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

被引:0
作者
Ohtsuka, Hokuto [1 ]
Ohara, Kotaro [1 ]
Shimasaki, Takafumi [1 ]
Hatta, Yoshiko [1 ]
Maekawa, Yasukichi [1 ]
Aiba, Hirofumi [1 ]
机构
[1] Nagoya Univ, Grad Sch Pharmaceut Sci, Lab Mol Microbiol, Chikusa Ku, Nagoya 4648601, Japan
基金
日本学术振兴会;
关键词
autophagy; Schizosaccharomyces pombe; sdr1(+) (sulfur depletion response 1); sulfur depletion; transcription factor; CHRONOLOGICAL LIFE-SPAN; GENE-EXPRESSION; DOWN-REGULATION; EXTENSION; ECL1;
D O I
10.1111/gtc.13136
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In 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 Zn(2)Cys(6) 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 Delta sdr1 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.
引用
收藏
页码:667 / 680
页数:14
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