_-Catenin is an important protein for cancer research as it influences numerous events in the cell that lead to the development of cancer when gone awry. At the adherens junctions, _-catenin... Show more_-Catenin is an important protein for cancer research as it influences numerous events in the cell that lead to the development of cancer when gone awry. At the adherens junctions, _-catenin functions in cell-cell adhesion to maintain epithelial organisation. As an effector of Wnt signaling, _-catenin controls numerous developmental processes as well as homeostatic self-renewal. The effector function of _-catenin is to form a transcriptional complex in the nucleus with TCF/Lef transcription factors to regulate target gene expression. Due to the dual function of _-catenin in cell adhesion and signaling, there are different pools of the protein. The research described in this thesis focuses on the role of _-catenin in the Wnt signaling pathway. What is the pool of _-catenin that is active in signaling? Where is active _-catenin localized? Where and how is _-catenin activated and how is its nuclear export regulated to terminate Wnt signaling. Chapter 1 provides a general introduction about the different aspects of nuclear transport and the Wnt signaling cascade, putting it into the context of cancer development. Chapter 2 describes the identification of Ran-binding protein 3 (RanBP3) as a novel regulator of the active signaling form of _-catenin. We initiated this study to investigate the nuclear translocation of _-catenin and found that RanBP3 directly inhibits _-catenin signaling by stimulating nuclear export of the transcriptionally active form of _-catenin. The active form of _-catenin is unphosphorylated on its N-terminus, and covers only a small fraction of the total amount of _-catenin in the cell. We therefore continued to study the localization of this pool of _-catenin in Chapter 3. We describe that a relative large pool of unphosphorylated _-catenin resides at the adherens junctions, where it most likely functions in cell-cell adhesion. As Wnt treatment induces recruitment of unphosphorylated _-catenin to the plasma membrane, it is impossible to distinguish the resident junctional pool of unphosphorylated _-catenin from the signaling pool. We emphasize the importance of an E-cadherin null background in studying signaling competent unphosphorylated _-catenin. In Chapter 4, we study the unphosphorylated _-catenin pool at the plasma membrane upon Wnt signal induction in E-cadherin knock out cells. Plasma membrane recruitment of _-catenin in the early steps of the Wnt signaling cascade fits with recent new insights, which suggest recruitment of Axin and Dvl to the activated Wnt receptor LRP5/6. We expand these insights by showing that active _-catenin, Axin, APC and activated LRP6 receptor all localize to the plasma membrane upon Wnt stimulation. Moreover, we find that Wnt induced _-catenin is transcriptionally more active than overexpressed _-catenin. We suggest a model in which plasma membrane recruitment of _-catenin represents an important step in _-catenin processing and Wnt signal transduction. In Chapter 5, we determine the nuclear export kinetics of _-catenin in human cells and show that _-catenin exits the nucleus very fast, independently of the CRM1 export pathway and that _-catenin can enhance export of the small molecule GFP (green fluorescent protein). These observations fit into a model in which _-catenin can translocate quickly into and out of the nucleus independently of nuclear transport receptors. Therefore, the activity and localization of _-catenin are likely to be regulated by retention of the protein in the nucleus, cytoplasm and plasma membrane. Finally, in Chapter 6 we reconcile our findings with current knowledge of the Wnt signaling cascade. Show less
The nuclear pore complex (NPC) is the gateway to and from the genome. The work presented in this thesis is the result of the investigations towards understanding some of the key questions affecting... Show moreThe nuclear pore complex (NPC) is the gateway to and from the genome. The work presented in this thesis is the result of the investigations towards understanding some of the key questions affecting NPC biology: How is the NPC built up? Can we dissect different modes of transport at the level of the NPC? Does the NPC play a role in the development of cancer? Several findings presented in this thesis have contributed to the current knowledge of the biology of the Nuclear Pore Complex. Structurally, the hierarchy towards incorporation to the NPC of the cytoplasmic components Nup88, Nup214 and Nup 358 and their relevance to nuclear transport has been established. Concerning nuclear transport itself, a supporting role in CRM1-mediated export has been assigned to Nup358 and an explanation to the weak nature of the interaction of CRM1 and its NES-containing cargoes been elucidated. This work has amplified as well the concept of nuclear translocation by creating a distinction in transport pathways that, instead of been exclusively dependent on the receptor-NPC and the receptor-cargo interactions, consider the characteristics of the cargo itself. In fact , while showing cargos that can be exported by CRM1 independently of Nup214, we present first in vivo evidence of the implication of Nup214 in a NPC gating mechanism for the CRM1-dependent export of preribosomes Furthermore, this result excludes any implication of the strong CRM1 binding Nup214 FG-domain in this mechanism and in other suggested models of CRM1 export. Finally, this thesis has provided information concerning the localization and stability of the aberrant product Nup214-ABL that may be of great value for the development of alternative therapies of leukemic diseases Show less
