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DDX3 regulates cell growth through translational control of cyclin E1

  • Ming Chih Lai
  • , Wen Cheng Chang
  • , Sheau Yann Shieh
  • , Woan Yuh Tarn*
  • *此作品的通信作者
  • Academia Sinica - Institute of Biomedical Sciences
  • National Cheng Kung University

研究成果: 期刊稿件文章同行評審

160 引文 斯高帕斯(Scopus)

摘要

DDX3 belongs to the DEAD box family of RNA helicases, but the details of its biological function remain largely unclear. Here we show that knockdown of DDX3 expression impedes G1/S-phase transition of the cell cycle. To know how DDX3 may act in cell cycle control, we screened for cellular mRNA targets of DDX3. Many of the identified DDX3 targets encoded cell cycle regulators, including G1/S-specific cyclin E1. DDX3 depletion specifically downregulates translation of cyclin E1 mRNA. Moreover, our data suggest that DDX3 participates in translation initiation of targeted mRNAs as well as in cell growth control via its RNA helicase activity. Consistent with these findings, we show that in the temperature-sensitive DDX3 mutant hamster cell line tsET24, cyclin E1 expression is downregulated at a nonpermissive temperature that inactivates mutant DDX3. Taken together, our results indicate that DDX3 is critical for translation of cyclin E1 mRNA, which provides an alternative mechanism for regulating cyclin E1 expression during the cell cycle.

原文英語
頁(從 - 到)5444-5453
頁數10
期刊Molecular and Cellular Biology
30
發行號22
DOIs
出版狀態已出版 - 11 2010
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