Autoacetylation of the Histone Acetyltransferase Rtt109

Brittany N Albaugh,Kevin M Arnold,Susan Lee,John M Denu

doi:10.1074/jbc.m111.251579

Brittany N Albaugh, Kevin M Arnold + Show 2 more

Open Access

https://doi.org/10.1074/jbc.m111.251579

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Abstract

Rtt109 is a yeast histone acetyltransferase (HAT) that associates with histone chaperones Asf1 and Vps75 to acetylate H3K56, H3K9, and H3K27 and is important in DNA replication and maintaining genomic integrity. Recently, mass spectrometry and structural studies of Rtt109 have shown that active site residue Lys-290 is acetylated. However, the functional role of this modification and how the acetyl group is added to Lys-290 was unclear. Here, we examined the mechanism of Lys-290 acetylation and found that Rtt109 catalyzes intramolecular autoacetylation of Lys-290 ∼200-times slower than H3 acetylation. Deacetylated Rtt109 was prepared by reacting with a sirtuin protein deacetylase, producing an enzyme with negligible HAT activity. Autoacetylation of Rtt109 restored full HAT activity, indicating that autoacetylation is necessary for HAT activity and is a fully reversible process. To dissect the mechanism of activation, biochemical, and kinetic analyses were performed with Lys-290 variants of the Rtt109-Vps75 complex. We found that autoacetylation of Lys-290 increases the binding affinity for acetyl-CoA and enhances the rate of acetyl-transfer onto histone substrates. This study represents the first detailed investigation of a HAT enzyme regulated by single-site intramolecular autoacetylation.

Highlights

3.9 Ϯ 0.5 ϫ 105 9.8 Ϯ 0.9 ϫ 102 1.6 Ϯ 0.3 ϫ 102 1.2 Ϯ 0.3 ϫ 2.7 Ϯ 0.7 ϫ 1.4 Ϯ 0.3 ϫ 101 6 Ϯ 1 ϫ 102 3.8 Ϯ 0.8 ϫ 101 a Standard errors are reported
We evaluated the ability of deacetylated RV to be re-activated by autoacetylation
Re-acetylation recovered full activity, as the rate of histone acetylation (0.36 Ϯ 0.02 sϪ1) of re-acetylated RV was indistinguishable from RV (0.36 Ϯ 0.01 sϪ1) that had never been deacetylated (Fig. 2C). These results indicate that autoacetylation is a reversible process that functions to regulate Rtt[109] HAT activity

Summary

Introduction

3.9 Ϯ 0.5 ϫ 105 9.8 Ϯ 0.9 ϫ 102 1.6 Ϯ 0.3 ϫ 102 1.2 Ϯ 0.3 ϫ 2.7 Ϯ 0.7 ϫ 1.4 Ϯ 0.3 ϫ 101 6 Ϯ 1 ϫ 102 3.8 Ϯ 0.8 ϫ 101 a Standard errors are reported. We observed an expected exponential increase in histone acetylation, reflecting Rtt[109] autoacetylation and subsequent activation of HAT activity (data not shown). To determine if acetylated Lys-290 contributes to substrate binding, acetyl-CoA and H3 peptide saturation curves were performed with K290QRV and K290RRV.

Results

Conclusion