TAC-1 and ZYG-9 form a complex that promotes microtubule assembly in C. elegans embryos
BACKGROUND: Modulation of microtubule dynamics is crucial for proper cell division. While a large body of work has made important contributions to our understanding of the mechanisms governing microtubule dynamics in vitro, much remains to be learned about how these mechanisms operate in vivo. RESULTS: We identified TAC-1 as the sole TACC (Transforming Acidic Coiled Coil) protein in C. elegans. TAC-1 consists essentially of a TACC domain, in contrast to the much larger members of this protein family in other species. We find that tac-1 is essential for pronuclear migration and spindle elongation in one-cell-stage C. elegans embryos. Using an in vivo FRAP-based assay, we establish that inactivation of tac-1 results in defective microtubule assembly. TAC-1 is present in the cytoplasm and is enriched at centrosomes in a cell cycle-dependent manner. Centrosomal localization is independent of microtubules but requires the activity of gamma-tubulin and the Aurora-A kinase AIR-1. By conducting FRAP analysis in embryos expressing GFP-TAC-1, we find that centrosomal TAC-1 exchanges rapidly with the cytoplasmic pool. Importantly, we establish that TAC-1 physically interacts with ZYG-9, a microtubule-associated protein (MAP) of the XMAP215 family, both in vitro and in vivo. Furthermore, we also uncover that TAC-1 and ZYG-9 stabilize each other in C. elegans embryos. CONCLUSIONS: Our findings identify TAC-1 as a core structural and functional member of the evolutionarily conserved TACC family of proteins and suggest that mutual stabilization between TACC and XMAP215 proteins is a key feature ensuring microtubule assembly in vivo.
- URL: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=12956950
Keywords: Animals ; Blotting ; Western ; Caenorhabditis elegans/*embryology/metabolism ; Chromosome Mapping ; Comparative Study ; Fluorescence Recovery After Photobleaching ; Fluorescent Antibody Technique ; Microscopy ; Confocal ; Microtubule-Associated Proteins/*metabolism ; Microtubules/*metabolism ; Mitotic Spindle Apparatus/*metabolism ; Precipitin Tests ; RNA Interference ; Research Support ; Non-U.S. Gov't
Swiss Institute for Experimental Cancer Research (ISREC), CH-1066, Epalinges/Lausanne, Switzerland. 0960-9822 (Print) Journal Article
Record created on 2006-08-24, modified on 2016-08-08