Global Transcriptomic Analysis Identifies Gene Expression Programs Regulated by α-Factor in Yeast

In yeast, the mating pheromone α-factor triggers a signaling cascade in haploid "a" cells, leading to G1 cell cycle arrest, polarized growth ("shmoo" formation), cell wall remodeling, and ultimately cell fusion. While the physiological responses to α-factor are well established, a genome-wide analysis of transcriptional changes in response to α-factor has not been previously reported. Here, we performed RNA sequencing (RNA-seq) to profile gene expression changes in "a" mating type yeast cells treated with α-factor. We identified 957 differentially expressed genes (DEGs), including 448 upregulated and 509 downregulated genes. Gene ontology (GO) analysis revealed enrichment of upregulated genes in pheromone signaling, cell wall biogenesis, and cell shape regulation. In contrast, downregulated genes were mainly associated with cell cycle progression, chromatin remodeling, histone gene expression, and nucleosome organization. Our dataset validates known pheromone-responsive genes and identifies novel candidates potentially involved in mating responses. These findings provide a valuable resource for understanding how transcriptional regulation and chromatin dynamics are coordinated during pheromone signaling in yeast.

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Publication Details

Journal
Journal of Microbiology and Biotechnology
Published
2025-12-18
DOI
https://doi.org/10.4014/jmb.2509.09015
Primary Topic
Fungal and yeast genetics research
Type
article
Field-Weighted Citation Impact
0.00

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article

Global Transcriptomic Analysis Identifies Gene Expression Programs Regulated by α-Factor in Yeast

Jung-Shin Lee, Soojin Yeom
Journal of Microbiology and Biotechnology
Fungal and yeast genetics research
article

Global Transcriptomic Analysis Identifies Gene Expression Programs Regulated by α-Factor in Yeast

Jung-Shin Lee, Soojin Yeom
article en

Abstract

In yeast, the mating pheromone α-factor triggers a signaling cascade in haploid "a" cells, leading to G1 cell cycle arrest, polarized growth ("shmoo" formation), cell wall remodeling, and ultimately cell fusion. While the physiological responses to α-factor are well established, a genome-wide analysis of transcriptional changes in response to α-factor has not been previously reported. Here, we performed RNA sequencing (RNA-seq) to profile gene expression changes in "a" mating type yeast cells treated with α-factor. We identified 957 differentially expressed genes (DEGs), including 448 upregulated and 509 downregulated genes. Gene ontology (GO) analysis revealed enrichment of upregulated genes in pheromone signaling, cell wall biogenesis, and cell shape regulation. In contrast, downregulated genes were mainly associated with cell cycle progression, chromatin remodeling, histone gene expression, and nucleosome organization. Our dataset validates known pheromone-responsive genes and identifies novel candidates potentially involved in mating responses. These findings provide a valuable resource for understanding how transcriptional regulation and chromatin dynamics are coordinated during pheromone signaling in yeast.

Journal of Microbiology and BiotechnologyVol. 35
Kangwon National University (KR), Yonsei University (KR), Korea University (JP)
National Research Foundation, Kangwon National University, National Research Foundation of Korea, Ministry of Science and ICT, South Korea, Institute for Information and Communications Technology Promotion
Openalex Percentile: Top 37%
Fungal and yeast genetics research
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