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Genomic analysis of the secretion stress response in the enzyme-producing cell factory Aspergillus niger

BACKGROUND: Filamentous fungi such as Aspergillus niger have a high capacity secretory system and are therefore widely exploited for the industrial production of native and heterologous proteins. However, in most cases the yields of non-fungal proteins are significantly lower than those obtained for...

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Autores principales: Guillemette, Thomas, van Peij, Noël NME, Goosen, Theo, Lanthaler, Karin, Robson, Geoffrey D, van den Hondel, Cees AMJJ, Stam, Hein, Archer, David B
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1894978/
https://www.ncbi.nlm.nih.gov/pubmed/17561995
http://dx.doi.org/10.1186/1471-2164-8-158
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author Guillemette, Thomas
van Peij, Noël NME
Goosen, Theo
Lanthaler, Karin
Robson, Geoffrey D
van den Hondel, Cees AMJJ
Stam, Hein
Archer, David B
author_facet Guillemette, Thomas
van Peij, Noël NME
Goosen, Theo
Lanthaler, Karin
Robson, Geoffrey D
van den Hondel, Cees AMJJ
Stam, Hein
Archer, David B
author_sort Guillemette, Thomas
collection PubMed
description BACKGROUND: Filamentous fungi such as Aspergillus niger have a high capacity secretory system and are therefore widely exploited for the industrial production of native and heterologous proteins. However, in most cases the yields of non-fungal proteins are significantly lower than those obtained for fungal proteins. One well-studied bottleneck appears to be the result of mis-folding of heterologous proteins in the ER during early stages of secretion, with related stress responses in the host, including the unfolded protein response (UPR). This study aims at uncovering transcriptional and translational responses occurring in A. niger exposed to secretion stress. RESULTS: A genome-wide transcriptional analysis of protein secretion-related stress responses was determined using Affymetrix DNA GeneChips and independent verification for selected genes. Endoplasmic reticulum (ER)-associated stress was induced either by chemical treatment of the wild-type cells with dithiothreitol (DTT) or tunicamycin, or by expressing a human protein, tissue plasminogen activator (t-PA). All of these treatments triggered the UPR, as shown by the expression levels of several well-known UPR target genes. The predicted proteins encoded by most of the up-regulated genes function as part of the secretory system including chaperones, foldases, glycosylation enzymes, vesicle transport proteins, and ER-associated degradation proteins. Several genes were down-regulated under stress conditions and these included several genes that encode secreted enzymes. Moreover, translational regulation under ER stress was investigated by polysomal fractionation. This analysis confirmed the post-transcriptional control of hacA expression and highlighted that differential translation also occurs during ER stress, in particular for some genes encoding secreted proteins or proteins involved in ribosomal biogenesis and assembly. CONCLUSION: This is first genome-wide analysis of both transcriptional and translational events following protein secretion stress. Insight has been gained into the molecular basis of protein secretion and secretion-related stress in an effective protein-secreting fungus, and provides an opportunity to identify target genes for manipulation in strain improvement strategies.
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spelling pubmed-18949782007-06-21 Genomic analysis of the secretion stress response in the enzyme-producing cell factory Aspergillus niger Guillemette, Thomas van Peij, Noël NME Goosen, Theo Lanthaler, Karin Robson, Geoffrey D van den Hondel, Cees AMJJ Stam, Hein Archer, David B BMC Genomics Research Article BACKGROUND: Filamentous fungi such as Aspergillus niger have a high capacity secretory system and are therefore widely exploited for the industrial production of native and heterologous proteins. However, in most cases the yields of non-fungal proteins are significantly lower than those obtained for fungal proteins. One well-studied bottleneck appears to be the result of mis-folding of heterologous proteins in the ER during early stages of secretion, with related stress responses in the host, including the unfolded protein response (UPR). This study aims at uncovering transcriptional and translational responses occurring in A. niger exposed to secretion stress. RESULTS: A genome-wide transcriptional analysis of protein secretion-related stress responses was determined using Affymetrix DNA GeneChips and independent verification for selected genes. Endoplasmic reticulum (ER)-associated stress was induced either by chemical treatment of the wild-type cells with dithiothreitol (DTT) or tunicamycin, or by expressing a human protein, tissue plasminogen activator (t-PA). All of these treatments triggered the UPR, as shown by the expression levels of several well-known UPR target genes. The predicted proteins encoded by most of the up-regulated genes function as part of the secretory system including chaperones, foldases, glycosylation enzymes, vesicle transport proteins, and ER-associated degradation proteins. Several genes were down-regulated under stress conditions and these included several genes that encode secreted enzymes. Moreover, translational regulation under ER stress was investigated by polysomal fractionation. This analysis confirmed the post-transcriptional control of hacA expression and highlighted that differential translation also occurs during ER stress, in particular for some genes encoding secreted proteins or proteins involved in ribosomal biogenesis and assembly. CONCLUSION: This is first genome-wide analysis of both transcriptional and translational events following protein secretion stress. Insight has been gained into the molecular basis of protein secretion and secretion-related stress in an effective protein-secreting fungus, and provides an opportunity to identify target genes for manipulation in strain improvement strategies. BioMed Central 2007-06-11 /pmc/articles/PMC1894978/ /pubmed/17561995 http://dx.doi.org/10.1186/1471-2164-8-158 Text en Copyright © 2007 Guillemette et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Guillemette, Thomas
van Peij, Noël NME
Goosen, Theo
Lanthaler, Karin
Robson, Geoffrey D
van den Hondel, Cees AMJJ
Stam, Hein
Archer, David B
Genomic analysis of the secretion stress response in the enzyme-producing cell factory Aspergillus niger
title Genomic analysis of the secretion stress response in the enzyme-producing cell factory Aspergillus niger
title_full Genomic analysis of the secretion stress response in the enzyme-producing cell factory Aspergillus niger
title_fullStr Genomic analysis of the secretion stress response in the enzyme-producing cell factory Aspergillus niger
title_full_unstemmed Genomic analysis of the secretion stress response in the enzyme-producing cell factory Aspergillus niger
title_short Genomic analysis of the secretion stress response in the enzyme-producing cell factory Aspergillus niger
title_sort genomic analysis of the secretion stress response in the enzyme-producing cell factory aspergillus niger
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1894978/
https://www.ncbi.nlm.nih.gov/pubmed/17561995
http://dx.doi.org/10.1186/1471-2164-8-158
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