Changes in the cellular carbohydrate metabolism are a hallmark of malignant transformation and represent one of the earliest discernible events in tumorigenesis. In the early stages of certain epithelial cancers, a metabolic switch is regularly observed, in which slowly growing glycogenotic cells are converted to highly proliferating basophilic cells. This step is accompanied by a rapid depletion of the intracellular glycogen stores, which in liver carcinogenesis results from the activation of the enzyme acid α- glucosidase by an as yet unknown mechanism. We show here that acid α- glucosidase is a target for the E7 protein encoded by human papillomavirus type 16, a human tumor virus that plays a key role in the genesis of cervical carcinoma. We show that expression of E7 induces the catalytic activity of acid α-glucosidase in vivo and wild type E7, but not transformation- deficient mutants bind directly to acid α-glucosidase and increase the catalytic activity of the enzyme in vitro. The data suggest that the E7 protein encoded by human papillomavirus type 16 can act as an allosteric activator of acid α-glucosidase.

doi.org/10.1074/jbc.275.13.9534, hdl.handle.net/1765/57762
Journal of Biological Chemistry
Department of Clinical Genetics

Zwerschke, W., Mannhardt, B., Massimi, P., Nauenburg, S., Pim, D., Nickel, W., … Jansen-Dürr, P. (2000). Allosteric activation of acid α-glucosidase by the human papillomavirus E7 protein. Journal of Biological Chemistry, 275(13), 9534–9541. doi:10.1074/jbc.275.13.9534