GeneticsGeneticsPeer-reviewed journal article
Vir1p, the Yeast Homolog of Virilizer, is Required for mRNA m6A Methylation and Meiosis
Zachory M. ParkiD, Ethan BelnapiD, Matthew Remillard, Mark David RoseiD
Abstract
N6-Methyladenosine (m6A) is one of the most abundant modifications found on eukaryotic mRNAs. mRNA methylation regulates a host of biological processes including meiosis, a specialized diploid cell division program that results in the formation of haploid cells (gametes). During budding yeast meiosis, m6A levels peak early, before the initiation of the meiotic divisions. High-throughput studies and work from our lab showed that Ygl036wp, a previously uncharacterized protein interacts with Kar4p, a meiotic protein required for mRNA m6A-methylation. Ygl036wp has no discernable domains except for several intrinsically disordered regions. However, protein folding prediction tools showed that Ygl036wp folds like VIRMA/Virilizer/VIR, which is involved in mRNA m6A-methylation in higher eukaryotes. In addition, Ygl036wp has several conserved motifs shared with VIRMA/Virilizer/VIR proteins. Accordingly, we propose to call the gene VIR1 for budding yeast ortholog of VIRMA/Virilizer/VIR 1. In support, Vir1p interacts with all other members of the yeast methyltransferase complex and is required for mRNA m6A methylation and meiosis. Vir1p is required for the stability of proteins comprising the methyltransferase complex, suggesting that Vir1p acts as a scaffold to stabilize the complex. The vir1{Delta}/{Delta} mutant is defective for premeiotic S-phase, which is suppressed by overexpression of the early meiotic transcription factor IME1; additional overexpression of the translational regulator RIM4 is required for sporulation. Consistent with IME1 suppression, vir1{Delta}/{Delta} exhibits a defect in the abundance of IME1 mRNA, as well as transcripts within Ime1ps regulon. Suppression by IME1 revealed a defect in the expression of the middle meiotic transcription factor, Ndt80p (and genes in its regulon), which is rescued by additional overexpression of RIM4. Together, these data suggest that Vir1p is required for cells to initiate the meiotic program and for progression through the meiotic divisions and spore formation. Author SummaryYgl036wp is a previously uncharacterized protein that we propose to name Vir1p (budding yeast ortholog of VIRMA/Virilizer/VIR 1). Work from our lab and others initially found an interaction between Vir1p and members of the yeast mRNA methyltransferase complex (Kar4p and Mum2p). We found that Vir1p interacts with all known members of the methyltransferase complex and is required for mRNA methylation. Vir1p is required early in meiosis; vir1{Delta}/{Delta} mutants arrest due to the reduced expression of Ime1p. Lower levels of Ime1p cause severe disruption to the meiotic transcriptome in vir1{Delta}/{Delta}. The vir1{Delta}/{Delta} meiotic defect can be partially suppressed by the overexpression of IME1; full suppression requires overexpression of both IME1 and RIM4. Using recent advances in protein folding predictions, we found that Vir1p is a remote homolog of VIRMA/Virilizer/VIR and shares conserved motifs with the protein from other organisms. Vir1p, like VIRMA/Virilizer/VIR, stabilizes the methyltransferase complex.
- organism: yeast
- assay: metagenomics
- assay: proteomics
- research focus: cell type annotation
- research focus: gene regulatory network inference
- research focus: differential expression
- approach: statistical model
- approach: experimental assay
- Citations
- 12
- FWCI
- 1.07
- Field percentile
- top 27%
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