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The ecl family gene ecl3(+) is induced by phosphate starvation and contributes to sexual differentiation in fission yeast
In Schizosaccharomyces pombe, ecl family genes are induced by several signals, such as starvation of various nutrients, including sulfur, amino acids and Mg(2+), and environmental stress, including heat or oxidative stress. These genes mediate appropriate cellular responses and contribute to the mai...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10038150/ https://www.ncbi.nlm.nih.gov/pubmed/36779416 http://dx.doi.org/10.1242/jcs.260759 |
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author | Ohtsuka, Hokuto Sakata, Hiroki Kitazaki, Yuto Tada, Masanobu Shimasaki, Takafumi Otsubo, Yoko Maekawa, Yasukichi Kobayashi, Mikuto Imada, Kazuki Yamashita, Akira Aiba, Hirofumi |
author_facet | Ohtsuka, Hokuto Sakata, Hiroki Kitazaki, Yuto Tada, Masanobu Shimasaki, Takafumi Otsubo, Yoko Maekawa, Yasukichi Kobayashi, Mikuto Imada, Kazuki Yamashita, Akira Aiba, Hirofumi |
author_sort | Ohtsuka, Hokuto |
collection | PubMed |
description | In Schizosaccharomyces pombe, ecl family genes are induced by several signals, such as starvation of various nutrients, including sulfur, amino acids and Mg(2+), and environmental stress, including heat or oxidative stress. These genes mediate appropriate cellular responses and contribute to the maintenance of cell viability and induction of sexual differentiation. Although this yeast has three ecl family genes with overlapping functions, any environmental conditions that induce ecl3(+) remain unidentified. We demonstrate that ecl3(+) is induced by phosphate starvation, similar to its chromosomally neighboring genes, pho1(+) and pho84(+), which respectively encode an extracellular acid phosphatase and an inorganic phosphate transporter. ecl3(+) expression was induced by the transcription factor Pho7 and affected by the cyclin-dependent kinase (CDK)-activating kinase Csk1. Phosphate starvation induced G1 arrest and sexual differentiation via ecl family genes. Biochemical analyses suggested that this G1 arrest was mediated by the stabilization of the CDK inhibitor Rum1, which was dependent on ecl family genes. This study shows that ecl family genes are required for appropriate responses to phosphate starvation and provides novel insights into the diversity and similarity of starvation responses. |
format | Online Article Text |
id | pubmed-10038150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-100381502023-03-25 The ecl family gene ecl3(+) is induced by phosphate starvation and contributes to sexual differentiation in fission yeast Ohtsuka, Hokuto Sakata, Hiroki Kitazaki, Yuto Tada, Masanobu Shimasaki, Takafumi Otsubo, Yoko Maekawa, Yasukichi Kobayashi, Mikuto Imada, Kazuki Yamashita, Akira Aiba, Hirofumi J Cell Sci Research Article In Schizosaccharomyces pombe, ecl family genes are induced by several signals, such as starvation of various nutrients, including sulfur, amino acids and Mg(2+), and environmental stress, including heat or oxidative stress. These genes mediate appropriate cellular responses and contribute to the maintenance of cell viability and induction of sexual differentiation. Although this yeast has three ecl family genes with overlapping functions, any environmental conditions that induce ecl3(+) remain unidentified. We demonstrate that ecl3(+) is induced by phosphate starvation, similar to its chromosomally neighboring genes, pho1(+) and pho84(+), which respectively encode an extracellular acid phosphatase and an inorganic phosphate transporter. ecl3(+) expression was induced by the transcription factor Pho7 and affected by the cyclin-dependent kinase (CDK)-activating kinase Csk1. Phosphate starvation induced G1 arrest and sexual differentiation via ecl family genes. Biochemical analyses suggested that this G1 arrest was mediated by the stabilization of the CDK inhibitor Rum1, which was dependent on ecl family genes. This study shows that ecl family genes are required for appropriate responses to phosphate starvation and provides novel insights into the diversity and similarity of starvation responses. The Company of Biologists Ltd 2023-03-10 /pmc/articles/PMC10038150/ /pubmed/36779416 http://dx.doi.org/10.1242/jcs.260759 Text en © 2023. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Ohtsuka, Hokuto Sakata, Hiroki Kitazaki, Yuto Tada, Masanobu Shimasaki, Takafumi Otsubo, Yoko Maekawa, Yasukichi Kobayashi, Mikuto Imada, Kazuki Yamashita, Akira Aiba, Hirofumi The ecl family gene ecl3(+) is induced by phosphate starvation and contributes to sexual differentiation in fission yeast |
title | The ecl family gene ecl3(+) is induced by phosphate starvation and contributes to sexual differentiation in fission yeast |
title_full | The ecl family gene ecl3(+) is induced by phosphate starvation and contributes to sexual differentiation in fission yeast |
title_fullStr | The ecl family gene ecl3(+) is induced by phosphate starvation and contributes to sexual differentiation in fission yeast |
title_full_unstemmed | The ecl family gene ecl3(+) is induced by phosphate starvation and contributes to sexual differentiation in fission yeast |
title_short | The ecl family gene ecl3(+) is induced by phosphate starvation and contributes to sexual differentiation in fission yeast |
title_sort | ecl family gene ecl3(+) is induced by phosphate starvation and contributes to sexual differentiation in fission yeast |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10038150/ https://www.ncbi.nlm.nih.gov/pubmed/36779416 http://dx.doi.org/10.1242/jcs.260759 |
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