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Updated: Aug 30, 2026

Measurements of Physiological Stress Responses in C. Elegans
Published on: May 21, 2020
RNA-binding protein Csx1 mediates global control of gene expression in response to oxidative stress
Miguel A Rodríguez-Gabriel1, Gavin Burns, W Hayes McDonald
1Department of Molecular Biology, The Scripps Research Institute, La Jolla, CA 92037, USA. miguelr@scripps.edu
Abstract:
Fission yeast Spc1 (Sty1), a stress-activated mitogen-activated protein kinase (MAPK) homologous to human p38, orchestrates global changes in gene expression in response to diverse forms of cytotoxic stress. This control is partly mediated through Atf1, a transcription factor homologous to human ATF2. How Spc1 controls Atf1, and how the cells tailor gene expression patterns to different forms of stress, are unknown. Here we describe Csx1, a novel protein crucial for survival of oxidative but not osmotic stress. Csx1 associates with and stabilizes atf1+ mRNA in response to oxidative stress. Csx1 controls expression of the majority of the genes induced by oxidative stress, including most of the genes regulated by Spc1 and Atf1. These studies reveal a novel mechanism controlling MAPK-regulated transcription factors and suggest how gene expression patterns can be customized to specific forms of stress. Csx1-like proteins in humans may perform similar tasks.
Insights
A novel protein, Csx1, stabilizes mRNA for the Atf1 transcription factor during oxidative stress, controlling gene expression. This reveals a new mechanism for stress response customization in yeast and potentially humans.
Area of Science:
- Cellular Biology
- Molecular Biology
- Stress Response Mechanisms
Background:
- The Spc1 (Sty1) stress-activated MAPK pathway regulates gene expression in response to cytotoxic stress.
- This regulation involves the transcription factor Atf1, homologous to human ATF2.
- Mechanisms by which Spc1 controls Atf1 and how cells adapt gene expression to specific stresses remain unclear.
Purpose of the Study:
- To identify novel proteins involved in stress-activated MAPK signaling.
- To elucidate the mechanism by which Spc1 controls Atf1 activity.
- To understand how gene expression patterns are tailored to distinct stress types.
Main Methods:
- Characterization of a novel protein, Csx1, in fission yeast.
- Analysis of Csx1's role in oxidative and osmotic stress survival.
- Investigation of Csx1's association with atf1+ mRNA.
- Assessment of Csx1's impact on gene expression induced by oxidative stress.
Main Results:
- Csx1 is essential for survival under oxidative stress but not osmotic stress.
- Csx1 associates with and stabilizes atf1+ mRNA specifically during oxidative stress.
- Csx1 regulates the majority of genes induced by oxidative stress, including those controlled by Spc1 and Atf1.
Conclusions:
- Discovery of Csx1 as a novel protein crucial for oxidative stress response in fission yeast.
- Identification of a new mechanism for controlling MAPK-regulated transcription factors via mRNA stabilization.
- Implication that Csx1-like proteins in humans may play similar roles in stress adaptation.
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