Induction of Tax I expression in MT-4 cells by 5-azacytidine leads to protein binding in the HTLV-I LTR in vivo

The Tax I trans-activator protein of the human T-cell leukemia virus I (HTL V-I) enhances viral gene expression through enhancer sequences in the viral LTR. These sequences consist of three imperfect 21-bp repeats (TRE-1) and a region between the promoter central and promoter proximal TRE-1 (known as TRE-2). We have previously described the in vivo footprint oi the HTLV-I T RE-1s and TRE-2 in two HTLV-I-infected cell lines, MT-2 and MT-4. MT-2 is a high-level producer of virus and shows significant DNA-protein interaction s within the TRE-1s and TRE-2. In contrast, the proviral DNA in MT-4 cells is heavily methylated and produces no detectable virus. In this report, we describe the footprints of the TRE-1s and TRE-2 in MT-4 cells that were ind uced to express high levels of viral proteins by treatment with 5-azacytidi ne, a potent inhibitor of methylation. The footprints of the IRE-is in 5-az acytidine-treated MT-4 cells were virtually identical to those observed in MT-2 cells. In contrast, the footprints within the TRE-2 region of 5-azacyt idine-treated MT-4 cells did not resemble those in either MT-2 or MT-4 cell s, (C) 2001 Academic Press.