This project is focused on understanding clathrin-independent forms of endocytosis (CIE). Endocytosis that occurs without clathrin coats occurs in all cells but is poorly understood. We are interested in studying the cargo proteins that enter cells by this mechanism, their intracellular itinerary once they have been internalized and whether they contain amino acid sequences that allow for specialized sorting within cells. We have been identifying new cargo proteins and found that a subset of these proteins take alternative traffic routes once they have entered cells. The major histocompatibility complex Class I protein (MHCI), is a prototypical clathrin-indepenent cargo protein and after internalization it reaches endosomes that contain cargo proteins such as the transferrin receptor that enter via clathrin-depenent endocytosis. From there, MHCI travels either to late endosomes and lysosomes where it is degraded or on to recycling tubules that return MHCI back to the cell surface. CD44, CD98, and CD147, however, show an altered itinerary in many cells where they traffic directly into the recycling tubules and avoid trafficking to lysosomes. Consistent with this altered itinerary, CD44, CD98 and CD147 are long-lived proteins and are not degraded like MHCI, which is routed to lysosomes. We are interested in the role that ubiquitin modification of cargo proteins plays in regulating the sorting of cargo and routing of cargo to lysosomes for degradation. We previously showed that over expression of the MARCH8 E3 ubiquitin ligase leads to ubiquitination and degradation of CD98, normally a long-lived protein (Eyster et al 2011). We now show that expression of a de-ubiquitinase (DUB) or ubiquitin-specific protease (USP) can counteract the effect of expression of MARCH8. This DUB is called TRE17/USP6 and was previously shown to be unregulated in ABC bone cancer. Expression of TRE17 specifically de-ubiquitinates CD98 and returns its trafficking to the normal pathway (i.e. avoidance of lysosomes) (Funakoshi et al, 2014). However TRE17 did not rescue the effect of MARCH8 on degradation of the transferrin receptor. As a follow-up to this study, we have set-up an siRNA screen of de-ubiquitinases (DUBs), knocking down the 100 DUBs in the human genome to identify those DUBs that, in addition to TRE17 (USP6), are responsible for protecting CD98 and CD147 from lysosomal degradation. This screen is currently on-going.
| Zeltzer, Sebastian; Zeltzer, Carol A; Igarashi, Suzu et al. (2018) Virus Control of Trafficking from Sorting Endosomes. MBio 9: |
| Johnson, Debra L; Wayt, Jessica; Wilson, Jean M et al. (2017) Arf6 and Rab22 mediate T cell conjugate formation by regulating clathrin-independent endosomal membrane trafficking. J Cell Sci 130:2405-2415 |
| Donaldson, Julie G; Johnson, Debra L; Dutta, Dipannita (2016) Rab and Arf G Proteins in Endosomal Trafficking & Cell Surface Homeostasis. Small GTPases :0 |
| Donaldson, Julie G (2015) Immunofluorescence Staining. Curr Protoc Cell Biol 69:4.3.1-7 |
| Funakoshi, Yuji; Chou, Margaret M; Kanaho, Yasunori et al. (2014) TRE17/USP6 regulates ubiquitylation and trafficking of cargo proteins that enter cells by clathrin-independent endocytosis. J Cell Sci 127:4750-61 |
| Karabasheva, Darya; Cole, Nelson B; Donaldson, Julie G (2014) Roles for trafficking and O-linked glycosylation in the turnover of model cell surface proteins. J Biol Chem 289:19477-90 |
| Porat-Shliom, Natalie; Weigert, Roberto; Donaldson, Julie G (2013) Endosomes derived from clathrin-independent endocytosis serve as precursors for endothelial lumen formation. PLoS One 8:e81987 |
| Maldonado-Báez, Lymarie; Williamson, Chad; Donaldson, Julie G (2013) Clathrin-independent endocytosis: a cargo-centric view. Exp Cell Res 319:2759-69 |
| Maldonado-Báez, Lymarie; Cole, Nelson B; Krämer, Helmut et al. (2013) Microtubule-dependent endosomal sorting of clathrin-independent cargo by Hook1. J Cell Biol 201:233-47 |
| Rosemond, Erica; Rossi, Mario; McMillin, Sara M et al. (2011) Regulation of M? muscarinic receptor expression and function by transmembrane protein 147. Mol Pharmacol 79:251-61 |
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