Evidence map›Paper›PMID 28370647›Full record

ArticleMolecular ecology2017

Adaptive sequence evolution is driven by biotic stress in a pair of orchid species (Dactylorhiza) with distinct ecological optima.

Francisco Balao, Emiliano Trucchi, Thomas M Wolfe, Bao-Hai Hao, Maria Teresa Lorenzo, Juliane Baar, Laura Sedman, Carolin Kosiol, Fabian Amman, Mark W Chase and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular ecology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.1field-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

15 citing papers in PubMed, 30 citations in OpenAlex.

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  5. Speciation across the Earth driven by global cooling in terrestrial orchids.Proceedings of the National Academy of Sciences of the United States of America · 2023
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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

12 authors at 5 institutions in 6 countries.

Francisco BalaoDepartment of Botany and Biodiversity Research, University of Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0003-2104-3846
Emiliano TrucchiDepartment of Botany and Biodiversity Research, University of Vienna, Vienna, Austria.
Thomas M WolfeDepartment of Botany and Biodiversity Research, University of Vienna, Vienna, Austria.
Bao-Hai HaoDepartment of Botany and Biodiversity Research, University of Vienna, Vienna, Austria.
Maria Teresa LorenzoDepartment of Botany and Biodiversity Research, University of Vienna, Vienna, Austria.
Juliane BaarDepartment of Botany and Biodiversity Research, University of Vienna, Vienna, Austria.
Laura SedmanGregor Mendel Institute for Plant Molecular Biology, Vienna, Austria.
Carolin KosiolInstitut für Populationsgenetik, Vetmeduni Vienna, Vienna, Austria.
Fabian AmmanDepartment of Chromosome Biology, University of Vienna, Vienna, Austria.
Mark W ChaseRoyal Botanic Gardens Kew, Richmond, UK.
Mikael HedrénDepartment of Biology, Lund University, Lund, Sweden.
Ovidiu PaunDepartment of Botany and Biodiversity Research, University of Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0002-8295-4937
University of Vienna · ATGregor Mendel Institute of Molecular Plant Biology · ATLund University · SEThe University of Western Australia · AUUniversity of St Andrews · GB

Funding

Austrian Science Fund FWF W 1225Austrian Science Fund FWF Y 661
6 · The paper itself

Abstract

The orchid family is the largest in the angiosperms, but little is known about the molecular basis of the significant variation they exhibit. We investigate here the transcriptomic divergence between two European terrestrial orchids, Dactylorhiza incarnata and Dactylorhiza fuchsii, and integrate these results in the context of their distinct ecologies that we also document. Clear signals of lineage-specific adaptive evolution of protein-coding sequences are identified, notably targeting elements of biotic defence, including both physical and chemical adaptations in the context of divergent pools of pathogens and herbivores. In turn, a substantial regulatory divergence between the two species appears linked to adaptation/acclimation to abiotic conditions. Several of the pathways affected by differential expression are also targeted by deviating post-transcriptional regulation via sRNAs. Finally, D. incarnata appears to suffer from insufficient sRNA control over the activity of RNA-dependent DNA polymerase, resulting in increased activity of class I transposable elements and, over time, in larger genome size than that of D. fuchsii. The extensive molecular divergence between the two species suggests significant genomic and transcriptomic shock in their hybrids and offers insights into the difficulty of coexistence at the homoploid level. Altogether, biological response to selection, accumulated during the history of these orchids, appears governed by their microenvironmental context, in which biotic and abiotic pressures act synergistically to shape transcriptome structure, expression and regulation.

Indexed as

Biological EvolutionTranscriptomeAdaptation, BiologicalDNA Transposable ElementsEcologyEnvironmentGenome, PlantGenomicsOrchidaceaeDNA Transposable Elementsabiotic stressdefenceecological divergencepositive selectionsmall RNAstranscriptomics

Identifiers

PMID28370647
PMCPMC5518283
OpenAlexW2600453725

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.