An accurately preorganized IRES RNA structure enables eIF4G capture for initiation of viral translation

作者：Imai Shunsuke; Kumar Parimal; Hellen Christopher U T; D'Souza Victoria M^*; Wagner Gerhard^*

来源：Nature Structural & Molecular Biology, 2016, 23(9): 859-864.

DOI：10.1038/nsmb.3280

Many viruses bypass canonical cap-dependent translation in host cells by using internal ribosomal entry sites (IRESs) in their transcripts; IRESs hijack initiation factors for the assembly of initiation complexes. However, it is currently unknown how 1RES RNAs recognize initiation factors that have no endogenous RNA binding partners; in a prominent example, the IRES of encephalomyocarditis virus (EMCV) interacts with the HEAT-1 domain of eukaryotic initiation factor 4G (eIF4G). Here we report the solution structure of the J-K region of this 1RES and show that its stems are precisely organized to position protein-recognition bulges. This multisite interaction mechanism operates on an all-or-nothing principle in which all domains are required. This preorganization is accomplished by an 'adjuster module': a pentaloop motif that acts as a dual-sided docking station for base pair receptors. Because subtle changes in the orientation abrogate protein capture, our study highlights how a viral RNA acquires affinity for a target protein.

• 出版日期2016-9