Document Type
Article
Publication Date
11-13-2015
Publication Title
ELife
Department
Geisel School of Medicine
Abstract
Recognition and elimination of tumor cells by the immune system is crucial for limiting tumor growth. Natural killer (NK) cells become activated when the receptor NKG2D is engaged by ligands that are frequently upregulated in primary tumors and on cancer cell lines. However, the molecular mechanisms driving NKG2D ligand expression on tumor cells are not well defined. Using a forward genetic screen in a tumor-derived human cell line, we identified several novel factors supporting expression of the NKG2D ligand ULBP1. Our results show stepwise contributions of independent pathways working at multiple stages of ULBP1 biogenesis. Deeper investigation of selected hits from the screen showed that the transcription factor ATF4 drives ULBP1 gene expression in cancer cell lines, while the RNA-binding protein RBM4 supports ULBP1 expression by suppressing a novel alternatively spliced isoform of ULBP1 mRNA. These findings offer insight into the stress pathways that alert the immune system to danger.
DOI
10.7554/eLife.08474
Dartmouth Digital Commons Citation
Gowen, Benjamin G; Chim, Bryan; Marceau, Caleb D.; Greene, Trever T; Burr, Patrick; Gonzalez, Jeanmarie R.; Hesser, Charles; Dietzen, Peter A.; Russell, Teal; Iannello, Alexandre; Coscoy, Laurent; and Sentman, Charles L., "A Forward Genetic Screen Reveals Novel Independent Regulators of Ulbp1, an Activating Ligand for Natural Killer Cells" (2015). Dartmouth Scholarship. 2496.
https://digitalcommons.dartmouth.edu/facoa/2496
