The endoplasmic reticulum (ER) has an elaborate and dynamic architecture. This architecture is determined by multiple converging factors and forces including: membrane shaping proteins, dynamics on the cytoskeleton, and abundant contact sites that occur between the ER and other organelles. The result of this interplay is that the ER membrane is spread throughout the cytoplasm as a continuous membrane network made up of multiple functional and structural domains. How different domains can be generated and maintained within a continuous membrane bilayer is the focus of our work. To complement these questions, we also aim to understand the functions of different ER domains and the purpose of ER tubule dynamics. I previously demonstrated that a class of abundant and highly conserved integral membrane shaping proteins, the reticulons, functions to stabilize the structure of peripheral ER tubules in eukaryotes9. However, little is known about how reticulon membrane shaping activities are regulated during ER dynamics. We hypothesize that reticulon oligomerization and/or reversible phosphorylation are two testable and reasonable possible mechanisms for regulating reticulon function. We are also studying how new ER tubules are generated by dynamics on microtubules. Towards this goal, we recently identified a new factor Rab10 that localizes to a dynamic domain at the leading edge of dynamic ER tubules8. Our next goal is to understand how Rab10 dynamic domains are formed and regulated. Finally, we have recently shown that the ER tubules circumscribe mitochondria at the site of mitochondrial division17.
We aim to study the mechanisms and factors that drive ER contact and mitochondrial constriction and subsequent division at these positions.
Very little is known about how the structures of membrane-bound organelles are generated. We are studying how the elaborate shape of the ER is generated and maintained. We have identified factors that regulate ER shape (reticulons) and ER dynamics (Rab10). We aim to identify how these factors are regulated. We have also identified new potential roles of ER tubules at contact sites with other organelles. Specifically, we showed that ER tubules mark the site of mitochondrial division. These data suggest that ER tubules are regulating the biogenesis of another organelle. We will continue to study how ER tubules regulate mitochondrial biogenesis at contact sites and what other factors might be involved.
|Lee, Jason E; Westrate, Laura M; Wu, Haoxi et al. (2016) Multiple dynamin family members collaborate to drive mitochondrial division. Nature 540:139-143|
|Phillips, Melissa J; Voeltz, Gia K (2016) Structure and function of ER membrane contact sites with other organelles. Nat Rev Mol Cell Biol 17:69-82|
|Westrate, L M; Lee, J E; Prinz, W A et al. (2015) Form follows function: the importance of endoplasmic reticulum shape. Annu Rev Biochem 84:791-811|
|Rowland, Ashley A; Chitwood, Patrick J; Phillips, Melissa J et al. (2014) ER contact sites define the position and timing of endosome fission. Cell 159:1027-1041|
|Friedman, Jonathan R; Dibenedetto, Jared R; West, Matthew et al. (2013) Endoplasmic reticulum-endosome contact increases as endosomes traffic and mature. Mol Biol Cell 24:1030-40|
|English, Amber R; Voeltz, Gia K (2013) Endoplasmic reticulum structure and interconnections with other organelles. Cold Spring Harb Perspect Biol 5:a013227|
|English, Amber R; Voeltz, Gia K (2013) Rab10 GTPase regulates ER dynamics and morphology. Nat Cell Biol 15:169-78|
|Murley, Andrew; Lackner, Laura L; Osman, Christof et al. (2013) ER-associated mitochondrial division links the distribution of mitochondria and mitochondrial DNA in yeast. Elife 2:e00422|
|Rowland, Ashley A; Voeltz, Gia K (2012) Endoplasmic reticulum-mitochondria contacts: function of the junction. Nat Rev Mol Cell Biol 13:607-25|
|Friedman, Jonathan R; Voeltz, Gia K (2011) The ER in 3D: a multifunctional dynamic membrane network. Trends Cell Biol 21:709-17|
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