Evidence map›Paper›PMID 28278261›Full record

ArticlePloS one2017

Evolutionary and biogeographical implications of degraded LAGLIDADG endonuclease functionality and group I intron occurrence in stony corals (Scleractinia) and mushroom corals (Corallimorpharia).

Juan Sebastián Celis, David R Edgell, Björn Stelbrink, Daniel Wibberg, Torsten Hauffe, Jochen Blom, Jörn Kalinowski, Thomas Wilke

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

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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

8 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
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  4. The Mitochondrial Genome of the Sea AnemoneLife (Basel, Switzerland) · 2021
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  5. The First Mitochondrial Genome ofFrontiers in fungal biology · 2021
    Article
  6. Article
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  8. Article
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 2 countries.

Juan Sebastián CelisAnimal Ecology and Systematics, Justus Liebig University, Giessen, Hessen, Germany.ORCID http://orcid.org/0000-0002-6800-4361
David R EdgellDepartment of Biochemistry, School of Medicine and Dentistry, Western University, London, Ontario, Canada.
Björn StelbrinkAnimal Ecology and Systematics, Justus Liebig University, Giessen, Hessen, Germany.
Daniel WibbergDepartment of Biochemistry, Institute for Genome Research and Systems Biology CeBiTec, Bielefeld University, Bielefeld, Germany.
Torsten HauffeAnimal Ecology and Systematics, Justus Liebig University, Giessen, Hessen, Germany.
Jochen BlomBioinformatics and Systems Biology, Justus Liebig University, Giessen, Germany.
Jörn KalinowskiDepartment of Biochemistry, Institute for Genome Research and Systems Biology CeBiTec, Bielefeld University, Bielefeld, Germany.
Thomas WilkeAnimal Ecology and Systematics, Justus Liebig University, Giessen, Hessen, Germany.
Justus-Liebig-Universität Gießen · DEBielefeld University · DEWestern University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Group I introns and homing endonuclease genes (HEGs) are mobile genetic elements, capable of invading target sequences in intron-less genomes. LAGLIDADG HEGs are the largest family of endonucleases, playing a key role in the mobility of group I introns in a process known as 'homing'. Group I introns and HEGs are rare in metazoans, and can be mainly found inserted in the COXI gene of some sponges and cnidarians, including stony corals (Scleractinia) and mushroom corals (Corallimorpharia). Vertical and horizontal intron transfer mechanisms have been proposed as explanations for intron occurrence in cnidarians. However, the central role of LAGLIDADG motifs in intron mobility mechanisms remains poorly understood. To resolve questions regarding the evolutionary origin and distribution of group I introns and HEGs in Scleractinia and Corallimorpharia, we examined intron/HEGs sequences within a comprehensive phylogenetic framework. Analyses of LAGLIDADG motif conservation showed a high degree of degradation in complex Scleractinia and Corallimorpharia. Moreover, the two motifs lack the respective acidic residues necessary for metal-ion binding and catalysis, potentially impairing horizontal intron mobility. In contrast, both motifs are highly conserved within robust Scleractinia, indicating a fully functional endonuclease capable of promoting horizontal intron transference. A higher rate of non-synonymous substitutions (Ka) detected in the HEGs of complex Scleractinia and Corallimorpharia suggests degradation of the HEG, whereas lower Ka rates in robust Scleractinia are consistent with a scenario of purifying selection. Molecular-clock analyses and ancestral inference of intron type indicated an earlier intron insertion in complex Scleractinia and Corallimorpharia in comparison to robust Scleractinia. These findings suggest that the lack of horizontal intron transfers in the former two groups is related to an age-dependent degradation of the endonuclease activity. Moreover, they also explain the peculiar geographical patterns of introns in stony and mushroom corals.

Indexed as

AgaricalesBiological EvolutionPhylogeographyAmino Acid SequenceAnimalsAnthozoaDNA, RibosomalEndonucleasesFungal ProteinsIntronsPhylogenyProteolysisSequence Analysis, DNASequence Homology, Amino AcidDNA, RibosomalEndonucleasesFungal Proteins

Identifiers

PMID28278261
PMCPMC5344465
OpenAlexW2593282124

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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.