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Updated: Nov 9, 2025

Reconstitution of Msp1 Extraction Activity with Fully Purified Components
Published on: August 10, 2021
Dynamic post-transcriptional regulation by Mrn1 links cell wall homeostasis to mitochondrial structure and function
Kendra Reynaud1, Molly Brothers2, Michael Ly2
1California Institute for Quantitative Biosciences, University of California, Berkeley, Berkeley, California, United States of America.
Abstract:
The RNA-binding protein Mrn1 in Saccharomyces cerevisiae targets over 300 messenger RNAs, including many involved in cell wall biogenesis. The impact of Mrn1 on these target transcripts is not known, however, nor is the cellular role for this regulation. We have shown that Mrn1 represses target mRNAs through the action of its disordered, asparagine-rich amino-terminus. Its endogenous targets include the paralogous SUN domain proteins Nca3 and Uth1, which affect mitochondrial and cell wall structure and function. While loss of MRN1 has no effect on fermentative growth, we found that mrn1Δ yeast adapt more quickly to respiratory conditions. These cells also have enlarged mitochondria in fermentative conditions, mediated in part by dysregulation of NCA3, and this may explain their faster switch to respiration. Our analyses indicated that Mrn1 acts as a hub for integrating cell wall integrity and mitochondrial biosynthesis in a carbon-source responsive manner.
Insights
The RNA-binding protein Mrn1 regulates yeast cell wall and mitochondrial genes. Loss of Mrn1 enhances adaptation to respiratory conditions by altering mitochondrial structure.
Area of Science:
- Molecular Biology
- Yeast Genetics
- Cellular Respiration
Background:
- The RNA-binding protein Mrn1 in Saccharomyces cerevisiae regulates over 300 messenger RNAs.
- Mrn1's impact on target transcripts and its cellular role in regulation are not fully understood.
- Mrn1 targets include SUN domain proteins Nca3 and Uth1, affecting mitochondrial and cell wall functions.
Purpose of the Study:
- To investigate the regulatory impact of Mrn1 on its target mRNAs.
- To elucidate the cellular role of Mrn1-mediated gene regulation.
- To understand how Mrn1 integrates cell wall integrity and mitochondrial biosynthesis.
Main Methods:
- Analysis of Mrn1's N-terminal domain for regulatory function.
- Identification and study of endogenous Mrn1 targets, including Nca3 and Uth1.
- Phenotypic analysis of mrn1Δ yeast under fermentative and respiratory conditions.
Main Results:
- Mrn1 represses target mRNAs via its disordered, asparagine-rich amino-terminus.
- Loss of MRN1 leads to faster adaptation to respiratory conditions.
- mrn1Δ cells exhibit enlarged mitochondria under fermentative conditions, partly due to NCA3 dysregulation.
Conclusions:
- Mrn1 acts as a regulatory hub integrating cell wall integrity and mitochondrial biosynthesis.
- Mrn1-mediated regulation is responsive to carbon source availability.
- Dysregulation of Mrn1 affects mitochondrial morphology and respiratory adaptation in yeast.
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