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拟南芥根细胞类型中 RAD51 转录反应和细胞周期动态的差异揭示了对 DNA 损伤的敏感性不同。

Differences in RAD51 transcriptional response and cell cycle dynamics reveal varying sensitivity to DNA damage among Arabidopsis thaliana root cell types.

机构信息

Plant Biology Department, Swedish University of Agricultural Sciences, Almas allé 5, Uppsala, 756 51, Sweden.

Department of Biology, Institute of Molecular Plant Biology, Swiss Federal Institute of Technology Zürich, Zürich, 8092, Switzerland.

出版信息

New Phytol. 2024 Aug;243(3):966-980. doi: 10.1111/nph.19875. Epub 2024 Jun 6.

Abstract

Throughout their lifecycle, plants are subjected to DNA damage from various sources, both environmental and endogenous. Investigating the mechanisms of the DNA damage response (DDR) is essential to unravel how plants adapt to the changing environment, which can induce varying amounts of DNA damage. Using a combination of whole-mount single-molecule RNA fluorescence in situ hybridization (WM-smFISH) and plant cell cycle reporter lines, we investigated the transcriptional activation of a key homologous recombination (HR) gene, RAD51, in response to increasing amounts of DNA damage in Arabidopsis thaliana roots. The results uncover consistent variations in RAD51 transcriptional response and cell cycle arrest among distinct cell types and developmental zones. Furthermore, we demonstrate that DNA damage induced by genotoxic stress results in RAD51 transcription throughout the whole cell cycle, dissociating its traditional link with S/G2 phases. This work advances the current comprehension of DNA damage response in plants by demonstrating quantitative differences in DDR activation. In addition, it reveals new associations with the cell cycle and cell types, providing crucial insights for further studies of the broader response mechanisms in plants.

摘要

在其生命周期中,植物会受到来自环境和内源性的各种来源的 DNA 损伤。研究 DNA 损伤反应 (DDR) 的机制对于揭示植物如何适应不断变化的环境至关重要,因为这种变化会引起不同程度的 DNA 损伤。我们使用全胚原位单分子 RNA 荧光杂交 (WM-smFISH) 和植物细胞周期报告系的组合,研究了拟南芥根中 RAD51 这一关键同源重组 (HR) 基因在应对不断增加的 DNA 损伤时的转录激活情况。结果揭示了不同细胞类型和发育区中 RAD51 转录反应和细胞周期阻滞的一致变化。此外,我们证明了由遗传毒性应激引起的 DNA 损伤会导致 RAD51 在整个细胞周期中的转录,从而使其与 S/G2 期的传统联系分离。这项工作通过证明 DDR 激活的定量差异,推进了我们对植物中 DNA 损伤反应的理解。此外,它还揭示了与细胞周期和细胞类型的新关联,为进一步研究植物中更广泛的反应机制提供了关键见解。

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