HistoneHits: A database for histone mutations and their phenotypes
- Hailiang Huang1,2,
- Alexandra M. Maertens2,3,
- Edel M. Hyland2,4,
- Junbiao Dai2,4,
- Anne Norris2,4,
- Jef D. Boeke2,4 and
- Joel S. Bader1,2,5
- 1Department of Biomedical Engineering, Johns Hopkins University and School of Medicine, Baltimore, Maryland 21218, USA;
- 2High Throughput Biology Center, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA;
- 3Department of Environmental Health Sciences, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland 21205, USA;
- 4Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA
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 (http://histonehits.org), 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.
Footnotes
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↵5 Corresponding author.
↵E-mail joel.bader{at}jhu.edu; fax (410) 516-5294.
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[Supplemental material is available online at www.genome.org.]
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Article is online at http://www.genome.org/cgi/doi/10.1101/gr.083402.108.
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- Received July 18, 2008.
- Accepted December 30, 2008.
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Freely available online through the open access option.
- Copyright © 2009 by Cold Spring Harbor Laboratory Press











