Abstract

HIV1-TAT interactive protein (TIP60) is a haploinsufficient tumor suppressor. However, the potential mechanisms endowing its tumor suppressor ability remain incompletely understood. It plays a vital role in virus-induced cancers where TIP60 down-regulates the expression of human papillomavirus (HPV) oncoprotein E6 which in turn destabilizes TIP60. This intrigued us to identify the role of TIP60, in the context of a viral infection, where it is targeted by oncoproteins. Through an array of molecular biology techniques such as Chromatin immunoprecipitation, expression analysis and mass spectrometry, we establish the hitherto unknown role of TIP60 in repressing the expression of the catalytic subunit of the human telomerase complex, TERT, a key driver for immortalization. TIP60 acetylates Sp1 at K639, thus inhibiting Sp1 binding to the TERT promoter. We identified that TIP60-mediated growth suppression of HPV-induced cervical cancer is mediated in part due to TERT repression through Sp1 acetylation. In summary, our study has identified a novel substrate for TIP60 catalytic activity and a unique repressive mechanism acting at the TERT promoter in virus-induced malignancies.

Highlights

  • HIV-1 TAT Interactive protein (TIP60) is a lysine acetyltransferase and a member of the MYST (Moz, Ybf2/Sas3, Sas2 and TIP60) family of evolutionarily related histone acetyltransferases [1]

  • TIP60 which is targeted for degradation by human papillomavirus (HPV) oncoprotein E6, acetylates Specificity Protein 1 (Sp1), a positive regulator of TERT

  • We show that TIP60-mediated acetylation of Sp1, inhibits Sp1 function at the TERT promoter, thereby reducing TERT expression and the growth of HPV-positive cervical cancer cells, HeLa

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Summary

Introduction

HIV-1 TAT Interactive protein (TIP60) is a lysine acetyltransferase and a member of the MYST (Moz, Ybf2/Sas, Sas and TIP60) family of evolutionarily related histone acetyltransferases [1]. E6 destabilizes TIP60 by cooperating with an E3 cellular ubiquitin ligase, EDD1 [8], and TIP60 in turn represses the E6 promoter, maintaining a delicate balance of cellular and viral gene expression [7]. Both high and low-risk HPV are capable of destabilizing TIP60 whereas only the high-risk E6 is capable of destabilizing p53. This suggests that TIP60 degradation is an essential and common mechanism in promoting viral gene expression [7, 11]

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