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Cytoplasmic Transport Machinery of the SPF27 Homologue Num1 in Ustilago maydis

In the phytopathogenic basidiomycete Ustilago maydis, the Num1 protein has a pivotal function in hyphal morphogenesis. Num1 functions as a core component of the spliceosome-associated Prp19/CDC5 complex (NTC). The interaction of Num1 with the kinesin motor Kin1 suggests a connection between a compon...

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Autores principales: Zhou, Lu, Obhof, Theresa, Schneider, Karina, Feldbrügge, Michael, Nienhaus, G. Ulrich, Kämper, Jörg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832149/
https://www.ncbi.nlm.nih.gov/pubmed/29483520
http://dx.doi.org/10.1038/s41598-018-21628-y
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author Zhou, Lu
Obhof, Theresa
Schneider, Karina
Feldbrügge, Michael
Nienhaus, G. Ulrich
Kämper, Jörg
author_facet Zhou, Lu
Obhof, Theresa
Schneider, Karina
Feldbrügge, Michael
Nienhaus, G. Ulrich
Kämper, Jörg
author_sort Zhou, Lu
collection PubMed
description In the phytopathogenic basidiomycete Ustilago maydis, the Num1 protein has a pivotal function in hyphal morphogenesis. Num1 functions as a core component of the spliceosome-associated Prp19/CDC5 complex (NTC). The interaction of Num1 with the kinesin motor Kin1 suggests a connection between a component of the splicing machinery and cytoplasmic trafficking processes. Previously it was shown that Num1 localizes predominantly in the nucleus; however, due to the diffraction-limited spatial resolution of conventional optical microscopy, it was not possible to attribute the localization to specific structures within the cytoplasm. We have now employed super-resolution localization microscopy to visualize Num1 in the cytoplasm by fusing it to a tandem dimeric Eos fluorescent protein (tdEosFP). The Num1 protein is localized within the cytoplasm with an enhanced density in the vicinity of microtubules. Num1 movement is found predominantly close to the nucleus. Movement is dependent on its interaction partner Kin1, but independent of Kin3. Our results provide strong evidence that, in addition to its involvement in splicing in the nucleus, Num1 has an additional functional role in the cytosol connected to the Kin1 motor protein.
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spelling pubmed-58321492018-03-05 Cytoplasmic Transport Machinery of the SPF27 Homologue Num1 in Ustilago maydis Zhou, Lu Obhof, Theresa Schneider, Karina Feldbrügge, Michael Nienhaus, G. Ulrich Kämper, Jörg Sci Rep Article In the phytopathogenic basidiomycete Ustilago maydis, the Num1 protein has a pivotal function in hyphal morphogenesis. Num1 functions as a core component of the spliceosome-associated Prp19/CDC5 complex (NTC). The interaction of Num1 with the kinesin motor Kin1 suggests a connection between a component of the splicing machinery and cytoplasmic trafficking processes. Previously it was shown that Num1 localizes predominantly in the nucleus; however, due to the diffraction-limited spatial resolution of conventional optical microscopy, it was not possible to attribute the localization to specific structures within the cytoplasm. We have now employed super-resolution localization microscopy to visualize Num1 in the cytoplasm by fusing it to a tandem dimeric Eos fluorescent protein (tdEosFP). The Num1 protein is localized within the cytoplasm with an enhanced density in the vicinity of microtubules. Num1 movement is found predominantly close to the nucleus. Movement is dependent on its interaction partner Kin1, but independent of Kin3. Our results provide strong evidence that, in addition to its involvement in splicing in the nucleus, Num1 has an additional functional role in the cytosol connected to the Kin1 motor protein. Nature Publishing Group UK 2018-02-26 /pmc/articles/PMC5832149/ /pubmed/29483520 http://dx.doi.org/10.1038/s41598-018-21628-y Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Zhou, Lu
Obhof, Theresa
Schneider, Karina
Feldbrügge, Michael
Nienhaus, G. Ulrich
Kämper, Jörg
Cytoplasmic Transport Machinery of the SPF27 Homologue Num1 in Ustilago maydis
title Cytoplasmic Transport Machinery of the SPF27 Homologue Num1 in Ustilago maydis
title_full Cytoplasmic Transport Machinery of the SPF27 Homologue Num1 in Ustilago maydis
title_fullStr Cytoplasmic Transport Machinery of the SPF27 Homologue Num1 in Ustilago maydis
title_full_unstemmed Cytoplasmic Transport Machinery of the SPF27 Homologue Num1 in Ustilago maydis
title_short Cytoplasmic Transport Machinery of the SPF27 Homologue Num1 in Ustilago maydis
title_sort cytoplasmic transport machinery of the spf27 homologue num1 in ustilago maydis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832149/
https://www.ncbi.nlm.nih.gov/pubmed/29483520
http://dx.doi.org/10.1038/s41598-018-21628-y
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