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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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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. |
format | Online Article Text |
id | pubmed-5832149 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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