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Identification and functional analysis of beta-tubulin genes by site specific integrative transformation in Aspergillus nidulans

We have cloned two different beta-tubulin sequences from the filamentous fungus Aspergillus nidulans. Each was used in the construction of transforming plasmids that carry the pyr4 gene of Neurospora crassa. We used these plasmids to transform a pyrG-strain of Aspergillus to uridine prototrophy. Bot...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1985
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2113715/
https://www.ncbi.nlm.nih.gov/pubmed/3897247
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description We have cloned two different beta-tubulin sequences from the filamentous fungus Aspergillus nidulans. Each was used in the construction of transforming plasmids that carry the pyr4 gene of Neurospora crassa. We used these plasmids to transform a pyrG-strain of Aspergillus to uridine prototrophy. Both plasmids were shown to integrate site specifically into the homologous chromosomal sequences. We then used transformant strains in genetic crosses to demonstrate that one of the cloned beta-tubulin sequences was the benA beta-tubulin gene, which codes for the beta 1-and beta 2-tubulins. The other cloned beta-tubulin sequence was shown to be the structural gene for beta 3- tubulin by gene disruption and to participate in conidial development. This is the first report of a gene disruption by site specific, integrative recombination in Aspergillus nidulans.
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spelling pubmed-21137152008-05-01 Identification and functional analysis of beta-tubulin genes by site specific integrative transformation in Aspergillus nidulans J Cell Biol Articles We have cloned two different beta-tubulin sequences from the filamentous fungus Aspergillus nidulans. Each was used in the construction of transforming plasmids that carry the pyr4 gene of Neurospora crassa. We used these plasmids to transform a pyrG-strain of Aspergillus to uridine prototrophy. Both plasmids were shown to integrate site specifically into the homologous chromosomal sequences. We then used transformant strains in genetic crosses to demonstrate that one of the cloned beta-tubulin sequences was the benA beta-tubulin gene, which codes for the beta 1-and beta 2-tubulins. The other cloned beta-tubulin sequence was shown to be the structural gene for beta 3- tubulin by gene disruption and to participate in conidial development. This is the first report of a gene disruption by site specific, integrative recombination in Aspergillus nidulans. The Rockefeller University Press 1985-09-01 /pmc/articles/PMC2113715/ /pubmed/3897247 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Identification and functional analysis of beta-tubulin genes by site specific integrative transformation in Aspergillus nidulans
title Identification and functional analysis of beta-tubulin genes by site specific integrative transformation in Aspergillus nidulans
title_full Identification and functional analysis of beta-tubulin genes by site specific integrative transformation in Aspergillus nidulans
title_fullStr Identification and functional analysis of beta-tubulin genes by site specific integrative transformation in Aspergillus nidulans
title_full_unstemmed Identification and functional analysis of beta-tubulin genes by site specific integrative transformation in Aspergillus nidulans
title_short Identification and functional analysis of beta-tubulin genes by site specific integrative transformation in Aspergillus nidulans
title_sort identification and functional analysis of beta-tubulin genes by site specific integrative transformation in aspergillus nidulans
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2113715/
https://www.ncbi.nlm.nih.gov/pubmed/3897247