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Elk1 affects katanin and spastin proteins via differential transcriptional and post-transcriptional regulations

Microtubule severing, which is highly critical for the survival of both mitotic and post-mitotic cells, has to be precisely adjusted by regulating the expression levels of severing proteins, katanin and spastin. Even though severing mechanism is relatively well-studied, there are limited studies for...

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Autores principales: Kelle, Dolunay, Kırımtay, Koray, Selçuk, Ece, Karabay, Arzu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6383945/
https://www.ncbi.nlm.nih.gov/pubmed/30789974
http://dx.doi.org/10.1371/journal.pone.0212518
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author Kelle, Dolunay
Kırımtay, Koray
Selçuk, Ece
Karabay, Arzu
author_facet Kelle, Dolunay
Kırımtay, Koray
Selçuk, Ece
Karabay, Arzu
author_sort Kelle, Dolunay
collection PubMed
description Microtubule severing, which is highly critical for the survival of both mitotic and post-mitotic cells, has to be precisely adjusted by regulating the expression levels of severing proteins, katanin and spastin. Even though severing mechanism is relatively well-studied, there are limited studies for the transcriptional regulation of microtubule severing proteins. In this study, we identified the main regulatory region of KATNA1 gene encoding katanin-p60 as 5’ UTR, which has a key role for its expression, and showed Elk1 binding to KATNA1. Furthermore, we identified that Elk1 decreased katanin-p60 and spastin protein expressions, while mRNA levels were increased upon Elk1 overexpression. In addition, SUMOylation is a known post-translational modification regulating Elk1 activity. A previous study suggested that K230, K249, K254 amino acids in the R domain are the main SUMOylation sites; however, we identified that these amino acids are neither essential nor substantial for Elk1 SUMOylation. Also, we determined that KATNA1 methylation results in the reduction of Elk1 binding whereas SPG4 methylation does not. Together, our findings emphasizing the impacts of both transcriptional and post-transcriptional regulations of katanin-p60 and spastin suggest that Elk1 has a key role for differential expression patterns of microtubule severing proteins, thereby regulating cellular functions through alterations of microtubule organization.
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spelling pubmed-63839452019-03-09 Elk1 affects katanin and spastin proteins via differential transcriptional and post-transcriptional regulations Kelle, Dolunay Kırımtay, Koray Selçuk, Ece Karabay, Arzu PLoS One Research Article Microtubule severing, which is highly critical for the survival of both mitotic and post-mitotic cells, has to be precisely adjusted by regulating the expression levels of severing proteins, katanin and spastin. Even though severing mechanism is relatively well-studied, there are limited studies for the transcriptional regulation of microtubule severing proteins. In this study, we identified the main regulatory region of KATNA1 gene encoding katanin-p60 as 5’ UTR, which has a key role for its expression, and showed Elk1 binding to KATNA1. Furthermore, we identified that Elk1 decreased katanin-p60 and spastin protein expressions, while mRNA levels were increased upon Elk1 overexpression. In addition, SUMOylation is a known post-translational modification regulating Elk1 activity. A previous study suggested that K230, K249, K254 amino acids in the R domain are the main SUMOylation sites; however, we identified that these amino acids are neither essential nor substantial for Elk1 SUMOylation. Also, we determined that KATNA1 methylation results in the reduction of Elk1 binding whereas SPG4 methylation does not. Together, our findings emphasizing the impacts of both transcriptional and post-transcriptional regulations of katanin-p60 and spastin suggest that Elk1 has a key role for differential expression patterns of microtubule severing proteins, thereby regulating cellular functions through alterations of microtubule organization. Public Library of Science 2019-02-21 /pmc/articles/PMC6383945/ /pubmed/30789974 http://dx.doi.org/10.1371/journal.pone.0212518 Text en © 2019 Kelle et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kelle, Dolunay
Kırımtay, Koray
Selçuk, Ece
Karabay, Arzu
Elk1 affects katanin and spastin proteins via differential transcriptional and post-transcriptional regulations
title Elk1 affects katanin and spastin proteins via differential transcriptional and post-transcriptional regulations
title_full Elk1 affects katanin and spastin proteins via differential transcriptional and post-transcriptional regulations
title_fullStr Elk1 affects katanin and spastin proteins via differential transcriptional and post-transcriptional regulations
title_full_unstemmed Elk1 affects katanin and spastin proteins via differential transcriptional and post-transcriptional regulations
title_short Elk1 affects katanin and spastin proteins via differential transcriptional and post-transcriptional regulations
title_sort elk1 affects katanin and spastin proteins via differential transcriptional and post-transcriptional regulations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6383945/
https://www.ncbi.nlm.nih.gov/pubmed/30789974
http://dx.doi.org/10.1371/journal.pone.0212518
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