Sp6 regulation of Rock1 promoter activity in dental epithelial cells

• Material Type: 博士論文
• Title: Sp6 regulation of Rock1 promoter activity in dental epithelial cells
• Author/Editor: Yanuarysuka, Ryna Dwi; Miyoshi, Keiko; Adiningrat, Arya; Horiguchi, Taigo; Tanimura, Ayako; Hagita, Hiroko; Noma, Takafumi
• Author Heading: Yanuarysuka, Ryna Dwi; Miyoshi, Keiko; Adiningrat, Arya; Horiguchi, Taigo; Tanimura, Ayako; Hagita, Hiroko; Noma, Takafumi
• Publication Date: 2014-08
• Publication Date (W3CDTF): 2014-08
• Alternative Title: 歯原性上皮細胞におけるSp6タンパク質によるRock1遺伝子プロモーター活性の制御; Sp6 regulates Rock1
• Periodical title: The journal of medical investigation : JMI
• No. or year of volume/issue: 61 3-4
• Volume: 61
• Issue: 3-4
• Pages: 306-317
• ISSN (Periodical Title): ISSN : 1343-1420
• Degree grantor/type: 徳島大学
• Date Granted: 2014-09-10
• Dissertation Number: 甲第2756号
• Degree Type: 博士（歯学）
• Text Language Code: eng
• Subject Heading: amelogenesis; dental epithelial cells; Rock1; Sp6; transcription start site
• Target Audience: 一般
• Note (General): Sp6 is a transcription factor of the SP/KLF family and an indispensable regulator of the morphological dynamics of ameloblast differentiation during tooth development. However, the underlying molecular mechanisms remain unclear. We have previously identified one of the Sp6 downstream genes, Rock1, which is involved in ameloblast polarization. In this study, we investigated the transcriptional regulatory mechanisms of Rock1 by Sp6. First, we identified the transcription start sites (TSS) and cloned the 5'- flanking region of Rock1. Serial deletion analyses identified a critical region for Rock1 promoter activity within the 249-bp upstream region of TSS, and chromatin immunoprecipitation assays revealed Sp6-binding to this region. Subsequent transient transfection experiments showed that Rock1 promoter activity is enhanced by Sp6, but reduced by Sp1. Treatment of dental epithelial cells with the GC-selective DNA binding inhibitor, mithramycin A, affected Rock1 promoter activity in loss of enhancement by Sp6, but not repression by Sp1. Further site-directed mutagenesis indicated that the region from -206 to -150 contains responsive elements for Sp6. Taken together, we conclude that Sp6 positively regulates Rock1 transcription by direct binding to the Rock1 promoter region from -206 to -150, which functionally distinct from Sp1.
• Format (IMT): application/pdf
• Access Restrictions: インターネット公開
• Related Material (DOI): 10.2152/jmi.61.306
• Data Provider (Database): 国立情報学研究所 : 学術機関リポジトリデータベース（IRDB）（機関リポジトリ）; https://irdb.nii.ac.jp
• Original Data Provider (Database): 徳島大学 : 徳島大学機関リポジトリ

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