Evidence map›Paper›PMID 31442410›Full record

ArticleCell2019

A Species-Wide Inventory of NLR Genes and Alleles in Arabidopsis thaliana.

Anna-Lena Van de Weyer, Freddy Monteiro, Oliver J Furzer, Marc T Nishimura, Volkan Cevik, Kamil Witek, Jonathan D G Jones, Jeffery L Dangl, Detlef Weigel, Felix Bemm

Open access · hybridAbstract read
In one paragraph

Article in Cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 192 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
192citing papers in PubMed, 2 pooled it
64.5field-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

192 citing papers in PubMed, 2 syntheses or guidelines pooled it, 401 citations in OpenAlex.

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132 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

10 authors at 5 institutions in 4 countries.

Anna-Lena Van de WeyerDepartment of Molecular Biology, Max Planck Institute for Developmental Biology, 72076 Tübingen, Germany.
Freddy MonteiroHoward Hughes Medical Institute, Chevy Chase, MD 20815, USA; Department of Biology, University of North Carolina, Chapel Hill, NC 27599-3280, USA; Center for Research in Agricultural Genomics (CRAG), CSIC-IRTA-UAB-UB, 08193 Barcelona, Spain.
Oliver J FurzerHoward Hughes Medical Institute, Chevy Chase, MD 20815, USA; Department of Biology, University of North Carolina, Chapel Hill, NC 27599-3280, USA; The Sainsbury Laboratory, University of East Anglia, Norwich Research Park, Norwich NR4 7UH, UK.
Marc T NishimuraDepartment of Biology, Colorado State University, Fort Collins, CO 80523, USA.
Volkan CevikThe Sainsbury Laboratory, University of East Anglia, Norwich Research Park, Norwich NR4 7UH, UK; Milner Centre for Evolution & Department of Biology and Biochemistry, University of Bath, Bath BA2 7AY, UK.
Kamil WitekThe Sainsbury Laboratory, University of East Anglia, Norwich Research Park, Norwich NR4 7UH, UK.
Jonathan D G JonesThe Sainsbury Laboratory, University of East Anglia, Norwich Research Park, Norwich NR4 7UH, UK. Electronic address: jonathan.jones@tsl.ac.uk.
Jeffery L DanglHoward Hughes Medical Institute, Chevy Chase, MD 20815, USA. Electronic address: dangl@email.unc.edu.
Detlef WeigelDepartment of Molecular Biology, Max Planck Institute for Developmental Biology, 72076 Tübingen, Germany. Electronic address: weigel@weigelworld.org.
Felix BemmDepartment of Molecular Biology, Max Planck Institute for Developmental Biology, 72076 Tübingen, Germany.
University of East Anglia · GBMax Planck Institute for Developmental Biology · DEColorado State University · USHoward Hughes Medical Institute · USUniversity of North Carolina at Chapel Hill · US

Funding

Biotechnology and Biological Sciences Research Council BB/H019820/1Biotechnology and Biological Sciences Research Council BB/L009293/1Biotechnology and Biological Sciences Research Council BB/M003809/1Biotechnology and Biological Sciences Research Council BB/P021646/1Howard Hughes Medical Institute
6 · The paper itself

Abstract

Infectious disease is both a major force of selection in nature and a prime cause of yield loss in agriculture. In plants, disease resistance is often conferred by nucleotide-binding leucine-rich repeat (NLR) proteins, intracellular immune receptors that recognize pathogen proteins and their effects on the host. Consistent with extensive balancing and positive selection, NLRs are encoded by one of the most variable gene families in plants, but the true extent of intraspecific NLR diversity has been unclear. Here, we define a nearly complete species-wide pan-NLRome in Arabidopsis thaliana based on sequence enrichment and long-read sequencing. The pan-NLRome largely saturates with approximately 40 well-chosen wild strains, with half of the pan-NLRome being present in most accessions. We chart NLR architectural diversity, identify new architectures, and quantify selective forces that act on specific NLRs and NLR domains. Our study provides a blueprint for defining pan-NLRomes.

Indexed as

AllelesArabidopsisArabidopsis ProteinsDisease ResistanceGenetic VariationGenome, PlantNLR ProteinsPlant DiseasesPlant ImmunitySpecies SpecificityArabidopsis ProteinsNLR Proteinsdisease resistance genesgenomicsinnate immunityintegrated domainsNLRplant immunityRenSeqsequence captureSMRT sequencingtargeted enrichment

Identifiers

PMID31442410
PMCPMC6709784
OpenAlexW2969924257

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.