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Characterization of the aodA, dnmA, mnSOD and pimA genes in Aspergillus nidulans

Mitochondria play key roles in cellular energy generation and lifespan of most eukaryotes. To understand the functions of four nuclear-encoded genes predicted to be related to the maintenance of mitochondrial morphology and function in Aspergillus nidulans, systematic characterization was carried ou...

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Autores principales: Leiter, Éva, Park, Hee-Soo, Kwon, Nak-Jung, Han, Kap-Hoon, Emri, Tamás, Oláh, Viktor, Mészáros, Ilona, Dienes, Beatrix, Vincze, János, Csernoch, László, Yu, Jae-Hyuk, Pócsi, István
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742808/
https://www.ncbi.nlm.nih.gov/pubmed/26846452
http://dx.doi.org/10.1038/srep20523
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author Leiter, Éva
Park, Hee-Soo
Kwon, Nak-Jung
Han, Kap-Hoon
Emri, Tamás
Oláh, Viktor
Mészáros, Ilona
Dienes, Beatrix
Vincze, János
Csernoch, László
Yu, Jae-Hyuk
Pócsi, István
author_facet Leiter, Éva
Park, Hee-Soo
Kwon, Nak-Jung
Han, Kap-Hoon
Emri, Tamás
Oláh, Viktor
Mészáros, Ilona
Dienes, Beatrix
Vincze, János
Csernoch, László
Yu, Jae-Hyuk
Pócsi, István
author_sort Leiter, Éva
collection PubMed
description Mitochondria play key roles in cellular energy generation and lifespan of most eukaryotes. To understand the functions of four nuclear-encoded genes predicted to be related to the maintenance of mitochondrial morphology and function in Aspergillus nidulans, systematic characterization was carried out. The deletion and overexpression mutants of aodA, dnmA, mnSOD and pimA encoding alternative oxidase, dynamin related protein, manganese superoxide dismutase and Lon protease, respectively, were generated and examined for their growth, stress tolerances, respiration, autolysis, cell death, sterigmatocystin production, hyphal morphology and size, and mitochondrial superoxide production as well as development. Overall, genetic manipulation of these genes had less effect on cellular physiology and ageing in A. nidulans than that of their homologs in another fungus Podospora anserina with a well-characterized senescence. The observed interspecial phenotypic differences can be explained by the dissimilar intrinsic stabilities of the mitochondrial genomes in A. nidulans and P. anserina. Furthermore, the marginally altered phenotypes observed in A. nidulans mutants indicate the presence of effective compensatory mechanisms for the complex networks of mitochondrial defense and quality control. Importantly, these findings can be useful for developing novel platforms for heterologous protein production, or on new biocontrol and bioremediation technologies based on Aspergillus species.
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spelling pubmed-47428082016-02-09 Characterization of the aodA, dnmA, mnSOD and pimA genes in Aspergillus nidulans Leiter, Éva Park, Hee-Soo Kwon, Nak-Jung Han, Kap-Hoon Emri, Tamás Oláh, Viktor Mészáros, Ilona Dienes, Beatrix Vincze, János Csernoch, László Yu, Jae-Hyuk Pócsi, István Sci Rep Article Mitochondria play key roles in cellular energy generation and lifespan of most eukaryotes. To understand the functions of four nuclear-encoded genes predicted to be related to the maintenance of mitochondrial morphology and function in Aspergillus nidulans, systematic characterization was carried out. The deletion and overexpression mutants of aodA, dnmA, mnSOD and pimA encoding alternative oxidase, dynamin related protein, manganese superoxide dismutase and Lon protease, respectively, were generated and examined for their growth, stress tolerances, respiration, autolysis, cell death, sterigmatocystin production, hyphal morphology and size, and mitochondrial superoxide production as well as development. Overall, genetic manipulation of these genes had less effect on cellular physiology and ageing in A. nidulans than that of their homologs in another fungus Podospora anserina with a well-characterized senescence. The observed interspecial phenotypic differences can be explained by the dissimilar intrinsic stabilities of the mitochondrial genomes in A. nidulans and P. anserina. Furthermore, the marginally altered phenotypes observed in A. nidulans mutants indicate the presence of effective compensatory mechanisms for the complex networks of mitochondrial defense and quality control. Importantly, these findings can be useful for developing novel platforms for heterologous protein production, or on new biocontrol and bioremediation technologies based on Aspergillus species. Nature Publishing Group 2016-02-05 /pmc/articles/PMC4742808/ /pubmed/26846452 http://dx.doi.org/10.1038/srep20523 Text en Copyright © 2016, Macmillan Publishers Limited 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 to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Leiter, Éva
Park, Hee-Soo
Kwon, Nak-Jung
Han, Kap-Hoon
Emri, Tamás
Oláh, Viktor
Mészáros, Ilona
Dienes, Beatrix
Vincze, János
Csernoch, László
Yu, Jae-Hyuk
Pócsi, István
Characterization of the aodA, dnmA, mnSOD and pimA genes in Aspergillus nidulans
title Characterization of the aodA, dnmA, mnSOD and pimA genes in Aspergillus nidulans
title_full Characterization of the aodA, dnmA, mnSOD and pimA genes in Aspergillus nidulans
title_fullStr Characterization of the aodA, dnmA, mnSOD and pimA genes in Aspergillus nidulans
title_full_unstemmed Characterization of the aodA, dnmA, mnSOD and pimA genes in Aspergillus nidulans
title_short Characterization of the aodA, dnmA, mnSOD and pimA genes in Aspergillus nidulans
title_sort characterization of the aoda, dnma, mnsod and pima genes in aspergillus nidulans
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742808/
https://www.ncbi.nlm.nih.gov/pubmed/26846452
http://dx.doi.org/10.1038/srep20523
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