| pubmed-article:18493056 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:18493056 | lifeskim:mentions | umls-concept:C0205245 | lld:lifeskim |
| pubmed-article:18493056 | lifeskim:mentions | umls-concept:C0013138 | lld:lifeskim |
| pubmed-article:18493056 | lifeskim:mentions | umls-concept:C0062776 | lld:lifeskim |
| pubmed-article:18493056 | lifeskim:mentions | umls-concept:C1880022 | lld:lifeskim |
| pubmed-article:18493056 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:18493056 | pubmed:dateCreated | 2008-5-21 | lld:pubmed |
| pubmed-article:18493056 | pubmed:abstractText | Di- and trimethylation of histone H4 lysine20 (H4K20) are thought to play an important role in controlling gene expression in vertebrates and in Drosophila. By inducing a null mutation in Drosophila Suv4-20, we show that it encodes the histone H4 lysine20 di- and trimethyltransferase. In Suv4-20 mutants, the H4K20 di- and trimethyl marks are strongly reduced or absent, and the monomethyl mark is significantly increased. We find that even with this biochemical function, Suv4-20 is not required for survival and does not control position-effect variegation (PEV). | lld:pubmed |
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| pubmed-article:18493056 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:18493056 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:18493056 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:18493056 | pubmed:month | May | lld:pubmed |
| pubmed-article:18493056 | pubmed:issn | 0016-6731 | lld:pubmed |
| pubmed-article:18493056 | pubmed:author | pubmed-author:StewardRuthR | lld:pubmed |
| pubmed-article:18493056 | pubmed:author | pubmed-author:SakaguchiAyak... | lld:pubmed |
| pubmed-article:18493056 | pubmed:author | pubmed-author:KarachentsevD... | lld:pubmed |
| pubmed-article:18493056 | pubmed:author | pubmed-author:DruzhininaMar... | lld:pubmed |
| pubmed-article:18493056 | pubmed:author | pubmed-author:Seth-Pasricha... | lld:pubmed |
| pubmed-article:18493056 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:18493056 | pubmed:volume | 179 | lld:pubmed |
| pubmed-article:18493056 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:18493056 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:18493056 | pubmed:pagination | 317-22 | lld:pubmed |
| pubmed-article:18493056 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:18493056 | pubmed:year | 2008 | lld:pubmed |
| pubmed-article:18493056 | pubmed:articleTitle | Functional characterization of the Drosophila Hmt4-20/Suv4-20 histone methyltransferase. | lld:pubmed |
| pubmed-article:18493056 | pubmed:affiliation | Department of Molecular Biology and Biochemistry, Waksman Institute, New Jersey Cancer Center, Rutgers University, Piscataway, NJ 08854-8020, USA. | lld:pubmed |
| pubmed-article:18493056 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:18493056 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:18493056 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:18493056 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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