Literature DB >> 19218532

HistoneHits: a database for histone mutations and their phenotypes.

Hailiang Huang1, Alexandra M Maertens, Edel M Hyland, Junbiao Dai, Anne Norris, Jef D Boeke, Joel S Bader.   

Abstract

Histones are the basic protein components of nucleosomes. They are among the most conserved proteins and are subject to a plethora of post-translational modifications. Specific histone residues are important in establishing chromatin structure, regulating gene expression and silencing, and responding to DNA damage. Here we present HistoneHits, a database of phenotypes for systematic collections of histone mutants. This database combines assay results (phenotypes) with information about sequences, structures, post-translational modifications, and evolutionary conservation. The web interface presents the information through dynamic tables and figures. It calculates the availability of data for specific mutants and for nucleosome surfaces. The database currently includes 42 assays on 677 mutants multiply covering 405 of the 498 residues across yeast histones H3, H4, H2A, and H2B. We also provide an interface with an extensible controlled vocabulary for research groups to submit new data. Preliminary analyses confirm that mutations at highly conserved residues and modifiable residues are more likely to generate phenotypes. Buried residues and residues on the lateral surface tend to generate more phenotypes, while tail residues generate significantly fewer phenotypes than other residues. Yeast mutants are cross referenced with known human histone variants, identifying a position where a yeast mutant causes loss of ribosomal silencing and a human variant increases breast cancer susceptibility. All data sets are freely available for download.

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Year:  2009        PMID: 19218532      PMCID: PMC2666297          DOI: 10.1101/gr.083402.108

Source DB:  PubMed          Journal:  Genome Res        ISSN: 1088-9051            Impact factor:   9.043


  35 in total

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3.  Probing nucleosome function: a highly versatile library of synthetic histone H3 and H4 mutants.

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6.  Epigenetic silencing of RNA polymerase I transcription: a role for DNA methylation and histone modification in nucleolar dominance.

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Review 9.  Histone variants: are they functionally heterogeneous?

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  30 in total

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8.  Combinatorial profiling of chromatin binding modules reveals multisite discrimination.

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Review 9.  High-resolution network biology: connecting sequence with function.

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10.  HHMD: the human histone modification database.

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Journal:  Nucleic Acids Res       Date:  2009-11-05       Impact factor: 16.971

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