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Quantitative Live Cell Imaging of Nuclear Shape and Chromatin Dynamics During Development and Environmental Stress in Arabidopsis thaliana Root.

Journal of visualized experiments : JoVE · 5 Jun 2026 · 10.3791/71307

Abstract

The nucleus is the characteristic organelle of eukaryotic organisms. Unlike the classic textbook view of static nuclei, nuclear shape is dynamic in live cells. Altered or deformed nuclear shape is a hallmark of cancer in animal cells and environmental stress in plants. Nuclear envelope proteins interact with chromatin to regulate gene expression. Unfortunately, little is known about the impact of abiotic stress on nuclear shape, movement, and chromatin dynamics. To confront this issue, we developed a pipeline using confocal microscopy and particle tracking software to quantify nuclear and chromatin dynamics in Arabidopsis roots under control and abiotic stress condition. This confocal imaging method utilizes a dual fluorescently tagged marker line - nuclear envelope protein and chromatin - to perform live cell imaging of the root in model plant Arabidopsis thaliana under control and salt-stressed conditions. These captured movies are analyzed to quantify nuclear and chromatin dynamics using open-source image processing software Fiji/ImageJ with the help of the TrackMate plugin. To validate this method, we imaged and quantified chromatin movement in control and salt-stressed roots, revealing a decrease in chromatin speed under salt-stressed conditions. This method allows for quantitative live cell imaging of root nuclear shape and chromatin dynamics during plant development and environmental stress, thus enabling analysis of changes in nuclear and chromatin dynamics caused by abiotic stressors.

Plant phenotyping relevance

シロイヌナズナ根の核形状・クロマチン動態を定量する共焦点ライブイメージングと画像解析パイプラインを開発し、塩ストレス条件で検証しており、植物表現型取得が中心です。

abstractwe developed a pipeline using confocal microscopy and particle tracking software to quantify nuclear and chromatin dynamics in Arabidopsis roots under control and abiotic stress condition.
abstractTo validate this method, we imaged and quantified chromatin movement in control and salt-stressed roots

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