The Drosophila kinesin-like protein KLP67A is essential for mitotic and male meiotic spindle assembly
Doxsey, Stephen J.
Pereira, Andrea J.
UMass Chan AffiliationsProgram in Molecular Medicine
Department of Molecular Genetics and Microbiology
Document TypeJournal Article
Mitotic Spindle Apparatus
RNA, Small Interfering
Medicine and Health Sciences
MetadataShow full item record
AbstractWe have performed a mutational analysis together with RNA interference to determine the role of the kinesin-like protein KLP67A in Drosophila cell division. During both mitosis and male meiosis, Klp67A mutations cause an increase in MT length and disrupt discrete aspects of spindle assembly, as well as cytokinesis. Mutant cells exhibit greatly enlarged metaphase spindle as a result of excessive MT polymerization. The analysis of both living and fixed cells also shows perturbations in centrosome separation, chromosome segregation, and central spindle assembly. These data demonstrate that the MT plus end-directed motor KLP67A is essential for spindle assembly during mitosis and male meiosis and suggest that the regulation of MT plus-end polymerization is a key determinant of spindle architecture throughout cell division.
SourceMol Biol Cell. 2004 Jan;15(1):121-31. Epub 2003 Sep 17. Link to article on publisher's site
Permanent Link to this Itemhttp://hdl.handle.net/20.500.14038/38516
Related ResourcesLink to Article in PubMed