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Tubulin post-translational modifications: the elusive roles of acetylation

Bibliographic Details
Main Author: Carmona, Bruno
Publication Date: 2023
Other Authors: Marinho, H. Susana, Matos, Catarina Lopes, Nolasco, S., Soares, Helena
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10400.21/15919
Summary: Microtubules (MTs), dynamic polymers of α/β-tubulin heterodimers found in all eukaryotes, are involved in cytoplasm spatial organization, intracellular transport, cell polarity, migration, division, and cilia biology. MTs functional diversity depends on the differential expression of distinct tubulin isotypes and is amplified by a vast number of different post-translational modifications (PTMs). The addition/removal of PTMs to α- or β-tubulins is catalyzed by specific enzymes and allows combinatory patterns largely enriching the distinct biochemical and biophysical properties of MTs, creating a code read by distinct proteins, including microtubule-associated proteins (MAPs), which allow cellular responses. This review is focused on tubulin-acetylation, whose cellular roles continue to generate debate. We travel through the experimental data pointing to α-tubulin Lys40 acetylation role as being an MT stabilizer and a typical PTM of long-lived MTs, to the most recent data, suggesting that Lys40 acetylation enhances MT flexibility and alters the mechanical properties of MTs, preventing MTs from mechanical aging characterized by structural damage. Additionally, we discuss the regulation of tubulin acetyltransferases/desacetylases and their impacts on cell physiology. Finally, we analyze how changes in MT acetylation levels have been found to be a general response to stress and how they are associated with several human pathologies.
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spelling Tubulin post-translational modifications: the elusive roles of acetylationAcetylationTubulinLys40MicrotubulesPost-translational modificationsαTAT1HDAC6SIRT2Microtubule-associated proteinsMicrotubule-mechanical propertiesIPL/2021/ObeCil_ESTeSLIPL/2022/WintCilGlu_ESTeSLMicrotubules (MTs), dynamic polymers of α/β-tubulin heterodimers found in all eukaryotes, are involved in cytoplasm spatial organization, intracellular transport, cell polarity, migration, division, and cilia biology. MTs functional diversity depends on the differential expression of distinct tubulin isotypes and is amplified by a vast number of different post-translational modifications (PTMs). The addition/removal of PTMs to α- or β-tubulins is catalyzed by specific enzymes and allows combinatory patterns largely enriching the distinct biochemical and biophysical properties of MTs, creating a code read by distinct proteins, including microtubule-associated proteins (MAPs), which allow cellular responses. This review is focused on tubulin-acetylation, whose cellular roles continue to generate debate. We travel through the experimental data pointing to α-tubulin Lys40 acetylation role as being an MT stabilizer and a typical PTM of long-lived MTs, to the most recent data, suggesting that Lys40 acetylation enhances MT flexibility and alters the mechanical properties of MTs, preventing MTs from mechanical aging characterized by structural damage. Additionally, we discuss the regulation of tubulin acetyltransferases/desacetylases and their impacts on cell physiology. Finally, we analyze how changes in MT acetylation levels have been found to be a general response to stress and how they are associated with several human pathologies.RCIPLCarmona, BrunoMarinho, H. SusanaMatos, Catarina LopesNolasco, S.Soares, Helena2023-04-20T15:23:15Z2023-042023-04-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.21/15919eng10.3390/biology12040561info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-02-12T09:36:19Zoai:repositorio.ipl.pt:10400.21/15919Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T20:02:02.327400Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Tubulin post-translational modifications: the elusive roles of acetylation
title Tubulin post-translational modifications: the elusive roles of acetylation
spellingShingle Tubulin post-translational modifications: the elusive roles of acetylation
Carmona, Bruno
Acetylation
Tubulin
Lys40
Microtubules
Post-translational modifications
αTAT1
HDAC6
SIRT2
Microtubule-associated proteins
Microtubule-mechanical properties
IPL/2021/ObeCil_ESTeSL
IPL/2022/WintCilGlu_ESTeSL
title_short Tubulin post-translational modifications: the elusive roles of acetylation
title_full Tubulin post-translational modifications: the elusive roles of acetylation
title_fullStr Tubulin post-translational modifications: the elusive roles of acetylation
title_full_unstemmed Tubulin post-translational modifications: the elusive roles of acetylation
title_sort Tubulin post-translational modifications: the elusive roles of acetylation
author Carmona, Bruno
author_facet Carmona, Bruno
Marinho, H. Susana
Matos, Catarina Lopes
Nolasco, S.
Soares, Helena
author_role author
author2 Marinho, H. Susana
Matos, Catarina Lopes
Nolasco, S.
Soares, Helena
author2_role author
author
author
author
dc.contributor.none.fl_str_mv RCIPL
dc.contributor.author.fl_str_mv Carmona, Bruno
Marinho, H. Susana
Matos, Catarina Lopes
Nolasco, S.
Soares, Helena
dc.subject.por.fl_str_mv Acetylation
Tubulin
Lys40
Microtubules
Post-translational modifications
αTAT1
HDAC6
SIRT2
Microtubule-associated proteins
Microtubule-mechanical properties
IPL/2021/ObeCil_ESTeSL
IPL/2022/WintCilGlu_ESTeSL
topic Acetylation
Tubulin
Lys40
Microtubules
Post-translational modifications
αTAT1
HDAC6
SIRT2
Microtubule-associated proteins
Microtubule-mechanical properties
IPL/2021/ObeCil_ESTeSL
IPL/2022/WintCilGlu_ESTeSL
description Microtubules (MTs), dynamic polymers of α/β-tubulin heterodimers found in all eukaryotes, are involved in cytoplasm spatial organization, intracellular transport, cell polarity, migration, division, and cilia biology. MTs functional diversity depends on the differential expression of distinct tubulin isotypes and is amplified by a vast number of different post-translational modifications (PTMs). The addition/removal of PTMs to α- or β-tubulins is catalyzed by specific enzymes and allows combinatory patterns largely enriching the distinct biochemical and biophysical properties of MTs, creating a code read by distinct proteins, including microtubule-associated proteins (MAPs), which allow cellular responses. This review is focused on tubulin-acetylation, whose cellular roles continue to generate debate. We travel through the experimental data pointing to α-tubulin Lys40 acetylation role as being an MT stabilizer and a typical PTM of long-lived MTs, to the most recent data, suggesting that Lys40 acetylation enhances MT flexibility and alters the mechanical properties of MTs, preventing MTs from mechanical aging characterized by structural damage. Additionally, we discuss the regulation of tubulin acetyltransferases/desacetylases and their impacts on cell physiology. Finally, we analyze how changes in MT acetylation levels have been found to be a general response to stress and how they are associated with several human pathologies.
publishDate 2023
dc.date.none.fl_str_mv 2023-04-20T15:23:15Z
2023-04
2023-04-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.21/15919
url http://hdl.handle.net/10400.21/15919
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.3390/biology12040561
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dc.source.none.fl_str_mv reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
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instname_str FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
instacron_str RCAAP
institution RCAAP
reponame_str Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
collection Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
repository.name.fl_str_mv Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
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