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Characterization of human Ccser2 as a protein tracking the plus-ends of microtubules

OBJECTIVE: Microtubules, which are closely related to cell proliferation, have been the promising therapeutic target of cancer. Therefore, it is necessary to understand the intracellular control mechanisms of microtubules, the whole picture of which is still unclear though. Intracellular dynamics of...

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Autores principales: Shirai, Yuko, Okuda, Tomohiro, Oshima, Kenzi, Nadano, Daita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10486078/
https://www.ncbi.nlm.nih.gov/pubmed/37684684
http://dx.doi.org/10.1186/s13104-023-06475-z
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author Shirai, Yuko
Okuda, Tomohiro
Oshima, Kenzi
Nadano, Daita
author_facet Shirai, Yuko
Okuda, Tomohiro
Oshima, Kenzi
Nadano, Daita
author_sort Shirai, Yuko
collection PubMed
description OBJECTIVE: Microtubules, which are closely related to cell proliferation, have been the promising therapeutic target of cancer. Therefore, it is necessary to understand the intracellular control mechanisms of microtubules, the whole picture of which is still unclear though. Intracellular dynamics of microtubules are regulated by various microtubule-associated proteins, one group of which is microtubule plus-end-tracking proteins (+ TIPs), localizing to the extending tips of microtubules. Here, we report the identification and analysis of Ccser2 as a new + TIP in human breast cancer MCF-7 cells. RESULTS: Ccser2 was found to be a member of + TIPs by microscopic observations including time-lapse imaging. The C-terminal region of Ccser2, including two SxIP motifs, was likely to be important for the tracking function. In MCF-7 cells, endogenous Ccser2 was mainly detected in the peripheral regions of microtubule fibers, suggesting that Ccser2 functions in cell projections. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13104-023-06475-z.
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spelling pubmed-104860782023-09-09 Characterization of human Ccser2 as a protein tracking the plus-ends of microtubules Shirai, Yuko Okuda, Tomohiro Oshima, Kenzi Nadano, Daita BMC Res Notes Research Note OBJECTIVE: Microtubules, which are closely related to cell proliferation, have been the promising therapeutic target of cancer. Therefore, it is necessary to understand the intracellular control mechanisms of microtubules, the whole picture of which is still unclear though. Intracellular dynamics of microtubules are regulated by various microtubule-associated proteins, one group of which is microtubule plus-end-tracking proteins (+ TIPs), localizing to the extending tips of microtubules. Here, we report the identification and analysis of Ccser2 as a new + TIP in human breast cancer MCF-7 cells. RESULTS: Ccser2 was found to be a member of + TIPs by microscopic observations including time-lapse imaging. The C-terminal region of Ccser2, including two SxIP motifs, was likely to be important for the tracking function. In MCF-7 cells, endogenous Ccser2 was mainly detected in the peripheral regions of microtubule fibers, suggesting that Ccser2 functions in cell projections. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13104-023-06475-z. BioMed Central 2023-09-08 /pmc/articles/PMC10486078/ /pubmed/37684684 http://dx.doi.org/10.1186/s13104-023-06475-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Note
Shirai, Yuko
Okuda, Tomohiro
Oshima, Kenzi
Nadano, Daita
Characterization of human Ccser2 as a protein tracking the plus-ends of microtubules
title Characterization of human Ccser2 as a protein tracking the plus-ends of microtubules
title_full Characterization of human Ccser2 as a protein tracking the plus-ends of microtubules
title_fullStr Characterization of human Ccser2 as a protein tracking the plus-ends of microtubules
title_full_unstemmed Characterization of human Ccser2 as a protein tracking the plus-ends of microtubules
title_short Characterization of human Ccser2 as a protein tracking the plus-ends of microtubules
title_sort characterization of human ccser2 as a protein tracking the plus-ends of microtubules
topic Research Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10486078/
https://www.ncbi.nlm.nih.gov/pubmed/37684684
http://dx.doi.org/10.1186/s13104-023-06475-z
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