Ribonucleotide reductase small subunit p53R2 facilitates p21 induction of G1 arrest under UV irradiation

Lijun Xue, Bingsen Zhou, Xiyong Liu, Yvonne Heung, Jennifer Chau, Emilie Chu, Shan Li, Chunglin Jiang, Frank Un, Yun Yen

研究成果: 雜誌貢獻文章同行評審

39 引文 斯高帕斯(Scopus)


p53R2, which is one of the two known ribonucleotide reductase small subunits (the other being M2), is suggested to play an important role in supplying deoxynucleotide triphosphates (dNTP) for DNA repair during the G 1 or G2 phase of the cell cycle. The ability of p53R2 to supply dNTPs for repairing DNA damages requires the presence of a functional p53 tumor suppressor. Here, we report in vivo physical interaction and colocalization of p53R2 and p21 before DNA damage. Mammalian two-hybrid assay further indicates that the amino acids 1 to 113 of p53R2 are critical for interacting with the NH2-terminal region (amino acids 1-93) of p21. The binding between p21 and p53R2 decreases inside the nucleus in response to UV, the time point of which corresponds to the increased binding of p21 with cyclin-dependent kinase-2 (Cdk2), and the decreased Cdk2 activity in the nucleus at G1. Interestingly, p53R2 dissociates from p21 but facilitates the accumulation of p21 in the nucleus in response to UV. On the other hand, the ribonucleotide reductase activity increases at the corresponding time in response to UV. These data suggest a new function of p53R2 of cooperating with p21 during DNA repair at G1 arrest.

頁(從 - 到)16-21
期刊Cancer Research
出版狀態已發佈 - 1月 1 2007

ASJC Scopus subject areas

  • 腫瘤科
  • 癌症研究


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