Genetic Dissection of Yeast Bax Inhibitor Function in UPR and Calcium Signaling

点击翻译按钮获取中文摘要

DESCRIPTION (provided by applicant): Bax inhibitor-1 (BI-1) is a six-transmembrane containing endoplasmic reticulum (ER) resident protein that provides cytoprotective functions in both animals and plants. It is up regulated in a variety of different human tumors like anaplastic large cell lymphoma, prostate and breast carcinoma, and acute myeloid leukemia. The precise biological function of Bax inhibitor remains unclear. In mammalian cells, several studies conclude that BI-1 may protect cells from ER-stress induced programmed cell death (PCD) by suppressing the signaling of the unfolded protein response (UPR). It also appears to regulate the concentration of Ca2+ in the ER and the cytosol. Despite these published studies, however, it is still not clear whether (and if it is, how) Bax inhibitor's role in the regulation of the UPRis linked to its role in the regulation of cellular calcium levels. Therefore there is a need to answe a pressing question in the field: Does Bax inhibitor regulate cellular calcium levels by regulating the UPR (or vice versa) or does it accomplish these functions independently? To fill this knowledge gap, my laboratory at Providence College initiated now-published studies to investigate the function of the Saccharomyces cerevisiae Bax inhibitor homolog, which we have called BXI1. In this R15 AREA proposal, we describe genetic - primarily epistatic - experiments that build upon our published data to continue to use the power of yeast genetics to characterize the link between the two functions of Bax inhibitor, the regulation of the UPR and the regulation of calcium signaling. We expect our research program to have a positive impact because these genetic studies should help us not only to better understand Bax inhibitor function in programmed cell death and cancer but also to uncover functional links between the UPR and calcium signaling. Since ER stress and the UPR have been implicated in a variety of human diseases we anticipate that our research program should have a positive impact on fields exploring the biological basis for these and other diseases that involve ER stress and the UPR. Finally, in addition to expanding our knowledge base in ER-stress and cancer more generally and in Bax inhibitor's mechanism of action more specifically, funding the research described in this AREA R15 grant proposal will also allow my laboratory and our department here at Providence College to improve our research infrastructure so that we can continue to train and to prepare talented undergraduate students for successful careers in the biomedical sciences.