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Xenopus TACC1 is a microtubule plus‐end tracking protein that can regulate microtubule dynamics during embryonic development

Microtubule plus‐end dynamics are regulated by a family of proteins called plus‐end tracking proteins (+TIPs). We recently demonstrated that the transforming acidic coiled‐coil (TACC) domain family member, TACC3, can function as a +TIP to regulate microtubule dynamics in Xenopus laevis embryonic cel...

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Autores principales: Lucaj, Christopher M., Evans, Matthew F., Nwagbara, Belinda U., Ebbert, Patrick T., Baker, Charlie C., Volk, Joseph G., Francl, Andrew F., Ruvolo, Sean P., Lowery, Laura Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4520305/
https://www.ncbi.nlm.nih.gov/pubmed/26012630
http://dx.doi.org/10.1002/cm.21224
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author Lucaj, Christopher M.
Evans, Matthew F.
Nwagbara, Belinda U.
Ebbert, Patrick T.
Baker, Charlie C.
Volk, Joseph G.
Francl, Andrew F.
Ruvolo, Sean P.
Lowery, Laura Anne
author_facet Lucaj, Christopher M.
Evans, Matthew F.
Nwagbara, Belinda U.
Ebbert, Patrick T.
Baker, Charlie C.
Volk, Joseph G.
Francl, Andrew F.
Ruvolo, Sean P.
Lowery, Laura Anne
author_sort Lucaj, Christopher M.
collection PubMed
description Microtubule plus‐end dynamics are regulated by a family of proteins called plus‐end tracking proteins (+TIPs). We recently demonstrated that the transforming acidic coiled‐coil (TACC) domain family member, TACC3, can function as a +TIP to regulate microtubule dynamics in Xenopus laevis embryonic cells. Although it has been previously reported that TACC3 is the only TACC family member that exists in Xenopus, our examination of its genome determined that Xenopus, like all other vertebrates, contains three TACC family members. Here, we investigate the localization and function of Xenopus TACC1, the founding member of the TACC family. We demonstrate that it can act as a +TIP to regulate microtubule dynamics, and that the conserved C‐terminal TACC domain is required for its localization to plus‐ends. We also show that, in Xenopus embryonic mesenchymal cells, TACC1 and TACC3 are each required for maintaining normal microtubule growth speed but exhibit some functional redundancy in the regulation of microtubule growth lifetime. Given the conservation of TACC1 in Xenopus and other vertebrates, we propose that Xenopus laevis is a useful system to investigate unexplored cell biological functions of TACC1 and other TACC family members in the regulation of microtubule dynamics. © 2015 The Authors. Cytoskeleton, Published by Wiley Periodicals, Inc.
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spelling pubmed-45203052015-07-30 Xenopus TACC1 is a microtubule plus‐end tracking protein that can regulate microtubule dynamics during embryonic development Lucaj, Christopher M. Evans, Matthew F. Nwagbara, Belinda U. Ebbert, Patrick T. Baker, Charlie C. Volk, Joseph G. Francl, Andrew F. Ruvolo, Sean P. Lowery, Laura Anne Cytoskeleton (Hoboken) Short Report Microtubule plus‐end dynamics are regulated by a family of proteins called plus‐end tracking proteins (+TIPs). We recently demonstrated that the transforming acidic coiled‐coil (TACC) domain family member, TACC3, can function as a +TIP to regulate microtubule dynamics in Xenopus laevis embryonic cells. Although it has been previously reported that TACC3 is the only TACC family member that exists in Xenopus, our examination of its genome determined that Xenopus, like all other vertebrates, contains three TACC family members. Here, we investigate the localization and function of Xenopus TACC1, the founding member of the TACC family. We demonstrate that it can act as a +TIP to regulate microtubule dynamics, and that the conserved C‐terminal TACC domain is required for its localization to plus‐ends. We also show that, in Xenopus embryonic mesenchymal cells, TACC1 and TACC3 are each required for maintaining normal microtubule growth speed but exhibit some functional redundancy in the regulation of microtubule growth lifetime. Given the conservation of TACC1 in Xenopus and other vertebrates, we propose that Xenopus laevis is a useful system to investigate unexplored cell biological functions of TACC1 and other TACC family members in the regulation of microtubule dynamics. © 2015 The Authors. Cytoskeleton, Published by Wiley Periodicals, Inc. John Wiley and Sons Inc. 2015-07-14 2015-05 /pmc/articles/PMC4520305/ /pubmed/26012630 http://dx.doi.org/10.1002/cm.21224 Text en © 2015 The Authors. Cytoskeleton, Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Short Report
Lucaj, Christopher M.
Evans, Matthew F.
Nwagbara, Belinda U.
Ebbert, Patrick T.
Baker, Charlie C.
Volk, Joseph G.
Francl, Andrew F.
Ruvolo, Sean P.
Lowery, Laura Anne
Xenopus TACC1 is a microtubule plus‐end tracking protein that can regulate microtubule dynamics during embryonic development
title Xenopus TACC1 is a microtubule plus‐end tracking protein that can regulate microtubule dynamics during embryonic development
title_full Xenopus TACC1 is a microtubule plus‐end tracking protein that can regulate microtubule dynamics during embryonic development
title_fullStr Xenopus TACC1 is a microtubule plus‐end tracking protein that can regulate microtubule dynamics during embryonic development
title_full_unstemmed Xenopus TACC1 is a microtubule plus‐end tracking protein that can regulate microtubule dynamics during embryonic development
title_short Xenopus TACC1 is a microtubule plus‐end tracking protein that can regulate microtubule dynamics during embryonic development
title_sort xenopus tacc1 is a microtubule plus‐end tracking protein that can regulate microtubule dynamics during embryonic development
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4520305/
https://www.ncbi.nlm.nih.gov/pubmed/26012630
http://dx.doi.org/10.1002/cm.21224
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