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The Swi3 protein plays a unique role in regulating respiration in eukaryotes
Recent experimental evidence increasingly shows that the dysregulation of cellular bioenergetics is associated with a wide array of common human diseases, including cancer, neurological diseases and diabetes. Respiration provides a vital source of cellular energy for most eukaryotic cells, particula...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293592/ https://www.ncbi.nlm.nih.gov/pubmed/27190130 http://dx.doi.org/10.1042/BSR20160083 |
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author | Lal, Sneha Alam, Md Maksudul Hooda, Jagmohan Shah, Ajit Cao, Thai M. Xuan, Zhenyu Zhang, Li |
author_facet | Lal, Sneha Alam, Md Maksudul Hooda, Jagmohan Shah, Ajit Cao, Thai M. Xuan, Zhenyu Zhang, Li |
author_sort | Lal, Sneha |
collection | PubMed |
description | Recent experimental evidence increasingly shows that the dysregulation of cellular bioenergetics is associated with a wide array of common human diseases, including cancer, neurological diseases and diabetes. Respiration provides a vital source of cellular energy for most eukaryotic cells, particularly high energy demanding cells. However, the understanding of how respiration is globally regulated is very limited. Interestingly, recent evidence suggests that Swi3 is an important regulator of respiration genes in yeast. In this report, we performed an array of biochemical and genetic experiments and computational analysis to directly evaluate the function of Swi3 and its human homologues in regulating respiration. First, we showed, by computational analysis and measurements of oxygen consumption and promoter activities, that Swi3, not Swi2, regulates genes encoding functions involved in respiration and oxygen consumption. Biochemical analysis showed that the levels of mitochondrial respiratory chain complexes were substantially increased in Δswi3 cells, compared with the parent cells. Additionally, our data showed that Swi3 strongly affects haem/oxygen-dependent activation of respiration gene promoters whereas Swi2 affects only the basal, haem-independent activities of these promoters. We found that increased expression of aerobic expression genes is correlated with increased oxygen consumption and growth rates in Δswi3 cells in air. Furthermore, using computational analysis and RNAi knockdown, we showed that the mammalian Swi3 BAF155 and BAF170 regulate respiration in HeLa cells. Together, these experimental and computational data demonstrated that Swi3 and its mammalian homologues are key regulators in regulating respiration. |
format | Online Article Text |
id | pubmed-5293592 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52935922017-02-14 The Swi3 protein plays a unique role in regulating respiration in eukaryotes Lal, Sneha Alam, Md Maksudul Hooda, Jagmohan Shah, Ajit Cao, Thai M. Xuan, Zhenyu Zhang, Li Biosci Rep Original Papers Recent experimental evidence increasingly shows that the dysregulation of cellular bioenergetics is associated with a wide array of common human diseases, including cancer, neurological diseases and diabetes. Respiration provides a vital source of cellular energy for most eukaryotic cells, particularly high energy demanding cells. However, the understanding of how respiration is globally regulated is very limited. Interestingly, recent evidence suggests that Swi3 is an important regulator of respiration genes in yeast. In this report, we performed an array of biochemical and genetic experiments and computational analysis to directly evaluate the function of Swi3 and its human homologues in regulating respiration. First, we showed, by computational analysis and measurements of oxygen consumption and promoter activities, that Swi3, not Swi2, regulates genes encoding functions involved in respiration and oxygen consumption. Biochemical analysis showed that the levels of mitochondrial respiratory chain complexes were substantially increased in Δswi3 cells, compared with the parent cells. Additionally, our data showed that Swi3 strongly affects haem/oxygen-dependent activation of respiration gene promoters whereas Swi2 affects only the basal, haem-independent activities of these promoters. We found that increased expression of aerobic expression genes is correlated with increased oxygen consumption and growth rates in Δswi3 cells in air. Furthermore, using computational analysis and RNAi knockdown, we showed that the mammalian Swi3 BAF155 and BAF170 regulate respiration in HeLa cells. Together, these experimental and computational data demonstrated that Swi3 and its mammalian homologues are key regulators in regulating respiration. Portland Press Ltd. 2016-06-30 /pmc/articles/PMC5293592/ /pubmed/27190130 http://dx.doi.org/10.1042/BSR20160083 Text en © 2016 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution Licence 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Papers Lal, Sneha Alam, Md Maksudul Hooda, Jagmohan Shah, Ajit Cao, Thai M. Xuan, Zhenyu Zhang, Li The Swi3 protein plays a unique role in regulating respiration in eukaryotes |
title | The Swi3 protein plays a unique role in regulating respiration in eukaryotes |
title_full | The Swi3 protein plays a unique role in regulating respiration in eukaryotes |
title_fullStr | The Swi3 protein plays a unique role in regulating respiration in eukaryotes |
title_full_unstemmed | The Swi3 protein plays a unique role in regulating respiration in eukaryotes |
title_short | The Swi3 protein plays a unique role in regulating respiration in eukaryotes |
title_sort | swi3 protein plays a unique role in regulating respiration in eukaryotes |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293592/ https://www.ncbi.nlm.nih.gov/pubmed/27190130 http://dx.doi.org/10.1042/BSR20160083 |
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