Journal of cell science · 2006
Tuba stimulates intracellular N-WASP-dependent actin assembly.
СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Kovacs Eva M, Makar Robert S, Gertler Frank B
Аннотация
Tuba is a multidomain scaffolding protein that links cytoskeletal dynamics and membrane trafficking pathways. The N-terminus of Tuba binds dynamin1, and the C-terminus contains domains that can interact with signaling pathways and cytoskeletal regulatory elements. We investigated Tuba localization, distribution and function in B16 melanoma cells. Tuba overexpression stimulated dorsal ruffles that occurred independently of dynamin function. Tuba expression induced actin-driven motility of small puncta that required the C-terminal SH3, GEF and BAR domains. Additionally, Tuba was recruited to lipid vesicles generated by overexpression of phosphatidylinositol-4-phosphate 5-kinase type Ialpha (PIP5Kalpha), localizing prominently to the head of the comets and at lower levels along the actin tail. We propose that Tuba facilitates dorsal ruffling of melanoma cells through direct interaction with actin-regulatory proteins and the recruitment of signaling molecules to lipid microdomains for the coordinated assembly of a cytoskeletal network. Knockdown of Tuba by RNA interference (RNAi) attenuated PIP5Kalpha-generated comet formation and the invasive behavior of B16 cells, implying that Tuba function is required for certain aspects of these processes. These results suggest first that Tuba-stimulated dorsal ruffling might represent a novel mechanism for the coordination of N-WASP-dependent cytoskeletal rearrangements and second that Tuba function is implicated in motility processes.
Предметные рубрики MeSH
Actin-Related Protein 2-3 ComplexActinsAnimalsCarrier ProteinsCell Adhesion MoleculesCell MembraneCell Membrane StructuresCell MovementCells, CulturedCortactinCytoskeletal ProteinsFibronectinsGene SilencingGrowth SubstancesMelanoma, ExperimentalMiceMinor Histocompatibility AntigensNeoplasm InvasivenessPhosphotransferases (Alcohol Group Acceptor)Protein IsoformsProtein Structure, TertiaryRNA, Small InterferingTissue DistributionTransfectionTubulinWiskott-Aldrich Syndrome Protein, Neuronalcdc42 GTP-Binding Protein