Cochicine-induced polyploidization depends on tubulin polymerization in c-metaphase cells

Bibliographic Details
Main Author: Caperta, A.
Publication Date: 2006
Other Authors: Delgado, M., Ressurreição, F., Meister, A., Jones, R.N., Viegas, W., Houben, A.
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10400.5/2845
Summary: The microtubule cytoskeleton plays a crucial role in the cell cycle and in mitosis. Colchicine is a microtubule-depolymerizing agent that has long been used to induce chromosome individualization in cells arrested at metaphase and also in the induction of polyploid plants. Although attempts have been made to explain the processes and mechanisms underlying polyploidy induction, the role of the cytoskeleton still remains largely unknown. Through immunodetection of alpha-tubulin, different concentrations (0.5 or 5 mM) of colchicine were found to produce opposite effects in the organization of the cytoskeleton in rye (Secale cereale L.). A low concentration (0.5 mM) induced depolymerization of the microtubular cytoskeleton in all phases of the cell cycle. In contrast, a high concentration (5 mM) was found to induce the polymerization of new tubulin-containing structures in c-metaphase cells. Furthermore, both treatments also showed contrasting effects in the induction of polyploid cells. Flow cytometric analysis and quantitative assessments of nucleolus-organizing regions revealed that only the high-concentration colchicine treatment was effective in the formation of polyploid cells. Our studies indicate that spindle disruption alone is insufficient for the induction of polyploid cells. The absence of any tubulin structures in plants treated with colchicine at the low concentration induced cell anomalies, such as the occurrence of nuclei with irregular shape and/or (additional) micronuclei, 12 h after recovery, pointing to a direct effect on cell viability. In contrast, the almost insignificant level of cell anomalies in the high-concentration treatment suggests that the presence of new tubulin- containing structures allows the reconstitution of 4C nuclei and their progression into the cell cycle.
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spelling Cochicine-induced polyploidization depends on tubulin polymerization in c-metaphase cellsinduced polyploidycolchicinetubulin arraySecale cerealeThe microtubule cytoskeleton plays a crucial role in the cell cycle and in mitosis. Colchicine is a microtubule-depolymerizing agent that has long been used to induce chromosome individualization in cells arrested at metaphase and also in the induction of polyploid plants. Although attempts have been made to explain the processes and mechanisms underlying polyploidy induction, the role of the cytoskeleton still remains largely unknown. Through immunodetection of alpha-tubulin, different concentrations (0.5 or 5 mM) of colchicine were found to produce opposite effects in the organization of the cytoskeleton in rye (Secale cereale L.). A low concentration (0.5 mM) induced depolymerization of the microtubular cytoskeleton in all phases of the cell cycle. In contrast, a high concentration (5 mM) was found to induce the polymerization of new tubulin-containing structures in c-metaphase cells. Furthermore, both treatments also showed contrasting effects in the induction of polyploid cells. Flow cytometric analysis and quantitative assessments of nucleolus-organizing regions revealed that only the high-concentration colchicine treatment was effective in the formation of polyploid cells. Our studies indicate that spindle disruption alone is insufficient for the induction of polyploid cells. The absence of any tubulin structures in plants treated with colchicine at the low concentration induced cell anomalies, such as the occurrence of nuclei with irregular shape and/or (additional) micronuclei, 12 h after recovery, pointing to a direct effect on cell viability. In contrast, the almost insignificant level of cell anomalies in the high-concentration treatment suggests that the presence of new tubulin- containing structures allows the reconstitution of 4C nuclei and their progression into the cell cycle.SpringerRepositório da Universidade de LisboaCaperta, A.Delgado, M.Ressurreição, F.Meister, A.Jones, R.N.Viegas, W.Houben, A.2011-01-24T14:53:08Z20062006-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.5/2845eng"Protoplasma". 227 (2006) 147-153DOI 10.1007/s00709-005-0137-zinfo: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:RCAAP2025-03-17T16:00:11Zoai:repositorio.ulisboa.pt:10400.5/2845Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T03:59:53.367720Repositórios 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 Cochicine-induced polyploidization depends on tubulin polymerization in c-metaphase cells
title Cochicine-induced polyploidization depends on tubulin polymerization in c-metaphase cells
spellingShingle Cochicine-induced polyploidization depends on tubulin polymerization in c-metaphase cells
Caperta, A.
induced polyploidy
colchicine
tubulin array
Secale cereale
title_short Cochicine-induced polyploidization depends on tubulin polymerization in c-metaphase cells
title_full Cochicine-induced polyploidization depends on tubulin polymerization in c-metaphase cells
title_fullStr Cochicine-induced polyploidization depends on tubulin polymerization in c-metaphase cells
title_full_unstemmed Cochicine-induced polyploidization depends on tubulin polymerization in c-metaphase cells
title_sort Cochicine-induced polyploidization depends on tubulin polymerization in c-metaphase cells
author Caperta, A.
author_facet Caperta, A.
Delgado, M.
Ressurreição, F.
Meister, A.
Jones, R.N.
Viegas, W.
Houben, A.
author_role author
author2 Delgado, M.
Ressurreição, F.
Meister, A.
Jones, R.N.
Viegas, W.
Houben, A.
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório da Universidade de Lisboa
dc.contributor.author.fl_str_mv Caperta, A.
Delgado, M.
Ressurreição, F.
Meister, A.
Jones, R.N.
Viegas, W.
Houben, A.
dc.subject.por.fl_str_mv induced polyploidy
colchicine
tubulin array
Secale cereale
topic induced polyploidy
colchicine
tubulin array
Secale cereale
description The microtubule cytoskeleton plays a crucial role in the cell cycle and in mitosis. Colchicine is a microtubule-depolymerizing agent that has long been used to induce chromosome individualization in cells arrested at metaphase and also in the induction of polyploid plants. Although attempts have been made to explain the processes and mechanisms underlying polyploidy induction, the role of the cytoskeleton still remains largely unknown. Through immunodetection of alpha-tubulin, different concentrations (0.5 or 5 mM) of colchicine were found to produce opposite effects in the organization of the cytoskeleton in rye (Secale cereale L.). A low concentration (0.5 mM) induced depolymerization of the microtubular cytoskeleton in all phases of the cell cycle. In contrast, a high concentration (5 mM) was found to induce the polymerization of new tubulin-containing structures in c-metaphase cells. Furthermore, both treatments also showed contrasting effects in the induction of polyploid cells. Flow cytometric analysis and quantitative assessments of nucleolus-organizing regions revealed that only the high-concentration colchicine treatment was effective in the formation of polyploid cells. Our studies indicate that spindle disruption alone is insufficient for the induction of polyploid cells. The absence of any tubulin structures in plants treated with colchicine at the low concentration induced cell anomalies, such as the occurrence of nuclei with irregular shape and/or (additional) micronuclei, 12 h after recovery, pointing to a direct effect on cell viability. In contrast, the almost insignificant level of cell anomalies in the high-concentration treatment suggests that the presence of new tubulin- containing structures allows the reconstitution of 4C nuclei and their progression into the cell cycle.
publishDate 2006
dc.date.none.fl_str_mv 2006
2006-01-01T00:00:00Z
2011-01-24T14:53:08Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.5/2845
url http://hdl.handle.net/10400.5/2845
dc.language.iso.fl_str_mv eng
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dc.relation.none.fl_str_mv "Protoplasma". 227 (2006) 147-153
DOI 10.1007/s00709-005-0137-z
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Springer
publisher.none.fl_str_mv Springer
dc.source.none.fl_str_mv reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
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