BTG gene expression in the p53-dependent and -independent cellular response to DNA damage

Exposure of mammalian cells to genotoxic agents evokes a complex cellular r esponse. An ordered series of molecular events is necessary to sense DNA da mage, transduce the signal, and ultimately delay the cell cycle or trigger apoptosis. Recently, we have shown that BTG2/TIS21 gene expression was indu ced in response to DNA damage through a p53-dependent pathway. This gene be longs to a newly identified family of structurally related genes whose othe r known human members are BTG1, BTG3, and Tob. To define the respective inv olvement of these four related genes in the cellular response to DNA damage , we studied their expression in human cell lines after a variety of genoto xic treatment. Our results demonstrated that were BTG1, BTG2/TIS21, and Tob genes the DNA damage-inducible genes. However, BTG2/TIS21 appeared to be t he only p53-transcriptional target gene. We speculate that BTG proteins may play a coordinate role in a general transduction pathway that is induced i n response to DNA damage. It has been previously described that recombinant BTG1 and BTG2/TIS21 can physically interact with PRMT1, an arginine methyl transferase, suggesting that BTG1 and BTG2/TIS21 induction may lead to pos ttranslational modifications of cellular proteins. In support of this hypot hesis, we showed that the endogenous induction of BTG1 and BTG2 after genot oxic treatment was correlated with a modulation of protein methylation. (C) 2000 Wiley-Liss, Inc.