Nonsense-mediated mRNA decay of the ferric and cupric reductase mRNAs FRE1 and FRE2 in Saccharomyces cerevisiae
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Updated: Jan 22, 2026

Measurement of mRNA Decay Rates in Saccharomyces cerevisiae Using rpb1-1 Strains
Published on: December 13, 2014
Megan Peccarelli1, Taylor D Scott1, Bessie W Kebaara1
1Department of Biology, Baylor University, Waco, TX, USA.
Abstract:
The nonsense-mediated mRNA decay (NMD) pathway regulates mRNAs that aberrantly terminate translation. This includes aberrant mRNAs and functional natural mRNAs. Natural mRNA degradation by NMD is triggered by mRNA features and environmental cues. Saccharomyces cerevisiae encodes multiple proteins with ferric and cupric reductase activity. Here, we examined the regulation by NMD of two mRNAs, FRE1 and FRE2, encoding ferric and cupric reductases in S. cerevisiae. We found that FRE2 mRNAs are regulated by NMD under noninducing conditions and that the FRE2 3'-UTR contributes to the degradation of the mRNAs by NMD. Conversely, FRE1 mRNAs are not regulated by NMD under comparable conditions. These findings suggest that regulation of functionally related mRNAs by NMD can be differential and conditional.
Insights
The nonsense-mediated mRNA decay (NMD) pathway differentially regulates yeast mRNAs. NMD controls FRE2 mRNA levels, but not FRE1 mRNA, indicating conditional regulation of functionally related genes.
Area of Science:
- Molecular Biology
- Gene Regulation
- Yeast Genetics
Background:
- The nonsense-mediated mRNA decay (NMD) pathway is a crucial cellular surveillance mechanism that degrades aberrant and some functional mRNAs.
- NMD regulation is influenced by mRNA features and environmental signals, impacting gene expression.
- Saccharomyces cerevisiae possesses multiple reductase enzymes, including ferric and cupric reductases, encoded by genes like FRE1 and FRE2.
Purpose of the Study:
- To investigate the role of NMD in regulating the expression of FRE1 and FRE2 mRNAs in Saccharomyces cerevisiae.
- To determine if NMD-mediated regulation of these functionally related mRNAs is similar or distinct.
- To identify specific mRNA elements, such as the 3'-UTR, involved in NMD-mediated control.
Main Methods:
- Analysis of FRE1 and FRE2 mRNA levels under various conditions in Saccharomyces cerevisiae.
- Investigating the contribution of the FRE2 3'-untranslated region (3'-UTR) to mRNA stability.
- Utilizing genetic and molecular biology techniques to assess NMD pathway activity.
Main Results:
- FRE2 mRNA was found to be regulated by the NMD pathway under non-inducing conditions.
- The 3'-UTR of FRE2 mRNA was identified as a key element contributing to its NMD-mediated degradation.
- In contrast, FRE1 mRNA did not exhibit NMD-mediated regulation under similar experimental conditions.
Conclusions:
- NMD-mediated regulation of functionally related mRNAs can be both differential and conditional.
- The specific mRNA sequence and structure, particularly the 3'-UTR, dictate susceptibility to NMD.
- This study highlights the nuanced control of gene expression by mRNA decay pathways in yeast.
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