Evidence map›Paper›PMID 30594127›Full record

ArticleBMC cell biology2018

Mitotic activity patterns and cytoskeletal changes throughout the progression of diapause developmental program in Daphnia.

Luxi Chen, Rosemary E Barnett, Martin Horstmann, Verena Bamberger, Lea Heberle, Nina Krebs, John K Colbourne, Rocío Gómez, Linda C Weiss

Abstract read
In one paragraph

Article in BMC cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 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

9 authors.

Luxi ChenDepartment of Animal Ecology, Evolution and Biodiversity, Ruhr-University Bochum, NDEF 05/751, Universitaetsstrasse 150, 44780, Bochum, Germany.
Rosemary E BarnettSchool of Biosciences, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.
Martin HorstmannDepartment of Animal Ecology, Evolution and Biodiversity, Ruhr-University Bochum, NDEF 05/751, Universitaetsstrasse 150, 44780, Bochum, Germany.
Verena BambergerDepartment of Animal Ecology, Evolution and Biodiversity, Ruhr-University Bochum, NDEF 05/751, Universitaetsstrasse 150, 44780, Bochum, Germany.
Lea HeberleDepartment of Animal Ecology, Evolution and Biodiversity, Ruhr-University Bochum, NDEF 05/751, Universitaetsstrasse 150, 44780, Bochum, Germany.
Nina KrebsDepartment of Animal Ecology, Evolution and Biodiversity, Ruhr-University Bochum, NDEF 05/751, Universitaetsstrasse 150, 44780, Bochum, Germany.
John K ColbourneSchool of Biosciences, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.
Rocío GómezDepartamento de Biología. Facultad de Ciencias, Universidad Autónoma de Madrid, 28049, Madrid, Spain.
Linda C WeissDepartment of Animal Ecology, Evolution and Biodiversity, Ruhr-University Bochum, NDEF 05/751, Universitaetsstrasse 150, 44780, Bochum, Germany. linda.weiss@rub.de.ORCID 0000-0002-7737-5017

Funding

Biotechnology and Biological Sciences Research Council
6 · The paper itself

Abstract

backgroundDiapause is a form of dormancy that is genetically predetermined to allow animals to overcome harsh environmental conditions. It is induced by predictive environmental cues bringing cellular activity levels into a state of suspended animation. Entering diapause requires organismal, molecular and cellular adaptation to severely reduced energy flows. Cells must therefore have evolved strategies that prepare them for periods with limited metabolic resources. However, changes that occur on the (sub-)cellular level have not been thoroughly described.

resultsWe investigated mitotic activity and we monitored cytoskeletal network changes in successive stages of diapausing and non-diapausing Daphnia magna embryos using (immuno-)fluorescent labeling. We find that embryos destined to diapause show a delayed and 2.5x slower mitotic activity in comparison to continuously developing embryos. Development is halted when D. magna embryos reach ~ 3500 cells, whereupon mitotic activity is absent and cytoskeletal components are severely reduced, rendering diapause cells compact and condensed.

conclusionIn the initiation phase of diapause, the slower cell division rate points to prolonged interphase duration, preparing the cells for diapause maintenance. During diapause, cytoskeletal depletion and cellular condensation may be a means to save energy resources. Our data provide insights into the sub-cellular change of diapause in Daphnia.

Indexed as

MitosisAnimalsCell CountCell NucleusCytoskeletonDaphniaDiapauseEmbryonic DevelopmentEmbryo, NonmammalianFemaleActinCytoskeletonDaphniaDiapauseDormancyEarly embryonic cell cycleEmbryo developmentTemperatureTubulin

Identifiers

PMID30594127
PMCPMC6310958

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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.