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dc.contributor.authorHan, Leen
dc.contributor.authorPandian, Ganesh N.en
dc.contributor.authorChandran, Anandhakumaren
dc.contributor.authorSato, Shinsukeen
dc.contributor.authorTaniguchi, Junichien
dc.contributor.authorKashiwazaki, Gengoen
dc.contributor.authorSawatani, Yoshitoen
dc.contributor.authorHashiya, Kaorien
dc.contributor.authorBando, Toshikazuen
dc.contributor.authorXu, Yufangen
dc.contributor.authorQian, Xuhongen
dc.contributor.authorSugiyama, Hiroshien
dc.contributor.alternative佐藤, 慎祐ja
dc.contributor.alternative橋谷, かおりja
dc.contributor.alternative板東, 俊和ja
dc.contributor.alternative杉山, 弘ja
dc.date.accessioned2018-04-25T05:33:28Z-
dc.date.available2018-04-25T05:33:28Z-
dc.date.issued2015-07-20-
dc.identifier.issn1521-3773-
dc.identifier.urihttp://hdl.handle.net/2433/230861-
dc.description.abstractSynthetic dual‐function ligands targeting specific DNA sequences and histone‐modifying enzymes were applied to achieve regulatory control over multi‐gene networks in living cells. Unlike the broad array of targeting small molecules for histone deacetylases (HDACs), few modulators are known for histone acetyltransferases (HATs), which play a central role in transcriptional control. As a novel chemical approach to induce selective HAT‐regulated genes, we conjugated a DNA‐binding domain (DBD) “I” to N‐(4‐chloro‐3‐trifluoromethyl‐phenyl)‐2‐ethoxy‐benzamide (CTB), an artificial HAT activator. In vitro enzyme activity assays and microarray studies were used to demonstrate that distinct functional small molecules could be transformed to have identical bioactivity when conjugated with a targeting DBD. This proof‐of‐concept synthetic strategy validates the switchable functions of HDACs and HATs in gene regulation and provides a molecular basis for developing versatile bioactive ligands.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherWiley-VCH Verlagen
dc.rightsThis is the accepted version of the following article: [Angewandte Chemie International Edition, (2015) 54, 30, 8700-8703] , which has been published in final form at https://doi.org/10.1002/anie.201503607. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.en
dc.rightsThe full-text file will be made open to the public on 15 July 2016 in accordance with publisher's 'Terms and Conditions for Self-Archiving'.en
dc.rightsThis is not the published version. Please cite only the published version.en
dc.rightsこの論文は出版社版でありません。引用の際には出版社版をご確認ご利用ください。ja
dc.subjectDNA recognitionen
dc.subjectepigeneticsen
dc.subjectgene expressionen
dc.subjecthistone modificationen
dc.subjectsynthetic biologen
dc.titleA Synthetic DNA-Binding Domain Guides Distinct Chromatin-Modifying Small Molecules to Activate an Identical Gene Networken
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleAngewandte Chemie International Editionen
dc.identifier.volume54-
dc.identifier.issue30-
dc.identifier.spage8700-
dc.identifier.epage8703-
dc.relation.doi10.1002/anie.201503607-
dc.textversionauthor-
dc.identifier.pmid26094767-
dcterms.accessRightsopen access-
datacite.date.available2016-07-15-
datacite.awardNumber24225005-
datacite.awardNumber24310155-
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
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