Utilize este identificador para referenciar este registo: http://hdl.handle.net/10400.21/3046
Título: Subunits of the chaperonin CCT are associated with Tetrahymena microtubule structures and are involved in cilia biogenesis
Autor: Seixas, Cecília
Casalou, Cristina
Melo, Luís Viseu
Nolasco, Sofia
Brogueira, Pedro
Soares, Helena
Palavras-chave: Chaperonin-CCT
Blotting, Western
Chaperonin containing TCP-1
Fluorescent antibody technique
Protein folding
Protein transport
Protozoan proteins
Data: Nov-2003
Editora: Elsevier
Citação: Seixas C, Casalou C, Melo LV, Nolasco S, Brogueira P, Soares H. Subunits of the chaperonin CCT are associated with Tetrahymena microtubule structures and are involved in cilia biogenesis. Exp Cell Res. 2003;290(2):303-21.
Resumo: The cytosolic chaperonin CCT is a heterooligomeric complex of about 900 kDa that mediates the folding of cytoskeletal proteins. We observed by indirect immunofluorescence that the Tetrahymena TpCCTalpha, TpCCTdelta, TpCCTepsilon, and TpCCTeta-subunits colocalize with tubulin in cilia, basal bodies, oral apparatus, and contractile vacuole pores. TpCCT-subunits localization was affected during reciliation. These findings combined with atomic force microscopy measurements in reciliating cells indicate that these proteins play a role during cilia biogenesis related to microtubule nucleation, tubulin transport, and/or axoneme assembly. The TpCCT-subunits were also found to be associated with cortex and cytoplasmic microtubules suggesting that they can act as microtubule-associated proteins. The TpCCTdelta being the only subunit found associated with the macronuclear envelope indicates that it has functions outside of the 900 kDa complex. Tetrahymena cytoplasm contains granular/globular-structures of TpCCT-subunits in close association with microtubule arrays. Studies of reciliation and with cycloheximide suggest that these structures may be sites of translation and folding. Combined biochemical techniques revealed that reciliation affects the oligomeric state of TpCCT-subunits being tubulin preferentially associated with smaller CCT oligomeric species in early stages of reciliation. Collectively, these findings indicate that the oligomeric state of CCT-subunits reflects the translation capacity of the cell and microtubules integrity.
Peer review: yes
URI: http://hdl.handle.net/10400.21/3046
ISSN: 1090-2422
Versão do Editor: http://www.sciencedirect.com/science/article/pii/S0014482703003252
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