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AKT1 is positively regulated by G-quadruplexes in its promoter and 3'-UTR.
Zhang, Lanlan; Yan, Ting; Wang, Wenmeng; Wu, Qiong; Li, Guangyue; Li, Dangdang; Stovall, Daniel B; Wang, Yunxuan; Li, Yuhua; Sui, Guangchao.
Afiliação
  • Zhang L; Key Laboratory of Saline-alkali Vegetation Ecology Restoration, Ministry of Education, College of Life Science, Northeast Forestry University, Harbin, 150040, China.
  • Yan T; Key Laboratory of Saline-alkali Vegetation Ecology Restoration, Ministry of Education, College of Life Science, Northeast Forestry University, Harbin, 150040, China.
  • Wang W; Key Laboratory of Saline-alkali Vegetation Ecology Restoration, Ministry of Education, College of Life Science, Northeast Forestry University, Harbin, 150040, China.
  • Wu Q; Key Laboratory of Saline-alkali Vegetation Ecology Restoration, Ministry of Education, College of Life Science, Northeast Forestry University, Harbin, 150040, China.
  • Li G; Key Laboratory of Saline-alkali Vegetation Ecology Restoration, Ministry of Education, College of Life Science, Northeast Forestry University, Harbin, 150040, China.
  • Li D; Key Laboratory of Saline-alkali Vegetation Ecology Restoration, Ministry of Education, College of Life Science, Northeast Forestry University, Harbin, 150040, China.
  • Stovall DB; College of Arts and Sciences, Winthrop University, Rock Hill, SC, 29733, United States.
  • Wang Y; Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, 150081, China.
  • Li Y; Key Laboratory of Saline-alkali Vegetation Ecology Restoration, Ministry of Education, College of Life Science, Northeast Forestry University, Harbin, 150040, China. Electronic address: lyhshen@nefu.edu.cn.
  • Sui G; Key Laboratory of Saline-alkali Vegetation Ecology Restoration, Ministry of Education, College of Life Science, Northeast Forestry University, Harbin, 150040, China. Electronic address: gcsui@nefu.edu.cn.
Biochem Biophys Res Commun ; 561: 93-100, 2021 07 05.
Article em En | MEDLINE | ID: mdl-34020144
AKT1 plays a key role in cell growth and survival, and its activation in cancers is mediated by different mechanisms. In this study, we investigated the potential of G-quadruplex (G4) formation by multiple consecutive G-tracts in the AKT1 promoter and its 3'-UTR. In circular dichroism analyses, synthetic oligonucleotides based on these G-tract regions showed molar ellipticity peaks at specific wavelengths of G4 structures. We verified G4 forming potential of these oligonucleotides using dimethyl sulfate footprinting, gel-shift and immunostaining assays. In reporter assays, mutations of the G-tracts in either the promoter or the 3'-UTR of AKT1 reduced expression mediated by these G-rich regions, suggesting positive regulation of AKT1 gene expression by these G4 structures. Furthermore, SP1 bound to its consensus sites regardless of the presence of G4 motifs in the AKT1 promoter, and both the G4 motifs and SP1 binding sites were needed to reach the strongest promoter strength.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Proto-Oncogênicas c-akt / Quadruplex G / Neoplasias Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Proto-Oncogênicas c-akt / Quadruplex G / Neoplasias Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article