Evidence map›Paper›PMID 39627480›Full record

ArticleScientific reports2024

A fully automated morphological analysis of yeast mitochondria from wide-field fluorescence images.

Jana Vojtová, Martin Čapek, Sabrina Willeit, Tomáš Groušl, Věra Chvalová, Eva Kutejová, Vladimír Pevala, Leoš Shivaya Valášek, Mark Rinnerthaler

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 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.

Jana VojtováLaboratory of Regulation of Gene Expression, Institute of Microbiology of the Czech Academy of Sciences, Vídeňská 1083, Prague, 14220, Czech Republic. jana.vojtova@biomed.cas.cz.
Martin ČapekLight Microscopy, Institute of Molecular Genetics of the Czech Academy of Sciences, Prague, 14220, Czech Republic.
Sabrina WilleitBiosciences and Medical Biology, Paris-Lodron-University Salzburg, Hellbrunnerstrasse 34, Salzburg, 5020, Austria.
Tomáš GroušlLaboratory of Cell Signalling, Institute of Microbiology of the Czech Academy of Sciences, Prague, 14220, Czech Republic.
Věra ChvalováLaboratory of Cell Signalling, Institute of Microbiology of the Czech Academy of Sciences, Prague, 14220, Czech Republic.
Eva KutejováDepartment of Biochemistry and Protein Structure, Institute of Molecular Biology, Slovak Academy of Sciences, Bratislava, 84551, Slovakia.
Vladimír PevalaDepartment of Biochemistry and Protein Structure, Institute of Molecular Biology, Slovak Academy of Sciences, Bratislava, 84551, Slovakia.
Leoš Shivaya ValášekLaboratory of Regulation of Gene Expression, Institute of Microbiology of the Czech Academy of Sciences, Vídeňská 1083, Prague, 14220, Czech Republic.
Mark RinnerthalerBiosciences and Medical Biology, Paris-Lodron-University Salzburg, Hellbrunnerstrasse 34, Salzburg, 5020, Austria. mark.rinnerthaler@sbg.ac.at.

Funding

ERDF and MEYS CZ.02.01.01/00/22_008/0004575Interreg V-A Slovakia-Austria StruBioMol ITMS: 305011X666Ministry of Education, Youth, and Sports (Czech Republic) LUASK22100the Austrian Science Fund FWF P33511the Slovak Grant Agency VEGA 2/0069/23the Slovak Research and Development Agency SK-CZ-RD-21-0104
6 · The paper itself

Abstract

Mitochondrial morphology is an important parameter of cellular fitness. Although many approaches are available for assessing mitochondrial morphology in mammalian cells, only a few technically demanding and laborious methods are available for yeast cells. A robust, fully automated and user-friendly approach that would allow (1) segmentation of tubular and spherical mitochondria in the yeast Saccharomyces cerevisiae from conventional wide-field fluorescence images and (2) quantitative assessment of mitochondrial morphology is lacking. To address this, we compared Global thresholding segmentation with deep learning MitoSegNet segmentation, which we retrained on yeast cells. The deep learning model outperformed the Global thresholding segmentation. We applied it to segment mitochondria in strain lacking the MMI1/TMA19 gene encoding an ortholog of the human TCTP protein. Next, we performed a quantitative evaluation of segmented mitochondria by analyses available in ImageJ/Fiji and by MitoA analysis available in the MitoSegNet toolbox. By monitoring a wide range of morphological parameters, we described a novel mitochondrial phenotype of the mmi1Δ strain after its exposure to oxidative stress compared to that of the wild-type strain. The retrained deep learning model, all macros applied to run the analyses, as well as the detailed procedure are now available at https://github.com/LMCF-IMG/Morphology_Yeast_Mitochondria .

Indexed as

Image Processing, Computer-AssistedMitochondriaSaccharomyces cerevisiaeDeep LearningMicroscopy, FluorescenceOxidative StressSaccharomyces cerevisiae ProteinsSaccharomyces cerevisiae ProteinsDeep learningMitochondriaMmi1Oxidative stressTCTPYeast

Identifiers

PMID39627480
PMCPMC11615301

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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.