File Download

There are no files associated with this item.

  • Find it @ UNIST can give you direct access to the published full text of this article. (UNISTARs only)
Related Researcher

고명곤

Ko, Myunggon
Cancer Epigenetics Lab.
Read More

Views & Downloads

Detailed Information

Cited time in webofscience Cited time in scopus
Metadata Downloads

Full metadata record

DC Field Value Language
dc.citation.endPage 1446 -
dc.citation.number 3 -
dc.citation.startPage 1435 -
dc.citation.title BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS -
dc.citation.volume 338 -
dc.contributor.author Ahn, Jeongeun -
dc.contributor.author Ko, Myung Gon -
dc.contributor.author Lee, Kyuyoung -
dc.contributor.author Oh, Jaehak -
dc.contributor.author Jeon, Sungho -
dc.contributor.author Seong, Rho H -
dc.date.accessioned 2023-12-22T10:10:24Z -
dc.date.available 2023-12-22T10:10:24Z -
dc.date.created 2015-07-24 -
dc.date.issued 2005-12 -
dc.description.abstract SRG3, a mouse homolog of yeast SW13 and human BAF155, is known to be a core component of SWI/SNF chromatin-remodeling complex. We have previously shown that SRG3 plays essential roles in early mouse embryogenesis, brain development, and T-cell development. SRG3 gene expression was differentially regulated depending on the developmental stages and exhibited tissue-specific pattern. In this study, we showed that the functional interactions between Sp and Ets family transcription factors are crucial for the SRG3 expression. Sp I and Sp3 specifically bound to the two canonical Sp-binding sites (GC boxes) at -152 and -114, and a non-canonical Sp-binding site (CCTCCT inotif) at -108 in the SRG3 promoter. Using Drosophila SL2 cells, we found that Various Sp or Ets family members activate the SRG3 promoter through these Sp- or Ets-binding sites, respectively, in a dose-dependent manner. Intriguingly, different combinatorial expression of Ets and Sp factors in SL2 cells resulted in either strong synergistic activation or repression of the SRG3 promoter activity. Moreover, the Sp-mediated activation of SRG3 promoter required the intact Ets-binding element. Taken together, these results Suggest that diverse interactions between Sp1/Sp3 and Ets factors are crucial for the SRG3 gene expression. (c) 2005 Elsevier Inc. All rights reserved. -
dc.identifier.bibliographicCitation BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.338, no.3, pp.1435 - 1446 -
dc.identifier.doi 10.1016/j.bbrc.2005.10.107 -
dc.identifier.issn 0006-291X -
dc.identifier.scopusid 2-s2.0-27744510731 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/12653 -
dc.identifier.url http://www.sciencedirect.com/science/article/pii/S0006291X05023594# -
dc.identifier.wosid 000233710100018 -
dc.language 영어 -
dc.publisher ACADEMIC PRESS INC ELSEVIER SCIENCE -
dc.title Expression of SRG3, a core component of mouse SWI/SNF chromatin-remodeling complex, is regulated by cooperative interactions between Sp1/Sp3 and Ets transcription factors -
dc.type Article -
dc.description.journalRegisteredClass scopus -

qrcode

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.