Clathrin-mediated endocytosis (CME) is a major route by which cells take up many nutrients and regulatory molecules and down-regulate membrane proteins in response to their ligands and environmental signals. Further importance of this pathway is exemplified by a number of human diseases that are associated with CME, including cancer, cardiovascular and neurological disorders, and entry of infectious viruses into cells. While many factors involved in CME have been identified and a large number of protein- protein or protein-lipid interactions for them have been described, assigning specific roles to these proteins remains a challenge to the field. There is still much to learn about how cargo are collected, the importance of the elaborate network of interactions and scaffolding functions of the endocytic machinery, how force is generated to invaginate and pinch off a vesicle, and how the timing and regulation of assembly and disassembly of these components coordinates this dynamic process. Moreover, aside from phosphoinositides, little is known about lipid requirements for formation of an endocytic vesicle. Studies in this lab have combined live cell imaging analysis with biochemistry, cell biology and the powerful molecular genetics methods of S. cerevisiae to study the endocytic process. In yeast, as in all eukaryotes, both clathrin and the actin cytoskeleton are critical for endocytosis. Furthermore, most endocytic factors identified in yeast have conserved counterparts in animal cells that are involved in CME. Work from several labs, including ours, has clearly validated yeast as an important model for discovering how this large "molecular machine" drives the internalization process. In this project we continue our efforts to dissect the roles of components of the endocytic machinery using the yeast system. We focus primarily on the novel F-BAR family of FCHO1/2 proteins (Syp1 in yeast), the role of clathrin light chain and regulation of its binding partner Sla2 (related to Hip1/R proteins in animl cells), and the roles of lipids in generating an endocytic vesicle. These studies will provide new insight into the mechanisms of endocytosis and vesicle formation during membrane transport in general.
Clathrin mediated endocytosis is a principal pathway for internalization of many important cellular components, such as lipids, iron, immunoglobulins, many receptors, and viruses. It plays a key role in cell communication, hormone regulation, cell polarity, immune response, growth and development. Therefore, unraveling the roles of the many components involved in endocytosis, including the membrane lipid composition needed, has relevance for diverse human diseases, including cancer, diabetes, cardiovascular disease, neurological disorders, and bacterial and viral infection.
|Mukherjee, Debarati; Sen, Arpita; Boettner, Douglas R et al. (2013) Bem3, a Cdc42 GTPase-activating protein, traffics to an intracellular compartment and recruits the secretory Rab GTPase Sec4 to endomembranes. J Cell Sci 126:4560-71|
|Boettner, Douglas R; Chi, Richard J; Lemmon, Sandra K (2012) Lessons from yeast for clathrin-mediated endocytosis. Nat Cell Biol 14:2-10|
|Boettner, Douglas R; Friesen, Helena; Andrews, Brenda et al. (2011) Clathrin light chain directs endocytosis by influencing the binding of the yeast Hip1R homologue, Sla2, to F-actin. Mol Biol Cell 22:3699-714|
|Grotsch, Helga; Giblin, Jonathan P; Idrissi, Fatima-Zahra et al. (2010) Calmodulin dissociation regulates Myo5 recruitment and function at endocytic sites. EMBO J 29:2899-914|
|Collette, John R; Chi, Richard J; Boettner, Douglas R et al. (2009) Clathrin functions in the absence of the terminal domain binding site for adaptor-associated clathrin-box motifs. Mol Biol Cell 20:3401-13|
|Boettner, Douglas R; D'Agostino, Jessica L; Torres, Onaidy Teresa et al. (2009) The F-BAR protein Syp1 negatively regulates WASp-Arp2/3 complex activity during endocytic patch formation. Curr Biol 19:1979-87|
|Newpher, Thomas M; Idrissi, Fatima-Zahra; Geli, Maria Isabel et al. (2006) Novel function of clathrin light chain in promoting endocytic vesicle formation. Mol Biol Cell 17:4343-52|
|Chang, Ji Suk; Henry, Kenneth; Geli, Maria Isabel et al. (2006) Cortical recruitment and nuclear-cytoplasmic shuttling of Scd5p, a protein phosphatase-1-targeting protein involved in actin organization and endocytosis. Mol Biol Cell 17:251-62|
|Newpher, Thomas M; Smith, Robin P; Lemmon, Vance et al. (2005) In vivo dynamics of clathrin and its adaptor-dependent recruitment to the actin-based endocytic machinery in yeast. Dev Cell 9:87-98|
|Henry, Kenneth R; D'Hondt, Kathleen; Chang, Ji Suk et al. (2003) The actin-regulating kinase Prk1p negatively regulates Scd5p, a suppressor of clathrin deficiency, in actin organization and endocytosis. Curr Biol 13:1564-9|
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