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      A comprehensive library of histone mutants identifies nucleosomal residues required for H3K4 methylation

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          Abstract

          Methylation of histone 3 lysine 4 (H3K4) by yeast Set1-COMPASS requires prior monoubiquitination of histone H2B. To define whether other residues within the histones are also required for H3K4 methylation, we systematically generated a complete library of the alanine substitutions of all of the residues of the four core histones in Saccharomyces cerevisiae. From this study we discovered that 18 residues within the four histones are essential for viability on complete growth media. We also identified several cis-regulatory residues on the histone H3 N-terminal tail, including histone H3 lysine 14 (H3K14), which are required for normal levels of H3K4 trimethylation. Several previously uncharacterized trans-regulatory residues on histones H2A and H2B form a patch on nucleosomes and are required for methylation mediated by COMPASS. This library will be a valuable tool for defining the role of histone residues in processes requiring chromatin.

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          Most cited references48

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          Twenty-five years of the nucleosome, fundamental particle of the eukaryote chromosome.

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            How chromatin-binding modules interpret histone modifications: lessons from professional pocket pickers.

            Histones comprise the major protein component of chromatin, the scaffold in which the eukaryotic genome is packaged, and are subject to many types of post-translational modifications (PTMs), especially on their flexible tails. These modifications may constitute a 'histone code' and could be used to manage epigenetic information that helps extend the genetic message beyond DNA sequences. This proposed code, read in part by histone PTM-binding 'effector' modules and their associated complexes, is predicted to define unique functional states of chromatin and/or regulate various chromatin-templated processes. A wealth of structural and functional data show how chromatin effector modules target their cognate covalent histone modifications. Here we summarize key features in molecular recognition of histone PTMs by a diverse family of 'reader pockets', highlighting specific readout mechanisms for individual marks, common themes and insights into the downstream functional consequences of the interactions. Changes in these interactions may have far-reaching implications for human biology and disease, notably cancer.
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              Chromatin modifications by methylation and ubiquitination: implications in the regulation of gene expression.

              It is more evident now than ever that nucleosomes can transmit epigenetic information from one cell generation to the next. It has been demonstrated during the past decade that the posttranslational modifications of histone proteins within the chromosome impact chromatin structure, gene transcription, and epigenetic information. Multiple modifications decorate each histone tail within the nucleosome, including some amino acids that can be modified in several different ways. Covalent modifications of histone tails known thus far include acetylation, phosphorylation, sumoylation, ubiquitination, and methylation. A large body of experimental evidence compiled during the past several years has demonstrated the impact of histone acetylation on transcriptional control. Although histone modification by methylation and ubiquitination was discovered long ago, it was only recently that functional roles for these modifications in transcriptional regulation began to surface. Highlighted in this review are the recent biochemical, molecular, cellular, and physiological functions of histone methylation and ubiquitination involved in the regulation of gene expression as determined by a combination of enzymological, structural, and genetic methodologies.
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                Author and article information

                Journal
                101186374
                31761
                Nat Struct Mol Biol
                Nature structural & molecular biology
                1545-9993
                1545-9985
                16 July 2008
                11 July 2008
                August 2008
                1 February 2009
                : 15
                : 8
                : 881-888
                Affiliations
                Stowers Institute for Medical Research, 1000 East 50th Street, Kansas City, Missouri 64110, USA
                Author notes
                Correspondence should be addressed to A.S. ( ASH@ 123456Stowers-Institute.org ).

                AUTHOR CONTRIBUTIONS

                S.N. and A.S. carried out the research and wrote the manuscript; B.W.S. and K.M.D. performed site-directed mutagenesis of histones and validation of the generated vectors; W.D.B. performed validation of the transformed yeast library; K.S.-H. and A.S. provided support and advice.

                Article
                nihpa58728
                10.1038/nsmb.1454
                2562305
                18622391
                8a7e77be-d34a-41d8-a2dd-b7703c1784fb
                © 2008 Nature Publishing Group
                History
                Funding
                Funded by: National Institute of General Medical Sciences : NIGMS
                Award ID: R01 GM069905-05 ||GM
                Categories
                Article

                Molecular biology
                Molecular biology

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