prior to diverging from Brassica rapa. Despite substantial gene gains in these two species compared with Arabidopsis thaliana and Arabidopsis lyrata, ∼70% of the orthologous groups experienced gene losses in R. raphanistrum and B. rapa, with most of the losses occurring prior to their divergence. The retained duplicates show substantial divergence in sequence and expression. Based on comparison of A. thaliana and R. raphanistrum ortholog floral expression levels, retained radish duplicates diverged primarily via maintenance of ancestral expression level in one copy and reduction of expression level in others. In addition, retained duplicates differed significantly from genes that reverted to singleton state in function, sequence composition, expression patterns, network connectivity, and rates of evolution. Using these properties, we established a statistical learning model for predicting whether a duplicate would be retained postpolyploidization. Overall, our study provides new insights into the processes of plant duplicate loss, retention, and functional divergence and highlights the need for further understanding factors controlling duplicate gene fate.

Identifiers

PMID24876251
PMCPMC4079359
OpenAlexW2172119655

What OpenQuestion holds

Textmetadata
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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.