Expression Génétique Microbienne, Université de Paris Cité & CNRS, IBPC, 13 Rue Pierre et Marie Curie, 75005 Paris, France.
Institut de Biologie Physico-Chimique, Paris Sciences et Lettres University, CNRS UMR8261, EGM, 75005 Paris, France.
Genes (Basel). 2023 Jul 31;14(8):1566. doi: 10.3390/genes14081566.
DEAD-box RNA helicases are ATP-dependent RNA binding proteins and RNA-dependent ATPases that possess weak, nonprocessive unwinding activity in vitro, but they can form long-lived complexes on RNAs when the ATPase activity is inhibited. Ded1 is a yeast DEAD-box protein, the functional ortholog of mammalian DDX3, that is considered important for the scanning efficiency of the 48S pre-initiation complex ribosomes to the AUG start codon. We used a modified PAR-CLIP technique, which we call quicktime PAR-CLIP (qtPAR-CLIP), to crosslink Ded1 to 4-thiouridine-incorporated RNAs in vivo using UV light centered at 365 nm. The irradiation conditions are largely benign to the yeast cells and to Ded1, and we are able to obtain a high efficiency of crosslinking under physiological conditions. We find that Ded1 forms crosslinks on the open reading frames of many different mRNAs, but it forms the most extensive interactions on relatively few mRNAs, and particularly on mRNAs encoding certain ribosomal proteins and translation factors. Under glucose-depletion conditions, the crosslinking pattern shifts to mRNAs encoding metabolic and stress-related proteins, which reflects the altered translation. These data are consistent with Ded1 functioning in the regulation of translation elongation, perhaps by pausing or stabilizing the ribosomes through its ATP-dependent binding.
DEAD-box RNA 解旋酶是一种依赖于 ATP 的 RNA 结合蛋白和 RNA 依赖性 ATP 酶,在体外具有较弱的、非连续的解旋活性,但当 ATP 酶活性被抑制时,它们可以在 RNA 上形成长寿命的复合物。Ded1 是一种酵母 DEAD-box 蛋白,是哺乳动物 DDX3 的功能同源物,被认为对 48S 起始前复合物核糖体到 AUG 起始密码子的扫描效率很重要。我们使用了一种改良的 PAR-CLIP 技术,我们称之为快速 PAR-CLIP(qtPAR-CLIP),使用波长为 365nm 的紫外线将 4-硫代尿嘧啶掺入的 RNA 与体内的 Ded1 交联。辐照条件对酵母细胞和 Ded1 基本无害,我们能够在生理条件下获得很高的交联效率。我们发现 Ded1 在许多不同的 mRNA 的开放阅读框上形成交联,但它在相对较少的 mRNA 上形成最广泛的相互作用,特别是在编码某些核糖体蛋白和翻译因子的 mRNA 上。在葡萄糖耗尽条件下,交联模式转移到编码代谢和应激相关蛋白的 mRNA 上,这反映了翻译的改变。这些数据与 Ded1 在翻译延伸的调节中发挥作用的观点一致,可能通过其依赖于 ATP 的结合使核糖体暂停或稳定。