Bartuli Julia, Jungwirth Stefan, Dixit Manisha, Okuda Takumi, Zimmermann Johannes Patrick, Erlacher Matthias, Pan Tao, Volz Asisa, Hüttenhofer Alexander, Warscheid Bettina, Höbartner Claudia, Grimm Clemens, Fischer Utz
Department of Biochemistry 1, Theodor Boveri-Institute, University of Würzburg, Würzburg, Germany.
National Heart Lung and Blood Institute, National Institutes of Health, Bethesda, MD, USA.
Nat Struct Mol Biol. 2025 Sep 4. doi: 10.1038/s41594-025-01653-y.
Transfer RNAs (tRNAs) are widely recognized for their role in translation. Here, we describe a previously unidentified function of tRNA as an assembly chaperone. During poxviral infection, tRNA lacking the anticodon mcmsU34 modification is specifically sequestered from the cellular tRNA pool to promote formation of a multisubunit poxviral RNA polymerase complex (vRNAP). Cryo-electron microscopy analysis of assembly intermediates illustrates how tRNA orchestrates the recruitment of transcription and mRNA processing factors to vRNAP where it controls the transition to the preinitiation complex. This is achieved by an induced fit mechanism that internalizes anticodon base G36 into the anticodon stem, creating a noncanonical tRNA structure and selecting a defined tRNA modification pattern. The role of tRNA as an assembly chaperone extends to the pathogenic Mpox virus, which features a similar vRNAP.
转运RNA(tRNA)因其在翻译过程中的作用而广为人知。在此,我们描述了tRNA作为组装伴侣的一种先前未被识别的功能。在痘病毒感染期间,缺乏反密码子修饰的tRNA会从细胞tRNA池中被特异性隔离,以促进多亚基痘病毒RNA聚合酶复合物(vRNAP)的形成。对组装中间体的冷冻电子显微镜分析表明,tRNA如何协调转录和mRNA加工因子向vRNAP的募集,在vRNAP处它控制向起始前复合物的转变。这是通过一种诱导契合机制实现的,该机制将反密码子碱基G36内化到反密码子茎中,形成一种非经典的tRNA结构并选择特定的tRNA修饰模式。tRNA作为组装伴侣的作用延伸到致病性猴痘病毒,该病毒具有类似的vRNAP。