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bioRxiv · 10.1101/2022.02.24.481786

Sequence-directed RNA remodeling within a topologically complex RNP substrate

Cruz Ruiz, V.·Sekulski, K.·Peddada, N.·Sailer, C.·Balasubramanian, S.·Weirich, C.·Stengel, F.·Erzberger, J. P.
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Abstract

DEAD-box ATPases are ubiquitous enzymes essential in all aspects of RNA biology. However, the limited in vitro catalytic activities described for these enzymes is at odds with their complex cellular roles, most notably in driving large-scale RNA remodeling steps during the assembly of ribonucleoproteins (RNPs). We describe cryo-EM structures of 60S ribosomal biogenesis intermediates that reveal how context-specific RNA unwinding by the DEAD-box ATPase Spb4 results in extensive, sequence-directed remodeling of rRNA secondary structure. Multiple cis and trans interactions stabilize a post-catalytic, high-energy intermediate that drives the organization of the root helix structure within rRNA domain IV. This mechanism explains how limited strand separation by DEAD-box ATPases is leveraged to provide non-equilibrium directionality and ensure efficient and accurate RNP assembly.

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Cruz Ruiz, V., Sekulski, K., Peddada, N., Sailer, C., Balasubramanian, S., Weirich, C., Stengel, F., Erzberger, J. P.. 2022-02-24. Sequence-directed RNA remodeling within a topologically complex RNP substrate. https://doi.org/10.1101/2022.02.24.481786

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