Evidence map›Paper›PMID 26201466›Full record

ArticleGenome biology2015

Kiwi genome provides insights into evolution of a nocturnal lifestyle.

Diana Le Duc, Gabriel Renaud, Arunkumar Krishnan, Markus Sällman Almén, Leon Huynen, Sonja J Prohaska, Matthias Ongyerth, Bárbara D Bitarello, Helgi B Schiöth, Michael Hofreiter and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Genome biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
10.9field-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

36 citing papers in PubMed, 101 citations in OpenAlex.

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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

15 authors at 7 institutions in 4 countries.

Diana Le DucInstitute of Biochemistry, Medical Faculty, University of Leipzig, Johannisallee 30, Leipzig, 04103, Germany. diana_leduc@eva.mpg.de.
Gabriel RenaudDepartment of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology, Leipzig, 04103, Germany. gabriel_renaud@eva.mpg.de.
Arunkumar KrishnanDepartment of Neuroscience, Unit of Functional Pharmacology, Uppsala University, Box 593, Husargatan 3, Uppsala, 751 24, Sweden. arunkumar.krishnan@neuro.uu.se.
Markus Sällman AlménDepartment of Neuroscience, Unit of Functional Pharmacology, Uppsala University, Box 593, Husargatan 3, Uppsala, 751 24, Sweden. markus.sallman-almen@neuro.uu.se.
Leon HuynenGriffith School of Environment and School of Biomolecular and Physical Sciences, Griffith University, Nathan, Queensland, 4111, Australia. l.huynen@griffith.edu.au.
Sonja J ProhaskaDepartment of Computer Science, and Interdisciplinary Center for Bioinformatics, University of Leipzig, Leipzig, 04103, Germany. sonja@bioinf.uni-leipzig.de.
Matthias OngyerthDepartment of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology, Leipzig, 04103, Germany. matthias_ongyerth@eva.mpg.de.
Bárbara D BitarelloDepartment of Genetics and Evolutionary Biology, University of São Paulo, São Paulo, SP, 05508-090, Brazil. barbarabitarello@gmail.com.
Helgi B SchiöthDepartment of Neuroscience, Unit of Functional Pharmacology, Uppsala University, Box 593, Husargatan 3, Uppsala, 751 24, Sweden. helgi.schioth@neuro.uu.se.
Michael HofreiterAdaptive Evolutionary Genomics, Institute for Biochemistry and Biology, University Potsdam, Potsdam, 14469, Germany. michi@palaeo.eu.
Peter F StadlerDepartment of Computer Science, and Interdisciplinary Center for Bioinformatics, University of Leipzig, Leipzig, 04103, Germany. studla@bioinf.uni-leipzig.de.
Kay PrüferDepartment of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology, Leipzig, 04103, Germany. pruefer@eva.mpg.de.
David LambertGriffith School of Environment and School of Biomolecular and Physical Sciences, Griffith University, Nathan, Queensland, 4111, Australia. d.lambert@griffith.edu.au.
Janet KelsoDepartment of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology, Leipzig, 04103, Germany. kelso@eva.mpg.de.
Torsten SchönebergInstitute of Biochemistry, Medical Faculty, University of Leipzig, Johannisallee 30, Leipzig, 04103, Germany. schoberg@medizin.uni-leipzig.de.
Max Planck Institute for Evolutionary Anthropology · DEUppsala University · SEGriffith University · AULeipzig University · DELeipzig University of Applied Sciences · DEUniversidade de São Paulo · BRUniversity of Potsdam · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundKiwi, comprising five species from the genus Apteryx, are endangered, ground-dwelling bird species endemic to New Zealand. They are the smallest and only nocturnal representatives of the ratites. The timing of kiwi adaptation to a nocturnal niche and the genomic innovations, which shaped sensory systems and morphology to allow this adaptation, are not yet fully understood.

resultsWe sequenced and assembled the brown kiwi genome to 150-fold coverage and annotated the genome using kiwi transcript data and non-redundant protein information from multiple bird species. We identified evolutionary sequence changes that underlie adaptation to nocturnality and estimated the onset time of these adaptations. Several opsin genes involved in color vision are inactivated in the kiwi. We date this inactivation to the Oligocene epoch, likely after the arrival of the ancestor of modern kiwi in New Zealand. Genome comparisons between kiwi and representatives of ratites, Galloanserae, and Neoaves, including nocturnal and song birds, show diversification of kiwi's odorant receptors repertoire, which may reflect an increased reliance on olfaction rather than sight during foraging. Further, there is an enrichment of genes influencing mitochondrial function and energy expenditure among genes that are rapidly evolving specifically on the kiwi branch, which may also be linked to its nocturnal lifestyle.

conclusionsThe genomic changes in kiwi vision and olfaction are consistent with changes that are hypothesized to occur during adaptation to nocturnal lifestyle in mammals. The kiwi genome provides a valuable genomic resource for future genome-wide comparative analyses to other extinct and extant diurnal ratites.

Indexed as

DarknessEvolution, MolecularGenomeAdaptation, BiologicalAnimalsGenomicsMolecular Sequence AnnotationMolecular Sequence DataMultigene FamilyPalaeognathaeSelection, GeneticSmellVision, Ocular

Identifiers

PMID26201466
PMCPMC4511969
OpenAlexW1626178800

What OpenQuestion holds

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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.