Source:http://linkedlifedata.com/resource/pubmed/id/17666432
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
Pt 16
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pubmed:dateCreated |
2007-8-10
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pubmed:abstractText |
The early Caenorhabditis elegans embryo is well suited for investigating microtubule-dependent cell division processes. In the one-cell stage, the XMAP215 homologue ZYG-9, associated with the TACC protein TAC-1, promotes microtubule growth during interphase and mitosis, whereas the doublecortin domain protein ZYG-8 is required for anaphase spindle positioning. How ZYG-9, TAC-1 and ZYG-8 together ensure correct microtubule-dependent processes throughout the cell cycle is not fully understood. Here, we identify new temperature-sensitive alleles of zyg-9 and tac-1. Analysis of ZYG-9 and TAC-1 distribution in these mutants identifies amino acids important for centrosomal targeting and for stability of the two proteins. This analysis also reveals that TAC-1 is needed for correct ZYG-9 centrosomal enrichment. Moreover, we find that ZYG-9, but not TAC-1, is limiting for microtubule-dependent processes in one-cell-stage embryos. Using two of these alleles to rapidly inactivate ZYG-9-TAC-1 function, we establish that this complex is required for correct anaphase spindle positioning. Furthermore, we uncover that ZYG-9-TAC-1 and ZYG-8 function together during meiosis, interphase and mitosis. We also find that TAC-1 physically interacts with ZYG-8 through its doublecortin domain, and that in vivo TAC-1 and ZYG-8 are part of a complex that does not contain ZYG-9. Taken together, these findings indicate that ZYG-9-TAC-1 and ZYG-8 act in a partially redundant manner to ensure correct microtubule assembly throughout the cell cycle of early C. elegans embryos.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Caenorhabditis elegans Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Cell Cycle Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/ZYG-9 protein, C elegans,
http://linkedlifedata.com/resource/pubmed/chemical/ZYG8 protein, C elegans
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0021-9533
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
120
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2963-73
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pubmed:meshHeading |
pubmed-meshheading:17666432-Alleles,
pubmed-meshheading:17666432-Anaphase,
pubmed-meshheading:17666432-Animals,
pubmed-meshheading:17666432-Caenorhabditis elegans,
pubmed-meshheading:17666432-Caenorhabditis elegans Proteins,
pubmed-meshheading:17666432-Cell Cycle,
pubmed-meshheading:17666432-Cell Cycle Proteins,
pubmed-meshheading:17666432-Embryo, Nonmammalian,
pubmed-meshheading:17666432-Embryo Loss,
pubmed-meshheading:17666432-Microtubules,
pubmed-meshheading:17666432-Mitotic Spindle Apparatus,
pubmed-meshheading:17666432-Mutation,
pubmed-meshheading:17666432-Phenotype,
pubmed-meshheading:17666432-Protein Binding,
pubmed-meshheading:17666432-Protein Structure, Tertiary
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pubmed:year |
2007
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pubmed:articleTitle |
ZYG-9, TAC-1 and ZYG-8 together ensure correct microtubule function throughout the cell cycle of C. elegans embryos.
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pubmed:affiliation |
Swiss Institute for Experimental Cancer Research (ISREC), Swiss Federal Institute of Technology (EPFL), School of Life Sciences, Lausanne, Switzerland.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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