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Light-inducible genetic engineering and control of non-homologous end-joining in industrial eukaryotic microorganisms: LML 3.0 and OFN 1.0

Filamentous fungi play important roles in the production of plant cell-wall degrading enzymes. In recent years, homologous recombinant technologies have contributed significantly to improved enzymes production and system design of genetically manipulated strains. When introducing multiple gene delet...

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Autores principales: Zhang, Lei, Zhao, Xihua, Zhang, Guoxiu, Zhang, Jiajia, Wang, Xuedong, Zhang, Suping, Wang, Wei, Wei, Dongzhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4746737/
https://www.ncbi.nlm.nih.gov/pubmed/26857594
http://dx.doi.org/10.1038/srep20761
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author Zhang, Lei
Zhao, Xihua
Zhang, Guoxiu
Zhang, Jiajia
Wang, Xuedong
Zhang, Suping
Wang, Wei
Wei, Dongzhi
author_facet Zhang, Lei
Zhao, Xihua
Zhang, Guoxiu
Zhang, Jiajia
Wang, Xuedong
Zhang, Suping
Wang, Wei
Wei, Dongzhi
author_sort Zhang, Lei
collection PubMed
description Filamentous fungi play important roles in the production of plant cell-wall degrading enzymes. In recent years, homologous recombinant technologies have contributed significantly to improved enzymes production and system design of genetically manipulated strains. When introducing multiple gene deletions, we need a robust and convenient way to control selectable marker genes, especially when only a limited number of markers are available in filamentous fungi. Integration after transformation is predominantly nonhomologous in most fungi other than yeast. Fungal strains deficient in the non-homologous end-joining (NHEJ) pathway have limitations associated with gene function analyses despite they are excellent recipient strains for gene targets. We describe strategies and methods to address these challenges above and leverage the power of resilient NHEJ deficiency strains. We have established a foolproof light-inducible platform for one-step unmarked genetic modification in industrial eukaryotic microorganisms designated as ‘LML 3.0’, and an on-off control protocol of NHEJ pathway called ‘OFN 1.0’, using a synthetic light-switchable transactivation to control Cre recombinase-based excision and inversion. The methods provide a one-step strategy to sequentially modify genes without introducing selectable markers and NHEJ-deficiency. The strategies can be used to manipulate many biological processes in a wide range of eukaryotic cells.
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spelling pubmed-47467372016-02-17 Light-inducible genetic engineering and control of non-homologous end-joining in industrial eukaryotic microorganisms: LML 3.0 and OFN 1.0 Zhang, Lei Zhao, Xihua Zhang, Guoxiu Zhang, Jiajia Wang, Xuedong Zhang, Suping Wang, Wei Wei, Dongzhi Sci Rep Article Filamentous fungi play important roles in the production of plant cell-wall degrading enzymes. In recent years, homologous recombinant technologies have contributed significantly to improved enzymes production and system design of genetically manipulated strains. When introducing multiple gene deletions, we need a robust and convenient way to control selectable marker genes, especially when only a limited number of markers are available in filamentous fungi. Integration after transformation is predominantly nonhomologous in most fungi other than yeast. Fungal strains deficient in the non-homologous end-joining (NHEJ) pathway have limitations associated with gene function analyses despite they are excellent recipient strains for gene targets. We describe strategies and methods to address these challenges above and leverage the power of resilient NHEJ deficiency strains. We have established a foolproof light-inducible platform for one-step unmarked genetic modification in industrial eukaryotic microorganisms designated as ‘LML 3.0’, and an on-off control protocol of NHEJ pathway called ‘OFN 1.0’, using a synthetic light-switchable transactivation to control Cre recombinase-based excision and inversion. The methods provide a one-step strategy to sequentially modify genes without introducing selectable markers and NHEJ-deficiency. The strategies can be used to manipulate many biological processes in a wide range of eukaryotic cells. Nature Publishing Group 2016-02-09 /pmc/articles/PMC4746737/ /pubmed/26857594 http://dx.doi.org/10.1038/srep20761 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
Zhang, Lei
Zhao, Xihua
Zhang, Guoxiu
Zhang, Jiajia
Wang, Xuedong
Zhang, Suping
Wang, Wei
Wei, Dongzhi
Light-inducible genetic engineering and control of non-homologous end-joining in industrial eukaryotic microorganisms: LML 3.0 and OFN 1.0
title Light-inducible genetic engineering and control of non-homologous end-joining in industrial eukaryotic microorganisms: LML 3.0 and OFN 1.0
title_full Light-inducible genetic engineering and control of non-homologous end-joining in industrial eukaryotic microorganisms: LML 3.0 and OFN 1.0
title_fullStr Light-inducible genetic engineering and control of non-homologous end-joining in industrial eukaryotic microorganisms: LML 3.0 and OFN 1.0
title_full_unstemmed Light-inducible genetic engineering and control of non-homologous end-joining in industrial eukaryotic microorganisms: LML 3.0 and OFN 1.0
title_short Light-inducible genetic engineering and control of non-homologous end-joining in industrial eukaryotic microorganisms: LML 3.0 and OFN 1.0
title_sort light-inducible genetic engineering and control of non-homologous end-joining in industrial eukaryotic microorganisms: lml 3.0 and ofn 1.0
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4746737/
https://www.ncbi.nlm.nih.gov/pubmed/26857594
http://dx.doi.org/10.1038/srep20761
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