201. Tet1 is required for Rb phosphorylation during G1/S phase transition
- Author
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Yanru Wang, Qimin Zhang, Denglong Wu, Xin Zhao, Yiqin Wang, Xuemei Chen, Qing Xu, Ziqi Zhu, Yi Yu, Longxia Xu, and Shengsong Huang
- Subjects
Transcription, Genetic ,Cyclin A ,Blotting, Western ,Biophysics ,Biology ,Transfection ,Biochemistry ,Retinoblastoma Protein ,S Phase ,Mice ,Cyclin D1 ,Proto-Oncogene Proteins ,Animals ,Humans ,Phosphorylation ,RNA, Small Interfering ,Molecular Biology ,Cell Proliferation ,Regulation of gene expression ,Cell growth ,Lentivirus ,G1 Phase ,Cell Biology ,Molecular biology ,Chromatin ,Cell biology ,DNA-Binding Proteins ,DNA demethylation ,HEK293 Cells ,Gene Expression Regulation ,Gene Knockdown Techniques ,DNA methylation ,biology.protein ,NIH 3T3 Cells - Abstract
DNA methylation plays an important role in many biological processes, including regulation of gene expression, maintenance of chromatin conformation and genomic stability. TET-family proteins convert 5-methylcytosine (5mC) to 5-hydroxymethylcytosine (5hmC), which indicates that these enzymes may participate in DNA demethylation. The function of TET1 has not yet been well characterized in somatic cells. Here, we show that depletion of Tet1 in NIH3T3 cells inhibits cell growth. Furthermore, Tet1 knockdown blocks cyclin D1 accumulation in G1 phase, inhibits Rb phosphorylation and consequently delays entrance to G1/S phase. Taken together, this study demonstrates that Tet1 is required for cell proliferation and that this process is mediated through the Rb pathway.
- Published
- 2013