{"title":"裂变酵母中涉及硫耗竭反应的新型转录因子 Sdr1","authors":"Hokuto Ohtsuka, Kotaro Ohara, Takafumi Shimasaki, Yoshiko Hatta, Yasukichi Maekawa, Hirofumi Aiba","doi":"10.1111/gtc.13136","DOIUrl":null,"url":null,"abstract":"<p>In the fission yeast <i>Schizosaccharomyces pombe</i>, 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<sub>2</sub>Cys<sub>6</sub> fungal-type DNA-binding domain and a transcription factor domain, and we have named it <i>sdr1</i><sup>+</sup> (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 <i>sdr1</i><sup>+</sup>. This suggests that <i>sdr1</i><sup>+</sup> is necessary for the induction of autophagy under conditions of sulfur depletion. Although <i>sdr1</i><sup>+</sup> is not essential for the growth of fission yeast, its overexpression, driven by the <i>nmt1</i> promoter, inhibits growth. This implies that Sdr1 may possess cell growth-inhibitory capabilities. In addition, our analysis of Δ<i>sdr1</i> cells revealed that <i>sdr1</i><sup>+</sup> 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.</p>","PeriodicalId":12742,"journal":{"name":"Genes to Cells","volume":"29 8","pages":"667-680"},"PeriodicalIF":1.3000,"publicationDate":"2024-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A novel transcription factor Sdr1 involving sulfur depletion response in fission yeast\",\"authors\":\"Hokuto Ohtsuka, Kotaro Ohara, Takafumi Shimasaki, Yoshiko Hatta, Yasukichi Maekawa, Hirofumi Aiba\",\"doi\":\"10.1111/gtc.13136\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>In the fission yeast <i>Schizosaccharomyces pombe</i>, 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<sub>2</sub>Cys<sub>6</sub> fungal-type DNA-binding domain and a transcription factor domain, and we have named it <i>sdr1</i><sup>+</sup> (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 <i>sdr1</i><sup>+</sup>. This suggests that <i>sdr1</i><sup>+</sup> is necessary for the induction of autophagy under conditions of sulfur depletion. Although <i>sdr1</i><sup>+</sup> is not essential for the growth of fission yeast, its overexpression, driven by the <i>nmt1</i> promoter, inhibits growth. This implies that Sdr1 may possess cell growth-inhibitory capabilities. In addition, our analysis of Δ<i>sdr1</i> cells revealed that <i>sdr1</i><sup>+</sup> 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.</p>\",\"PeriodicalId\":12742,\"journal\":{\"name\":\"Genes to Cells\",\"volume\":\"29 8\",\"pages\":\"667-680\"},\"PeriodicalIF\":1.3000,\"publicationDate\":\"2024-06-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Genes to Cells\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/gtc.13136\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genes to Cells","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/gtc.13136","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
A novel transcription factor Sdr1 involving sulfur depletion response in fission yeast
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 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.
期刊介绍:
Genes to Cells provides an international forum for the publication of papers describing important aspects of molecular and cellular biology. The journal aims to present papers that provide conceptual advance in the relevant field. Particular emphasis will be placed on work aimed at understanding the basic mechanisms underlying biological events.