Evidence map›Paper›PMID 38738286›Full record

ArticleJournal of cell science2024

Multiscale chromatin dynamics and high entropy in plant iPSC ancestors.

Kinga Rutowicz, Joel Lüthi, Reinoud de Groot, René Holtackers, Yauhen Yakimovich, Diana M Pazmiño, Olivier Gandrillon, Lucas Pelkmans, Célia Baroux

Abstract read
In one paragraph

Article in Journal of cell science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Kinga RutowiczPlant Developmental Genetics, Institute of Plant and Microbial Biology, University of Zurich, 8008 Zurich, Switzerland.ORCID 0000-0003-4035-675X
Joel LüthiDepartment of Molecular Life Sciences, University of Zurich, 8050 Zurich, Switzerland.ORCID 0000-0003-3023-170X
Reinoud de GrootDepartment of Molecular Life Sciences, University of Zurich, 8050 Zurich, Switzerland.ORCID 0000-0002-1905-6501
René HoltackersDepartment of Molecular Life Sciences, University of Zurich, 8050 Zurich, Switzerland.
Yauhen YakimovichDepartment of Molecular Life Sciences, University of Zurich, 8050 Zurich, Switzerland.ORCID 0009-0000-2677-9858
Diana M PazmiñoPlant Developmental Genetics, Institute of Plant and Microbial Biology, University of Zurich, 8008 Zurich, Switzerland.ORCID 0009-0005-8499-8158
Olivier GandrillonLaboratory of Biology and Modeling of the Cell, University of Lyon, ENS de Lyon,69342 Lyon, France.ORCID 0000-0002-3676-6513
Lucas PelkmansDepartment of Molecular Life Sciences, University of Zurich, 8050 Zurich, Switzerland.ORCID 0000-0002-6754-9730
Célia BarouxPlant Developmental Genetics, Institute of Plant and Microbial Biology, University of Zurich, 8008 Zurich, Switzerland.ORCID 0000-0001-6307-2229

Funding

European Research Council ERC-2019-AdG-885579Swiss National Science Foundation 310030_185186University of Zurich K-74502-03-01
6 · The paper itself

Abstract

Plant protoplasts provide starting material for of inducing pluripotent cell masses that are competent for tissue regeneration in vitro, analogous to animal induced pluripotent stem cells (iPSCs). Dedifferentiation is associated with large-scale chromatin reorganisation and massive transcriptome reprogramming, characterised by stochastic gene expression. How this cellular variability reflects on chromatin organisation in individual cells and what factors influence chromatin transitions during culturing are largely unknown. Here, we used high-throughput imaging and a custom supervised image analysis protocol extracting over 100 chromatin features of cultured protoplasts. The analysis revealed rapid, multiscale dynamics of chromatin patterns with a trajectory that strongly depended on nutrient availability. Decreased abundance in H1 (linker histones) is hallmark of chromatin transitions. We measured a high heterogeneity of chromatin patterns indicating intrinsic entropy as a hallmark of the initial cultures. We further measured an entropy decline over time, and an antagonistic influence by external and intrinsic factors, such as phytohormones and epigenetic modifiers, respectively. Collectively, our study benchmarks an approach to understand the variability and evolution of chromatin patterns underlying plant cell reprogramming in vitro.

Indexed as

ChromatinEntropyInduced Pluripotent Stem CellsCellular ReprogrammingEpigenesis, GeneticHistonesPlant CellsProtoplastsChromatinHistonesArabidopsisChromatin dynamicsEntropyHigh-throughput imagingiPSCLinker histoneProtoplastSupervised image analysisTexture features

Identifiers

PMID38738286
PMCPMC11234377

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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.