Direct atomic force microscopy visualization of integration host factor-induced DNA bending structure of the promoter regulatory region on the Pseudomonas TOL plasmid
DC Field | Value | Language |
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dc.contributor.author | Seong, GiHun | - |
dc.contributor.author | Kobatake, Eiry | - |
dc.contributor.author | Aizawa, Masuo | - |
dc.contributor.author | Miura, Koshiro | - |
dc.contributor.author | Nakazawa, Atsushi | - |
dc.date.accessioned | 2021-06-24T01:03:18Z | - |
dc.date.available | 2021-06-24T01:03:18Z | - |
dc.date.issued | 2002-02 | - |
dc.identifier.issn | 0006-291X | - |
dc.identifier.issn | 1090-2104 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/46831 | - |
dc.description.abstract | Atomic force microscopy (AFM) was used to analyze DNA bending induced by integration host factor (IHF). The direct AFM visualization of IHF-DNA complexes on the OP1 promoter regulatory regions on the Pseudomonas TOL plasmid showed that there was no intrinsic DNA bend in the OP1 promoter region, but a sharp DNA bend was induced by binding of IHF to the region between the upstream regulatory sequence and the promoter sequence. The DNA bending angles were distributed with a mean bend angle of 123degrees The IHF-DNA complexes were shown to bend at the IHF binding site giving rise to an asymmetric structure. These results provide direct evidence that IHF is required functionally for activation of OP1 transcription and support the DNA-loop model that the sharp DNA bend induced by binding of IHF facilitates the contact between RNA polymerase bound by the promoter sequence and XyIR protein attached to the upstream sequence in the OP1 promoter. (C) 2002 Elsevier Science (USA). | - |
dc.format.extent | 6 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | ACADEMIC PRESS INC ELSEVIER SCIENCE | - |
dc.title | Direct atomic force microscopy visualization of integration host factor-induced DNA bending structure of the promoter regulatory region on the Pseudomonas TOL plasmid | - |
dc.type | Article | - |
dc.publisher.location | 미국 | - |
dc.identifier.doi | 10.1006/bbrc.2002.6443 | - |
dc.identifier.scopusid | 2-s2.0-0036293872 | - |
dc.identifier.wosid | 000173990800025 | - |
dc.identifier.bibliographicCitation | BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.291, no.2, pp 361 - 366 | - |
dc.citation.title | BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS | - |
dc.citation.volume | 291 | - |
dc.citation.number | 2 | - |
dc.citation.startPage | 361 | - |
dc.citation.endPage | 366 | - |
dc.type.docType | Article | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
dc.relation.journalResearchArea | Biophysics | - |
dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
dc.relation.journalWebOfScienceCategory | Biophysics | - |
dc.subject.keywordPlus | ESCHERICHIA-COLI | - |
dc.subject.keywordPlus | BINDING-SITES | - |
dc.subject.keywordPlus | PROTEIN | - |
dc.subject.keywordPlus | COMPLEXES | - |
dc.subject.keywordPlus | GENE | - |
dc.subject.keywordPlus | IHF | - |
dc.subject.keywordPlus | RECOMBINATION | - |
dc.subject.keywordAuthor | atomic force microscopy | - |
dc.subject.keywordAuthor | DNA bending | - |
dc.subject.keywordAuthor | IHF protein | - |
dc.subject.keywordAuthor | protein-DNA complexes | - |
dc.subject.keywordAuthor | TOL plasmid | - |
dc.identifier.url | https://www.sciencedirect.com/science/article/pii/S0006291X02964430?via%3Dihub | - |
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