Non-canonical chromatin-based functions for the threonine metabolic pathway

The emerging class of multi-functional proteins known as moonlighters challenges the "one protein, one function" mentality by demonstrating crosstalk between biological pathways that were previously thought to be functionally discrete. Here, we present new links between amino acid metabolism and chromatin regulation, two biological pathways that are critical for cellular and organismal homeostasis. We discovered that the threonine biosynthetic pathway is required for the transcriptional silencing of ribosomal DNA (rDNA) in Saccharomyces cerevisiae. The enzymes in the pathway promote rDNA silencing through distinct mechanisms as a subset of silencing phenotypes was rescued with exogenous threonine. In addition, we found that a key pathway enzyme, homoserine dehydrogenase, promotes DNA repair through a mechanism involving the MRX complex, a major player in DNA double strand break repair. These data further the understanding of enzymes with non-canonical roles, here demonstrated within the threonine biosynthetic pathway, and provide insight into their roles as potential anti-fungal pharmaceutical targets.

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Publication Details

Journal
Scientific Reports
Published
2024-09-30
DOI
https://doi.org/10.1038/s41598-024-72394-z
Primary Topic
DNA Repair Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

Non-canonical chromatin-based functions for the threonine metabolic pathway

Jennifer Chik, Stephen Klepin, Lorraine Pillus, Xue Bessie Su et al.
Scientific Reports
DNA Repair Mechanisms
article

Non-canonical chromatin-based functions for the threonine metabolic pathway

Jennifer Chik, Stephen Klepin, Lorraine Pillus, Xue Bessie Su, Jessica Raygoza
article en

Abstract

The emerging class of multi-functional proteins known as moonlighters challenges the "one protein, one function" mentality by demonstrating crosstalk between biological pathways that were previously thought to be functionally discrete. Here, we present new links between amino acid metabolism and chromatin regulation, two biological pathways that are critical for cellular and organismal homeostasis. We discovered that the threonine biosynthetic pathway is required for the transcriptional silencing of ribosomal DNA (rDNA) in Saccharomyces cerevisiae. The enzymes in the pathway promote rDNA silencing through distinct mechanisms as a subset of silencing phenotypes was rescued with exogenous threonine. In addition, we found that a key pathway enzyme, homoserine dehydrogenase, promotes DNA repair through a mechanism involving the MRX complex, a major player in DNA double strand break repair. These data further the understanding of enzymes with non-canonical roles, here demonstrated within the threonine biosynthetic pathway, and provide insight into their roles as potential anti-fungal pharmaceutical targets.

Scientific ReportsVol. 14(1)
University of California San Diego (US), MRC Laboratory for Molecular Cell Biology (GB), University College London (GB), Medical Research Council (GB)
National Science Foundation, National Institutes of Health, University of California, San Diego
Openalex Percentile: Top 85%
DNA Repair Mechanisms
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