Evidence map›Paper›PMID 30715408›Full record

ArticleMolecular biology and evolution2019

An Insect Counteradaptation against Host Plant Defenses Evolved through Concerted Neofunctionalization.

Hanna M Heidel-Fischer, Roy Kirsch, Michael Reichelt, Seung-Joon Ahn, Natalie Wielsch, Simon W Baxter, David G Heckel, Heiko Vogel, Juergen Kroymann

Open access · hybridAbstract read
In one paragraph

Article in Molecular biology and evolution, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

26 citing papers in PubMed, 67 citations in OpenAlex.

  1. Review
  2. Defense Responses of Cucumber and Cowpea toPlants (Basel, Switzerland) · 2026
    Article
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  10. New Insights into theJournal of agricultural and food chemistry · 2023
    Review
  11. Article
  12. International journal of molecular sciences · 2022
    Article
  13. Article
  14. Article
  15. Article
  16. Article
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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

9 authors at 4 institutions in 4 countries.

Hanna M Heidel-FischerDepartment of Entomology, Max Planck Institute for Chemical Ecology, Jena, Germany.
Roy KirschDepartment of Entomology, Max Planck Institute for Chemical Ecology, Jena, Germany.
Michael ReicheltDepartment of Biochemistry, Max Planck Institute for Chemical Ecology, Jena, Germany.
Seung-Joon AhnDepartment of Entomology, Max Planck Institute for Chemical Ecology, Jena, Germany.
Natalie WielschMass Spectrometry Group, Max Planck Institute for Chemical Ecology, Jena, Germany.
Simon W BaxterMolecular and Biomedical Science, School of Biological Sciences, University of Adelaide, Adelaide, Australia.
David G HeckelDepartment of Entomology, Max Planck Institute for Chemical Ecology, Jena, Germany.
Heiko VogelDepartment of Entomology, Max Planck Institute for Chemical Ecology, Jena, Germany.
Juergen KroymannGénétique et Écologie Évolutives, Écologie Systématique Evolution, CNRS/Université Paris-Sud/AgroParisTech, Université Paris-Saclay, Orsay Cedex, France.
Max Planck Institute for Chemical Ecology · DEOregon State University · USThe University of Adelaide · AUUniversité Paris-Sud · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antagonistic chemical interactions between herbivorous insects and their host plants are often thought to coevolve in a stepwise process, with an evolutionary innovation on one side being countered by a corresponding advance on the other. Glucosinolate sulfatase (GSS) enzyme activity is essential for the Diamondback moth, Plutella xylostella, to overcome a highly diversified secondary metabolite-based host defense system in the Brassicales. GSS genes are located in an ancient cluster of arylsulfataselike genes, but the exact roles of gene copies and their evolutionary trajectories are unknown. Here, we combine a functional investigation of duplicated insect arylsulfatases with an analysis of associated nucleotide substitution patterns. We show that the Diamondback moth genome encodes three GSSs with distinct substrate spectra and distinct expression patterns in response to glucosinolates. Contrary to our expectations, early functional diversification of gene copies was not indicative of a coevolutionary arms race between host and herbivore. Instead, both copies of a duplicated arylsulfatase gene evolved concertedly in the context of an insect host shift to acquire novel detoxifying functions under positive selection, a pattern of duplicate gene retention that we call "concerted neofunctionalization."

Indexed as

Biological CoevolutionHerbivoryAdaptation, BiologicalAnimalsFemaleGene DuplicationGenome, InsectGlucosinolatesInsect ProteinsMothsSulfatasesGlucosinolatesInsect ProteinsSulfataseschemical ecologycoevolutionary arms raceconcerted neofunctionalizationescape from adaptive conflictglucosinolate–myrosinase complexglucosinolate sulfataseinsect counteradaptationmolecular evolutionneofunctionalizationplant–insect interactionsPlutella xylostella

Identifiers

PMID30715408
PMCPMC6501874
OpenAlexW2912193322

What OpenQuestion holds

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LicenceCC BY
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.