Papillomaviruses are small, ubiquitous DNA viruses that infect a variety of keratinizing and mucosal epithelia. While all HPVs produce benign lesions, a small subset of high risk (HR) HPVs cause lesions that can progress to cancer. A hallmark of nearly all cancers is that they have activated an enzyme, telomerase, which maintains the repetitive DNA sequences at the end of chromosomes, allowing tumor cells to replicate indefinitely. We have shown that the HR HPV E6 proteins directly activate the expression of the catalytic subunit of telomerase, hTERT. E6 coordinates the recruitment of transcriptional activators and elimination of repressors at the hTERT promoter, and further enhances TERT levels through post-transcriptional means. The overall goal of this application is to continue to explore the mechanisms by which HR HPV E6 proteins regulate telomerase activity, to determine whether these mechanisms are unique to HPV or play a role in other cancers, to explore the benefit of hTERT activation to the HPV lifecycle, and to determine whether telomerase-independent activities of hTERT influence the biology of HPVs. Our specific aims are 1) To characterize mechanisms by which E6 regulates hTERT transcription. We will focus on candidates obtained in a novel screen for which there are predicted binding sites in the -725 to +61 bp promoter. Additional candidates predicted to bind but not found in the screen will be tested. We propose to determine the mechanisms by which E6 affects the recruitment or elimination of these factors 2. To examine the generalizability of hTERT regulation by E6. We propose to examine a set of transcriptional activators and repressors shown to regulate hTERT in HPV E6 -HFKs in a variety of non-HPV tumor cell lines. 3. To determine the role of hTERT in the HPV lifecycle. To determine whether HPVs require hTERT for some stage in their lifecycle we will knockdown hTERT in cells into which the entire HPV genome has been transfected. Using both proliferative and differentiation-promoting growth conditions we will measure episome maintenance, viral DNA amplification, late gene expression, and epithelial differentiation. 4. To determine if telomerase-independent functions of hTERT affect the HPV lifecycle. First, we will determine whether induction of TERT is linked to Wnt signaling in HFKs and whether Wnt signaling is important for the HPV lifecycle. Secondly, we will explore the new finding that TERT associates with RMRP RNA, which is processed into siRNAs. We will test the hypothesis that siRNAs generated by this complex regulate critical features of HPV expressing cells.