نتایج جستجو برای: interphase microtubule damage response

تعداد نتایج: 1200566  

2010
Neus Teixidó-Travesa Judit Villén Cristina Lacasa Maria Teresa Bertran Marco Archinti Steven P. Gygi Carme Caelles Joan Roig Jens Lüders

The γ-tubulin complex is a multi-subunit protein complex that nucleates microtubule polymerization. γ-Tubulin complexes are present in all eukaryotes, but size and subunit composition vary. In Drosophila, Xenopus, and humans large γ-tubulin ring complexes (γTuRCs) have been described, which have a characteristic open ring-shaped structure and are composed of a similar set of subunits, named γ-t...

Journal: :Molecular and cellular biology 2005
Hyekyung P Cho Yie Liu Marla Gomez John Dunlap Mike Tyers Yisong Wang

The Cdc14 dual-specificity phosphatases regulate key events in the eukaryotic cell cycle. However, little is known about the function of mammalian CDC14B family members. Here, we demonstrate that subcellular localization of CDC14B protein is cell cycle regulated. CDC14B can bind, bundle, and stabilize microtubules in vitro independently of its catalytic activity. Basic amino acid residues withi...

Journal: :Molecular biology of the cell 2006
Nathalie Colombié Christel Vérollet Paula Sampaio André Moisand Claudio Sunkel Henri-Marc Bourbon Michel Wright Brigitte Raynaud-Messina

Gamma-tubulin, a protein critical for microtubule assembly, functions within multiprotein complexes. However, little is known about the respective role of gamma-tubulin partners in metazoans. For the first time in a multicellular organism, we have investigated the function of Dgrip84, the Drosophila orthologue of the Saccharomyces cerevisiae gamma-tubulin-associated protein Spc97p. Mutant analy...

2010
Jie Zhu Anton Burakov Vladimir Rodionov Alex Mogilner

The centrosome position in many types of interphase cells is actively maintained in the cell center. Our previous work indicated that the centrosome is kept at the center by pulling force generated by dynein and actin flow produced by myosin contraction and that an unidentified factor that depends on microtubule dynamics destabilizes position of the centrosome. Here, we use modeling to simulate...

Journal: :Cell 2010
Sarah S. Goodwin Ronald D. Vale

Tubulin assembles into microtubule polymers that have distinct plus and minus ends. Most microtubule plus ends in living cells are dynamic; the transitions between growth and shrinkage are regulated by assembly-promoting and destabilizing proteins. In contrast, minus ends are generally not dynamic, suggesting their stabilization by some unknown protein. Here, we have identified Patronin (also k...

2016
Juan Manuel Gomez Lyubov Chumakova Natalia A Bulgakova Nicholas H Brown

Interphase microtubule organization is critical for cell function and tissue architecture. In general, physical mechanisms are sufficient to drive microtubule organization in single cells, whereas cells within tissues are thought to utilize signalling mechanisms. By improving the imaging and quantitation of microtubule alignment within developing Drosophila embryos, here we demonstrate that mic...

Journal: :PLoS Biology 2007
Philipp Niethammer Iva Kronja Stefanie Kandels-Lewis Sonja Rybina Philippe Bastiaens Eric Karsenti

The cytoplasm of eukaryotic cells is thought to adopt discrete "states" corresponding to different steady states of protein networks that govern changes in subcellular organization. For example, in Xenopus eggs, the interphase to mitosis transition is induced solely by activation of cyclin-dependent kinase 1 (CDK1) that phosphorylates many proteins leading to a reorganization of the nucleus and...

Journal: :Molecular biology of the cell 2005
Itaru Samejima Paula C C Lourenço Hilary A Snaith Kenneth E Sawin

From an insertional mutagenesis screen, we isolated a novel gene, mto2+, involved in microtubule organization in fission yeast. mto2Delta strains are viable but exhibit defects in interphase microtubule nucleation and in formation of the postanaphase microtubule array at the end of mitosis. The mto2Delta defects represent a subset of the defects displayed by cells deleted for mto1+ (also known ...

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