Zhang Yandong, You Jin, Wang Xingshun, Weber Jason
Department of Biology, South University of Science and Technology of China, Shenzhen, Guangdong, People's Republic of China
Department of Biology, South University of Science and Technology of China, Shenzhen, Guangdong, People's Republic of China.
Mol Cell Biol. 2015 Sep 1;35(17):2918-31. doi: 10.1128/MCB.00315-15. Epub 2015 Jun 22.
DEAD/DEAH box RNA helicases play essential roles in numerous RNA metabolic processes, such as mRNA translation, pre-mRNA splicing, ribosome biogenesis, and double-stranded RNA sensing. Herein we show that a recently characterized DEAD/DEAH box RNA helicase, DHX33, promotes mRNA translation initiation. We isolated intact DHX33 protein/RNA complexes in cells and identified several ribosomal proteins, translation factors, and mRNAs. Reduction of DHX33 protein levels markedly reduced polyribosome formation and caused the global inhibition of mRNA translation that was rescued with wild-type DHX33 but not helicase-defective DHX33. Moreover, we observed an accumulation of mRNA complexes with the 80S ribosome in the absence of functional DHX33, consistent with a stalling in initiation, and DHX33 more preferentially promoted structured mRNA translation. We conclude that DHX33 functions to promote elongation-competent 80S ribosome assembly at the late stage of mRNA translation initiation. Our results reveal a newly recognized function of DHX33 in mRNA translation initiation, further solidifying its central role in promoting cell growth and proliferation.
DEAD/DEAH盒RNA解旋酶在众多RNA代谢过程中发挥着重要作用,如mRNA翻译、前体mRNA剪接、核糖体生物合成以及双链RNA传感。在此我们表明,一种最近被鉴定的DEAD/DEAH盒RNA解旋酶DHX33可促进mRNA翻译起始。我们在细胞中分离出完整的DHX33蛋白/RNA复合物,并鉴定出几种核糖体蛋白、翻译因子和mRNA。DHX33蛋白水平的降低显著减少了多核糖体的形成,并导致mRNA翻译的整体抑制,野生型DHX33可挽救这种抑制,但解旋酶缺陷型DHX33则不能。此外,我们观察到在缺乏功能性DHX33的情况下,mRNA与80S核糖体的复合物会积累,这与起始过程中的停滞一致,并且DHX33更优先促进结构化mRNA的翻译。我们得出结论,DHX33在mRNA翻译起始后期发挥作用,促进具有延伸能力的80S核糖体组装。我们的结果揭示了DHX33在mRNA翻译起始中一种新认识的功能,进一步巩固了其在促进细胞生长和增殖中的核心作用。