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ID 32850
JaLCDOI
フルテキストURL
fulltext.pdf 2.18 MB
著者
Wu, Yun-Feng Department of Matrix Medicine, Faculty of Medicine, Oita University
Matsuo, Noritaka Department of Matrix Medicine, Faculty of Medicine, Oita University
Sumiyoshi, Hideaki Department of Matrix Medicine, Faculty of Medicine, Oita University
Yoshioka, Hidekatsu Department of Matrix Medicine, Faculty of Medicine, Oita University
抄録

The purpose of this study was to clarify the mechanism responsible for the transcriptional regulation of the mouse Col5a3 gene in osteoblastic cells. Transient transfection into rat osteosarcoma ROS17/2.8 cells demonstrated that a region from nucleotides 337 to 1 was involved in the transcriptional activity of the Col5a3 gene. An electrophoretic mobility shift assay showed that Sp1/Sp3 and CBF/NF-Y bound to a GC-rich domain (194/186) and a CCAAT box (134/130) in the Col5a3 gene, respectively. Introduction of mutations or deletion into a GC-rich domain, the CCAAT box, or both elements decreased the transcription activity. Overexpression of Sp1 increases the transcription activity and interferes with Sp family binding to the GC-rich domain to decrease promoter activity. Therefore, the transcription of the mouse Col5a3 gene is cooperatively regulated by Sp1 and CBF/NF-Y in osteoblastic cells.

キーワード
type V collagen
Sp1
CBF/NF-Y
gene regulation
osteoblastic cell
Amo Type
Original Article
出版物タイトル
Acta Medica Okayama
発行日
2010-04
64巻
2号
出版者
Okayama University Medical School
開始ページ
95
終了ページ
108
ISSN
0386-300X
NCID
AA00508441
資料タイプ
学術雑誌論文
言語
英語
論文のバージョン
publisher
査読
有り
PubMed ID
Web of Science KeyUT