| Literature DB >> 27235396 |
Ibraheem Ali1, Holly Ramage2, Daniela Boehm2, Lynnette M A Dirk3, Naoki Sakane4, Kazuki Hanada5, Sara Pagans2, Katrin Kaehlcke2, Katherine Aull6, Leor Weinberger6, Raymond Trievel7, Martina Schnoelzer8, Masafumi Kamada5, Robert Houtz3, Melanie Ott9.
Abstract
The HIV-1 transactivator protein Tat is a critical regulator of HIV transcription primarily enabling efficient elongation of viral transcripts. Its interactions with RNA and various host factors are regulated by ordered, transient post-translational modifications. Here, we report a novel Tat modification, monomethylation at lysine 71 (K71). We found that Lys-71 monomethylation (K71me) is catalyzed by KMT7, a methyltransferase that also targets lysine 51 (K51) in Tat. Using mass spectrometry, in vitro enzymology, and modification-specific antibodies, we found that KMT7 monomethylates both Lys-71 and Lys-51 in Tat. K71me is important for full Tat transactivation, as KMT7 knockdown impaired the transcriptional activity of wild type (WT) Tat but not a Tat K71R mutant. These findings underscore the role of KMT7 as an important monomethyltransferase regulating HIV transcription through Tat.Entities:
Keywords: human immunodeficiency virus (HIV); post-translational modification (PTM); protein methylation; transcription regulation; viral transcription
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Year: 2016 PMID: 27235396 PMCID: PMC4965572 DOI: 10.1074/jbc.M116.735415
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157