Evolving catalytic properties of the MLL family SET domain
journal contributionposted on 23.09.2020, 13:44 by Ying Zhang, Anshumali Mittal, James Reid, Stephanie Reich, Steven J Gamblin, Jon R Wilson
Methylation of histone H3 lysine-4 is a hallmark of chromatin associated with active gene expression. The activity of H3K4-specific modification enzymes, in higher eukaryotes the MLL (or KMT2) family, is tightly regulated. The MLL family has six members, each with a specialized function. All contain a catalytic SET domain that associates with a core multiprotein complex for activation. These SET domains segregate into three classes that correlate with the arrangement of targeting domains that populate the rest of the protein. Here we show that, unlike MLL1, the MLL4 SET domain retains significant activity without the core complex. We also present the crystal structure of an inactive MLL4-tagged SET domain construct and describe conformational changes that account for MLL4 intrinsic activity. Finally, our structure explains how the MLL SET domains are able to add multiple methyl groups to the target lysine, despite having the sequence characteristics of a classical monomethylase.
Amino Acid SequenceAnimalsBinding SitesBiocatalysisChromatinCrystallography, X-RayDNA-Binding ProteinsEscherichia coliGene ExpressionHistone-Lysine N-MethyltransferaseHistonesHumansKineticsLysineModels, MolecularMolecular Sequence DataMyeloid-Lymphoid Leukemia ProteinProtein BindingProtein FoldingProtein Structure, SecondaryProtein Structure, TertiaryRecombinant Fusion ProteinsSf9 CellsSpodopteraGamblin U11758422206 Biological Sciences08 Information and Computing Sciences03 Chemical SciencesBiophysics