A novel transcription factor Sdr1 involving sulfur depletion response in fission yeast

Author:

Ohtsuka Hokuto1ORCID,Ohara Kotaro1,Shimasaki Takafumi1ORCID,Hatta Yoshiko1,Maekawa Yasukichi1,Aiba Hirofumi1ORCID

Affiliation:

1. Laboratory of Molecular Microbiology, Graduate School of Pharmaceutical Sciences Nagoya University Nagoya Japan

Abstract

AbstractIn the fission yeast Schizosaccharomyces pombe, the response to sulfur depletion has been less studied compared to the response to nitrogen depletion. Our study reveals that the fission yeast gene, SPCC417.09c, plays a significant role in the sulfur depletion response. This gene encodes a protein with a Zn2Cys6 fungal‐type DNA‐binding domain and a transcription factor domain, and we have named it sdr1+ (sulfur depletion response 1). Interestingly, while sulfur depletion typically induces autophagy akin to nitrogen depletion, we found that autophagy was not induced under sulfur depletion in the absence of sdr1+. This suggests that sdr1+ is necessary for the induction of autophagy under conditions of sulfur depletion. Although sdr1+ is not essential for the growth of fission yeast, its overexpression, driven by the nmt1 promoter, inhibits growth. This implies that Sdr1 may possess cell growth‐inhibitory capabilities. In addition, our analysis of Δsdr1 cells revealed that sdr1+ also plays a role in regulating the expression of genes associated with the phosphate depletion response. In conclusion, our study introduces Sdr1 as a novel transcription factor that contributes to an appropriate cellular nutrient starvation response. It does so by inhibiting inappropriate cell growth and inducing autophagy in response to sulfur depletion.

Funder

Japan Society for the Promotion of Science

Publisher

Wiley

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