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Rrp15 affects cell cycle, proliferation, and apoptosis in NIH3T3 cells.
Wu, Tao; Ren, Mei-Xia; Chen, Guo-Ping; Jin, Zheng-Ming; Wang, Gang.
Afiliação
  • Wu T; Department of Cardiology The First Affiliated Hospital School of Medicine Zhejiang University Hangzhou China.
  • Ren MX; Department of Cardiology The First Affiliated Hospital School of Medicine Zhejiang University Hangzhou China.
  • Chen GP; Department of Endocrinology The First Affiliated Hospital School of Medicine Zhejiang University Hangzhou China.
  • Jin ZM; Department of Cardiology The First Affiliated Hospital School of Medicine Zhejiang University Hangzhou China.
  • Wang G; Cancer Institute of Integrative Medicine Tongde Hospital of Zhejiang Province Zhejiang Provincial Academy of Traditional Chinese Medicine Hangzhou China.
FEBS Open Bio ; 6(11): 1085-1092, 2016 Nov.
Article em En | MEDLINE | ID: mdl-27833849
Riken 2810430M08 (hereinafter referred to as Rrp15) is a newly identified and reported gene from the mouse genome. In our previous work, we found that the gene had a relationship with the proliferation and activation of T cells. Rrp15 protein is highly homologous with RRP15 (budding yeast), which has an important role in ribosomal RNA processing. We explored the potential function of Rrp15 in apoptosis, cell proliferation, and its involvement with RNA in the nucleus. We constructed a knockdown of the Rrp15 gene in NIH3T3 cells and then performed real-time PCR, western blotting, flow cytometry, and immunofluorescence to determine the function of the Rrp15 gene. Knockdown of the Rrp15 gene suppresses proliferation and induces apoptosis. We also found that the Rrp15 protein was normally distributed in the nucleus and bound to RNA or pre-RNA in the nucleus. Additionally, Rrp15 altered the activity of the 20S proteasome. Rrp15 promotes proliferation and inhibits apoptosis in NIH3T3 cells and may have a relationship with RNA in the nucleus.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article