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Estimation of cell cycle kinetics in higher plant root meristem links organ position with cellular fate and chromatin structure

View ORCID ProfileTaras Pasternak, View ORCID ProfileStefan Kircher, Klaus Palme
doi: https://doi.org/10.1101/2021.01.01.425043
Taras Pasternak
1Faculty for Biology, Institute of Biology II/Molecular Plant Physiology
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  • For correspondence: taras.p.pasternak@gmail.com
Stefan Kircher
1Faculty for Biology, Institute of Biology II/Molecular Plant Physiology
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Klaus Palme
1Faculty for Biology, Institute of Biology II/Molecular Plant Physiology
2Centre for BioSystems Analysis, BIOSS Centre for Biological Signalling Studies; University of Freiburg, 79104 Freiburg, Germany
3State Key Laboratory of Crop Biology, College of Life Sciences, Shandong Agricultural University, Daizong Street 61, Tai’an, 271018, China
4Sino-German Joint Research Center on Agricultural Biology, College of Life Sciences, Shandong Agricultural University, Daizong Street 61, Tai’an, 271018, China
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Abstract

Plant root development is a complex spatial-temporal process that originates in the root apical meristem (RAM). To shape the organ’s structure signaling between the different cells and cell files must be highly coordinated. Thereby, diverging kinetics of chromatin remodeling and cell growth in these files need to be integrated and balanced by differential cell growth and local differences in cell proliferation frequency. Understanding the local differences in cell cycle duration in the RAM and its correlation with chromatin organization is crucial to build a holistic view on the different regulatory processes and requires a quantitative estimation of the chromatin geometry and underlying mitotic cell cycle phases’ timing at every cell file and every position. Unfortunately, so far precise methods for such analysis are missing.

This study presents a robust and straightforward pipeline to determine in parallel the duration of cell cycle’s key stages in all cell layers of a plant’s root and their nuclei organization. The methods combine marker-free techniques based on the detection of the nucleus, deep analysis of the chromatin phase transition, incorporation of 5-ethynyl-2′-deoxyuridine (EdU), and mitosis with a deep-resolution plant phenotyping platform to analyze all key cell cycle events’ kinetics.

In the Arabidopsis thaliana L. RAM S-phase duration was found to be as short as 20-30 minutes in all cell files. The subsequent G2-phase duration however depends on the cell type/position and varies from 3.5 hours in the pericycle to more than 4.5 hours in the epidermis. Overall, S+G2+M duration in Arabidopsis under our condition is 4 hours in the pericycle and up to 5.5 hours in the epidermis.

Endocycle duration was determined as the time required to achieve 100% EdU index in the transition zone and estimated to be in the range of 3-4 hours.

Besides Arabidopsis, we show that the presented technique is applicable also to root tips of other dicot and monocot plants (tobacco (Nicotiana tabacum L.), tomato (Lycopersicon esculentum L.) and wheat (Triticum aestivum L.).

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • This version of the manuscript has been revised to update the limk between cell size, nucleus size and cell cycle kinetics.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
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Posted June 13, 2021.
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Estimation of cell cycle kinetics in higher plant root meristem links organ position with cellular fate and chromatin structure
Taras Pasternak, Stefan Kircher, Klaus Palme
bioRxiv 2021.01.01.425043; doi: https://doi.org/10.1101/2021.01.01.425043
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Estimation of cell cycle kinetics in higher plant root meristem links organ position with cellular fate and chromatin structure
Taras Pasternak, Stefan Kircher, Klaus Palme
bioRxiv 2021.01.01.425043; doi: https://doi.org/10.1101/2021.01.01.425043

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