Evidence map›Paper›PMID 18842825›Full record

ArticlePlant physiology2008

Differential accumulation of retroelements and diversification of NB-LRR disease resistance genes in duplicated regions following polyploidy in the ancestor of soybean.

Roger W Innes, Carine Ameline-Torregrosa, Tom Ashfield, Ethalinda Cannon, Steven B Cannon, Ben Chacko, Nicolas W G Chen, Arnaud Couloux, Anita Dalwani, Roxanne Denny and 31 more

Open access · hybridAbstract read
In one paragraph

Article in Plant physiology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
14.7field-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

74 citing papers in PubMed, 146 citations in OpenAlex.

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14 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

41 authors at 6 institutions in 2 countries.

Roger W InnesDepartment of Biology, Indiana University, Bloomington, Indiana 47405, USA. rinnes@indiana.edu
Carine Ameline-Torregrosa
Tom Ashfield
Ethalinda Cannon
Steven B Cannon
Ben Chacko
Nicolas W G Chen
Arnaud Couloux
Anita Dalwani
Roxanne Denny
Shweta Deshpande
Ashley N Egan
Natasha Glover
Christian S Hans
Stacy Howell
Dan Ilut
Scott Jackson
Hongshing Lai
Jafar Mammadov
Sara Martin Del Campo
Michelle Metcalf
Ashley Nguyen
Majesta O'Bleness
Bernard E Pfeil
Ram Podicheti
Milind B Ratnaparkhe
Sylvie Samain
Iryna Sanders
Béatrice Ségurens
Mireille Sévignac
Sue Sherman-Broyles
Vincent Thareau
Dominic M Tucker
Jason Walling
Adam Wawrzynski
Jing Yi
Jeff J Doyle
Valérie Geffroy
Bruce A Roe
M A Saghai Maroof
Nevin D Young
Iowa State University · USIndiana University Bloomington · USUnited States Department of Agriculture · USUniversity of Minnesota · USUniversity of Missouri · USUniversity of Oklahoma · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The genomes of most, if not all, flowering plants have undergone whole genome duplication events during their evolution. The impact of such polyploidy events is poorly understood, as is the fate of most duplicated genes. We sequenced an approximately 1 million-bp region in soybean (Glycine max) centered on the Rpg1-b disease resistance gene and compared this region with a region duplicated 10 to 14 million years ago. These two regions were also compared with homologous regions in several related legume species (a second soybean genotype, Glycine tomentella, Phaseolus vulgaris, and Medicago truncatula), which enabled us to determine how each of the duplicated regions (homoeologues) in soybean has changed following polyploidy. The biggest change was in retroelement content, with homoeologue 2 having expanded to 3-fold the size of homoeologue 1. Despite this accumulation of retroelements, over 77% of the duplicated low-copy genes have been retained in the same order and appear to be functional. This finding contrasts with recent analyses of the maize (Zea mays) genome, in which only about one-third of duplicated genes appear to have been retained over a similar time period. Fluorescent in situ hybridization revealed that the homoeologue 2 region is located very near a centromere. Thus, pericentromeric localization, per se, does not result in a high rate of gene inactivation, despite greatly accelerated retrotransposon accumulation. In contrast to low-copy genes, nucleotide-binding-leucine-rich repeat disease resistance gene clusters have undergone dramatic species/homoeologue-specific duplications and losses, with some evidence for partitioning of subfamilies between homoeologues.

Indexed as

Evolution, MolecularGene DuplicationGenes, PlantPolyploidyRetroelementsCentromereChromosomes, Artificial, BacterialDNA, PlantGene DeletionGenome, PlantGlycine maxImmunity, InnateMultigene FamilyMutagenesis, InsertionalPhaseolusPhylogenyDNA, PlantRetroelements

Identifiers

PMID18842825
PMCPMC2593655
OpenAlexW1986939333

What OpenQuestion holds

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Read underepoch 390

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.