Mechanism of 5S RNP recruitment and helicase‐surveilled rRNA maturation during pre‐60S biogenesis

Author:

Lau Benjamin1ORCID,Huang Zixuan2ORCID,Kellner Nikola1,Niu Shuangshuang3,Berninghausen Otto3,Beckmann Roland3ORCID,Hurt Ed1ORCID,Cheng Jingdong2ORCID

Affiliation:

1. Heidelberg University Biochemistry Center (BZH) Heidelberg Germany

2. Minhang Hospital & Institutes of Biomedical Sciences, Shanghai Key Laboratory of Medical Epigenetics, International Co‐laboratory of Medical Epigenetics and Metabolism Fudan University Shanghai China

3. Gene Center Ludwig‐Maximilians‐Universität München Munich Germany

Abstract

AbstractRibosome biogenesis proceeds along a multifaceted pathway from the nucleolus to the cytoplasm that is extensively coupled to several quality control mechanisms. However, the mode by which 5S ribosomal RNA is incorporated into the developing pre‐60S ribosome, which in humans links ribosome biogenesis to cell proliferation by surveillance by factors such as p53–MDM2, is poorly understood. Here, we report nine nucleolar pre‐60S cryo‐EM structures from Chaetomium thermophilum, one of which clarifies the mechanism of 5S RNP incorporation into the early pre‐60S. Successive assembly states then represent how helicases Dbp10 and Spb4, and the Pumilio domain factor Puf6 act in series to surveil the gradual folding of the nearby 25S rRNA domain IV. Finally, the methyltransferase Spb1 methylates a universally conserved guanine nucleotide in the A‐loop of the peptidyl transferase center, thereby licensing further maturation. Our findings provide insight into the hierarchical action of helicases in safeguarding rRNA tertiary structure folding and coupling to surveillance mechanisms that culminate in local RNA modification.

Funder

Science and Technology Commission of Shanghai Municipality

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Biochemistry

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