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The posttranslational modification of tubulin undergoes a switch from detyrosination to acetylation as epithelial cells become polarized
Tubulin posttranslational modifications (PTMs) have been suggested to provide navigational cues for molecular motors to deliver cargo to spatially segregated subcellular domains, but the molecular details of this process remain unclear. Here we show that in Madin-Darby Canine Kidney (MDCK) epithelia...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069008/ https://www.ncbi.nlm.nih.gov/pubmed/21307336 http://dx.doi.org/10.1091/mbc.E10-06-0519 |
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author | Quinones, Geraldine B. Danowski, Barbara A. Devaraj, Anjan Singh, Vimla Ligon, Lee A. |
author_facet | Quinones, Geraldine B. Danowski, Barbara A. Devaraj, Anjan Singh, Vimla Ligon, Lee A. |
author_sort | Quinones, Geraldine B. |
collection | PubMed |
description | Tubulin posttranslational modifications (PTMs) have been suggested to provide navigational cues for molecular motors to deliver cargo to spatially segregated subcellular domains, but the molecular details of this process remain unclear. Here we show that in Madin-Darby Canine Kidney (MDCK) epithelial cells, microtubules express several tubulin PTMs. These modifications, however, are not coordinated, and cells have multiple subpopulations of microtubules that are marked by different combinations of PTMs. Furthermore these subpopulations show differential sensitivity to both drug- and cold-induced depolymerization, suggesting that they are functionally different as well. The composition and distribution of modified microtubules change as cells undergo the morphogenesis associated with polarization. Two-dimensionally polarized spreading cells have more detyrosinated microtubules that are oriented toward the leading edge, but three-dimensionally polarized cells have more acetylated microtubules that are oriented toward the apical domain. These data suggest that the transition from 2D polarity to 3D polarity involves both a reorganization of the microtubule cytoskeleton and a change in tubulin PTMs. However, in both 2D polarized and 3D polarized cells, the modified microtubules are oriented to support vectorial cargo transport to areas of high need. |
format | Text |
id | pubmed-3069008 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-30690082011-06-16 The posttranslational modification of tubulin undergoes a switch from detyrosination to acetylation as epithelial cells become polarized Quinones, Geraldine B. Danowski, Barbara A. Devaraj, Anjan Singh, Vimla Ligon, Lee A. Mol Biol Cell Articles Tubulin posttranslational modifications (PTMs) have been suggested to provide navigational cues for molecular motors to deliver cargo to spatially segregated subcellular domains, but the molecular details of this process remain unclear. Here we show that in Madin-Darby Canine Kidney (MDCK) epithelial cells, microtubules express several tubulin PTMs. These modifications, however, are not coordinated, and cells have multiple subpopulations of microtubules that are marked by different combinations of PTMs. Furthermore these subpopulations show differential sensitivity to both drug- and cold-induced depolymerization, suggesting that they are functionally different as well. The composition and distribution of modified microtubules change as cells undergo the morphogenesis associated with polarization. Two-dimensionally polarized spreading cells have more detyrosinated microtubules that are oriented toward the leading edge, but three-dimensionally polarized cells have more acetylated microtubules that are oriented toward the apical domain. These data suggest that the transition from 2D polarity to 3D polarity involves both a reorganization of the microtubule cytoskeleton and a change in tubulin PTMs. However, in both 2D polarized and 3D polarized cells, the modified microtubules are oriented to support vectorial cargo transport to areas of high need. The American Society for Cell Biology 2011-04-01 /pmc/articles/PMC3069008/ /pubmed/21307336 http://dx.doi.org/10.1091/mbc.E10-06-0519 Text en © 2011 Quinones et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,“ “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society of Cell Biology. |
spellingShingle | Articles Quinones, Geraldine B. Danowski, Barbara A. Devaraj, Anjan Singh, Vimla Ligon, Lee A. The posttranslational modification of tubulin undergoes a switch from detyrosination to acetylation as epithelial cells become polarized |
title | The posttranslational modification of tubulin undergoes a switch from detyrosination to acetylation as epithelial cells become polarized |
title_full | The posttranslational modification of tubulin undergoes a switch from detyrosination to acetylation as epithelial cells become polarized |
title_fullStr | The posttranslational modification of tubulin undergoes a switch from detyrosination to acetylation as epithelial cells become polarized |
title_full_unstemmed | The posttranslational modification of tubulin undergoes a switch from detyrosination to acetylation as epithelial cells become polarized |
title_short | The posttranslational modification of tubulin undergoes a switch from detyrosination to acetylation as epithelial cells become polarized |
title_sort | posttranslational modification of tubulin undergoes a switch from detyrosination to acetylation as epithelial cells become polarized |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069008/ https://www.ncbi.nlm.nih.gov/pubmed/21307336 http://dx.doi.org/10.1091/mbc.E10-06-0519 |
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