Radiation induces cell wall remodeling in Saccharomyces cerevisiae, identifying PIR1 as a potential marker.

IF 2.4
Nurdan Ozbek, Pinar Buket Thomas, Bilge Guvenc Tuna, Handan Tuncel
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Abstract

Purpose: Ionizing radiation is one of the main stressors inducing oxidative stress and genotoxic damage, leading to decreased cellular viability in addition to the activation of various stress response pathways. However, the impact of radiation on fungal cell wall integrity and its associated regulatory network remains poorly understood. The aim of this study was to investigate the effects of X-ray radiation on Saccharomyces cerevisiae on viability and the expression of key cell wall integrity genes.

Materials and methods: Wild-type Saccharomyces cerevisiae cells were grown to the late logarithmic phase (OD600 = 0.7-0.9) and then were exposed to 0 Gy, 25 Gy, or 50 Gy irradiation. Cell viability was evaluated by spotting and colony-forming unit (CFU) assays. Three independent radiation-related gene expression datasets were retrieved from publicly available databases, and common differentially expressed genes associated with cell wall integrity were determined. Selected targets were validated by real-time quantitative PCR (qPCR).

Results: Exposure to both 25 and 50 Gy radiation reduced survival and viability (25 Gy: 85.5 × 104 CFU/mL; 50 Gy: 46.0 × 104 CFU/mL) compared to non-irradiated control cells (103.2 × 104 CFU/mL). The apparent cell wall thickness in the 50 Gy-treated group, measured immediately and 1 hour after irradiation, was reduced compared to the non-irradiated control. A Gene Ontology-based integrative analysis across three independent radiation datasets identified PIR1 as the only shared gene associated with cell wall integrity. Subsequently, qPCR analysis revealed that FKS1 expression remained unchanged, whereas PIR1 expression was reduced in the 50 Gy radiation group compared to the control.

Conclusions: These findings support that the ionizing radiation not only affects cellular viability through intracellular damage but also alters cell wall architecture and its regulatory gene networks, potentially increasing susceptibility to irradiation stress.

辐射诱导酿酒酵母细胞壁重塑,鉴定PIR1为潜在的标记物。
目的:电离辐射是引起氧化应激和基因毒性损伤的主要应激源之一,除了激活多种应激反应途径外,还会导致细胞活力下降。然而,辐射对真菌细胞壁完整性及其相关调控网络的影响仍然知之甚少。本研究旨在探讨x射线辐照对酿酒酵母(Saccharomyces cerevisiae)细胞活力和细胞壁完整性关键基因表达的影响。材料与方法:将野生型酿酒酵母细胞培养至对数后期(OD600 = 0.7 ~ 0.9),分别接受0 Gy、25 Gy、50 Gy的辐照。通过斑点和集落形成单位(CFU)试验评估细胞活力。从公开可用的数据库中检索到三个独立的辐射相关基因表达数据集,并确定了与细胞壁完整性相关的常见差异表达基因。选择的靶点通过实时定量PCR (qPCR)进行验证。结果:与未受辐射的对照细胞(103.2 × 104 CFU/mL)相比,暴露于25 Gy和50 Gy的辐射降低了存活和活力(25 Gy: 85.5 × 104 CFU/mL; 50 Gy: 46.0 × 104 CFU/mL)。与未照射对照组相比,50 gy处理组在照射后立即和1小时测量的表观细胞壁厚度减少。一项基于基因本体论的综合分析横跨三个独立的辐射数据集,发现PIR1是唯一与细胞壁完整性相关的共享基因。随后,qPCR分析显示,与对照组相比,50 Gy辐射组的FKS1表达保持不变,而PIR1表达降低。结论:这些发现支持电离辐射不仅通过细胞内损伤影响细胞活力,而且改变细胞壁结构及其调控基因网络,潜在地增加对辐射胁迫的易感性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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