Genome-wide identification of resistance genes and transcriptome regulation in yeast to accommodate ammonium toxicity

Abstract

Background: Ammonium is an important raw material for biomolecules and life activities, and the toxicity of ammonium is also an important ecological and agricultural issue. Ammonium toxicity in yeast has only recently been discovered, and information on its mechanism is limited. In recent years, environmental pollution caused by nitrogen-containing wastewater has been increasing. In addition, the use of yeast in bioreactors to produce nitrogen-containing compounds has been developed. Therefore, research on resistance mechanisms that allow yeast to grow under conditions of high concentrations of ammonium has become more and more important.

Results: To further understand the resistance mechanism of yeast to grow under high concentration of ammonium, we used NH₄Cl to screen a yeast non-essential gene-deletion library. We identified 61 NH₄Cl-sensitive deletion mutants from approximately 4200 mutants in the library, then 34 of them were confirmed by drop test analysis. Enrichment analysis of these 34 genes showed that biosynthesis metabolism, mitophagy, MAPK signaling, and other pathways may play important roles in NH₄Cl resistance. Transcriptome analysis under NH₄Cl stress revealed 451 significantly upregulated genes and 835 significantly downregulated genes. The genes are mainly enriched in: nitrogen compound metabolic process, cell wall, MAPK signaling pathway, mitophagy, and glycine, serine and threonine metabolism.

Conclusions: Our results present a broad view of biological pathways involved in the response to NH₄Cl stress, and thereby advance our understanding of the resistance genes and cellular transcriptional regulation under high concentration of ammonium.

Keywords: Ammonium; Genome-wide screen; NH4Cl; Saccharomyces cerevisiae; Transcriptome.