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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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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. |
format | Online Article Text |
id | pubmed-10486078 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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