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Kar4 is Required for the Normal Pattern of Meiotic Gene Expression
Zachory M Park1, Matthew Remillard2, Mark D Rose1,2
1Department of Biology, Georgetown University, Washington DC, 20057, USA.
Biorxiv : the Preprint Server for Biology
|February 7, 2023
Summary
Kar4p regulates meiosis through both transcriptional and translational mechanisms. Its loss causes defects in gene expression and protein levels, requiring co-overexpression of IME1 and RIM4 for full meiotic completion.
Area of Science:
- Molecular Biology
- Yeast Genetics
- Meiosis Regulation
Background:
- Kar4p, a yeast homolog of METTL14, is crucial for initiating meiosis.
- Kar4p exhibits dual functions, impacting both transcriptional and translational processes during meiosis.
- Loss of Kar4p leads to mRNA methylation defects and arrests the meiotic program.
Approach:
- Utilized microarray analysis and RNA sequencing to assess transcriptional profiles in kar4Δ/Δ mutants.
- Employed mass spectrometry to analyze protein levels of meiotic recombination genes.
- Investigated the effects of overexpressing IME1 and RIM4 on meiotic progression and gene expression.
Key Points:
- kar4Δ/Δ mutants display delayed and reduced expression of early (Ime1p-dependent) and late (Ndt80p-dependent) meiotic genes.
- Overexpression of IME1 rescues early gene expression defects, while late gene defects require co-overexpression of IME1 and RIM4.
- Reduced protein levels for meiotic recombination factors in kar4Δ/Δ mutants are rescued by co-overexpression of IME1 and RIM4, suggesting a non-catalytic function of Kar4p.
Conclusions:
- Kar4p plays essential roles in both transcriptional regulation and translational control during yeast meiosis.
- The meiotic defects in kar4Δ/Δ mutants, particularly for later meiotic events, are linked to translational regulation independent of mRNA methylation.
- Co-overexpression of IME1 and RIM4 is necessary to fully restore sporulation in the absence of Kar4p.
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