Cargando…
The nucleolar protein nucleophosmin is essential for autophagy induced by inhibiting Pol I transcription
Various cellular stresses activate autophagy, which is involved in lysosomal degradation of cytoplasmic materials for maintaining nutrient homeostasis and eliminating harmful components. Here, we show that RNA polymerase I (Pol I) transcription inhibition induces nucleolar disruption and autophagy....
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4354046/ https://www.ncbi.nlm.nih.gov/pubmed/25754892 http://dx.doi.org/10.1038/srep08903 |
_version_ | 1782360693273526272 |
---|---|
author | Katagiri, Naohiro Kuroda, Takao Kishimoto, Hiroyuki Hayashi, Yuki Kumazawa, Takuya Kimura, Keiji |
author_facet | Katagiri, Naohiro Kuroda, Takao Kishimoto, Hiroyuki Hayashi, Yuki Kumazawa, Takuya Kimura, Keiji |
author_sort | Katagiri, Naohiro |
collection | PubMed |
description | Various cellular stresses activate autophagy, which is involved in lysosomal degradation of cytoplasmic materials for maintaining nutrient homeostasis and eliminating harmful components. Here, we show that RNA polymerase I (Pol I) transcription inhibition induces nucleolar disruption and autophagy. Treatment with autophagy inhibitors or siRNA specific for autophagy-related (ATG) proteins inhibited autophagy but not nucleolar disruption induced by Pol I transcription inhibition, which suggested that nucleolar disruption was upstream of autophagy. Furthermore, treatment with siRNA specific for nucleolar protein nucleophosmin (NPM) inhibited this type of autophagy. This showed that NPM was involved in autophagy when the nucleolus was disrupted by Pol I inhibition. In contrast, NPM was not required for canonical autophagy induced by nutrient starvation, as it was not accompanied by nucleolar disruption. Thus, our results revealed that, in addition to canonical autophagy, there may be NPM-dependent autophagy associated with nucleolar disruption. |
format | Online Article Text |
id | pubmed-4354046 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-43540462015-03-17 The nucleolar protein nucleophosmin is essential for autophagy induced by inhibiting Pol I transcription Katagiri, Naohiro Kuroda, Takao Kishimoto, Hiroyuki Hayashi, Yuki Kumazawa, Takuya Kimura, Keiji Sci Rep Article Various cellular stresses activate autophagy, which is involved in lysosomal degradation of cytoplasmic materials for maintaining nutrient homeostasis and eliminating harmful components. Here, we show that RNA polymerase I (Pol I) transcription inhibition induces nucleolar disruption and autophagy. Treatment with autophagy inhibitors or siRNA specific for autophagy-related (ATG) proteins inhibited autophagy but not nucleolar disruption induced by Pol I transcription inhibition, which suggested that nucleolar disruption was upstream of autophagy. Furthermore, treatment with siRNA specific for nucleolar protein nucleophosmin (NPM) inhibited this type of autophagy. This showed that NPM was involved in autophagy when the nucleolus was disrupted by Pol I inhibition. In contrast, NPM was not required for canonical autophagy induced by nutrient starvation, as it was not accompanied by nucleolar disruption. Thus, our results revealed that, in addition to canonical autophagy, there may be NPM-dependent autophagy associated with nucleolar disruption. Nature Publishing Group 2015-03-10 /pmc/articles/PMC4354046/ /pubmed/25754892 http://dx.doi.org/10.1038/srep08903 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Katagiri, Naohiro Kuroda, Takao Kishimoto, Hiroyuki Hayashi, Yuki Kumazawa, Takuya Kimura, Keiji The nucleolar protein nucleophosmin is essential for autophagy induced by inhibiting Pol I transcription |
title | The nucleolar protein nucleophosmin is essential for autophagy induced by inhibiting Pol I transcription |
title_full | The nucleolar protein nucleophosmin is essential for autophagy induced by inhibiting Pol I transcription |
title_fullStr | The nucleolar protein nucleophosmin is essential for autophagy induced by inhibiting Pol I transcription |
title_full_unstemmed | The nucleolar protein nucleophosmin is essential for autophagy induced by inhibiting Pol I transcription |
title_short | The nucleolar protein nucleophosmin is essential for autophagy induced by inhibiting Pol I transcription |
title_sort | nucleolar protein nucleophosmin is essential for autophagy induced by inhibiting pol i transcription |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4354046/ https://www.ncbi.nlm.nih.gov/pubmed/25754892 http://dx.doi.org/10.1038/srep08903 |
work_keys_str_mv | AT katagirinaohiro thenucleolarproteinnucleophosminisessentialforautophagyinducedbyinhibitingpolitranscription AT kurodatakao thenucleolarproteinnucleophosminisessentialforautophagyinducedbyinhibitingpolitranscription AT kishimotohiroyuki thenucleolarproteinnucleophosminisessentialforautophagyinducedbyinhibitingpolitranscription AT hayashiyuki thenucleolarproteinnucleophosminisessentialforautophagyinducedbyinhibitingpolitranscription AT kumazawatakuya thenucleolarproteinnucleophosminisessentialforautophagyinducedbyinhibitingpolitranscription AT kimurakeiji thenucleolarproteinnucleophosminisessentialforautophagyinducedbyinhibitingpolitranscription AT katagirinaohiro nucleolarproteinnucleophosminisessentialforautophagyinducedbyinhibitingpolitranscription AT kurodatakao nucleolarproteinnucleophosminisessentialforautophagyinducedbyinhibitingpolitranscription AT kishimotohiroyuki nucleolarproteinnucleophosminisessentialforautophagyinducedbyinhibitingpolitranscription AT hayashiyuki nucleolarproteinnucleophosminisessentialforautophagyinducedbyinhibitingpolitranscription AT kumazawatakuya nucleolarproteinnucleophosminisessentialforautophagyinducedbyinhibitingpolitranscription AT kimurakeiji nucleolarproteinnucleophosminisessentialforautophagyinducedbyinhibitingpolitranscription |