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.
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CITATION STYLE
Ali, I., Ramage, H., Boehm, D., Dirk, L. M. A., Sakane, N., Hanada, K., … Ott, M. (2016). The HIV-1 Tat protein is monomethylated at lysine 71 by the lysine methyltransferase KMT7. Journal of Biological Chemistry, 291(31), 16240–16248. https://doi.org/10.1074/jbc.M116.735415
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