Evidence map›Paper›PMID 27871090›Full record

ArticleNature2016

The genomic basis of circadian and circalunar timing adaptations in a midge.

Tobias S Kaiser, Birgit Poehn, David Szkiba, Marco Preussner, Fritz J Sedlazeck, Alexander Zrim, Tobias Neumann, Lam-Tung Nguyen, Andrea J Betancourt, Thomas Hummel and 5 more

Abstract read
In one paragraph

Article in Nature, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
–field-weighted citation impact
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

53 citing papers in PubMed.

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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.

Tobias S KaiserMax F. Perutz Laboratories, University of Vienna, Campus Vienna Biocenter, Dr. Bohr-Gasse 9/4, A-1030 Vienna, Austria.
Birgit PoehnMax F. Perutz Laboratories, University of Vienna, Campus Vienna Biocenter, Dr. Bohr-Gasse 9/4, A-1030 Vienna, Austria.
David SzkibaCenter for Integrative Bioinformatics Vienna, Max F. Perutz Laboratories, University of Vienna and Medical University of Vienna, Dr. Bohr-Gasse 9, A-1030 Vienna, Austria.
Marco PreussnerDepartment of Biology, Chemistry, Pharmacy, Institute of Chemistry and Biochemistry, FU Berlin, D-14195 Berlin, Germany.
Fritz J SedlazeckCenter for Integrative Bioinformatics Vienna, Max F. Perutz Laboratories, University of Vienna and Medical University of Vienna, Dr. Bohr-Gasse 9, A-1030 Vienna, Austria.
Alexander ZrimCenter for Integrative Bioinformatics Vienna, Max F. Perutz Laboratories, University of Vienna and Medical University of Vienna, Dr. Bohr-Gasse 9, A-1030 Vienna, Austria.
Tobias NeumannMax F. Perutz Laboratories, University of Vienna, Campus Vienna Biocenter, Dr. Bohr-Gasse 9/4, A-1030 Vienna, Austria.
Lam-Tung NguyenCenter for Integrative Bioinformatics Vienna, Max F. Perutz Laboratories, University of Vienna and Medical University of Vienna, Dr. Bohr-Gasse 9, A-1030 Vienna, Austria.
Andrea J BetancourtInstitute of Population Genetics, Department of Biomedical Sciences, University of Veterinary Medicine Vienna, Josef-Baumann-Gasse 1, A-1210 Vienna, Austria.
Thomas HummelResearch Platform 'Rhythms of Life', University of Vienna, A-1030 Vienna, Austria.
Heiko VogelDepartment of Entomology, Max Planck Institute for Chemical Ecology, Hans-Knöll-Straße 8, D-07745 Jena, Germany.
Silke DornerMax F. Perutz Laboratories, University of Vienna, Campus Vienna Biocenter, Dr. Bohr-Gasse 9/4, A-1030 Vienna, Austria.
Florian HeydDepartment of Biology, Chemistry, Pharmacy, Institute of Chemistry and Biochemistry, FU Berlin, D-14195 Berlin, Germany.
Arndt von HaeselerCenter for Integrative Bioinformatics Vienna, Max F. Perutz Laboratories, University of Vienna and Medical University of Vienna, Dr. Bohr-Gasse 9, A-1030 Vienna, Austria.
Kristin Tessmar-RaibleMax F. Perutz Laboratories, University of Vienna, Campus Vienna Biocenter, Dr. Bohr-Gasse 9/4, A-1030 Vienna, Austria.

Funding

Austrian Science Fund FWF Y 413European Research Council 337011
6 · The paper itself

Abstract

Organisms use endogenous clocks to anticipate regular environmental cycles, such as days and tides. Natural variants resulting in differently timed behaviour or physiology, known as chronotypes in humans, have not been well characterized at the molecular level. We sequenced the genome of Clunio marinus, a marine midge whose reproduction is timed by circadian and circalunar clocks. Midges from different locations show strain-specific genetic timing adaptations. We examined genetic variation in five C. marinus strains from different locations and mapped quantitative trait loci for circalunar and circadian chronotypes. The region most strongly associated with circadian chronotypes generates strain-specific differences in the abundance of calcium/calmodulin-dependent kinase II.1 (CaMKII.1) splice variants. As equivalent variants were shown to alter CaMKII activity in Drosophila melanogaster, and C. marinus (Cma)-CaMKII.1 increases the transcriptional activity of the dimer of the circadian proteins Cma-CLOCK and Cma-CYCLE, we suggest that modulation of alternative splicing is a mechanism for natural adaptation in circadian timing.

Indexed as

GenomicsTidal WavesAcclimatizationAlternative SplicingAnimalsCalcium-Calmodulin-Dependent Protein Kinase Type 2ChironomidaeCircadian ClocksCircadian RhythmCLOCK ProteinsDrosophila melanogasterGenetic Association StudiesGenetic VariationGenome, InsectMaleMoonCalcium-Calmodulin-Dependent Protein Kinase Type 2CLOCK Proteins

Identifiers

PMID27871090
PMCPMC5133387

What OpenQuestion holds

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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.