A network of assembly factors is involved in remodeling rRNA elements during preribosome maturation

Author:

Baßler Jochen1,Paternoga Helge1,Holdermann Iris1,Thoms Matthias1,Granneman Sander2,Barrio-Garcia Clara3,Nyarko Afua4,Lee Woonghee55,Stier Gunter1,Clark Sarah A.4,Schraivogel Daniel1,Kallas Martina1,Beckmann Roland3,Tollervey David2,Barbar Elisar4,Sinning Irmi1,Hurt Ed1

Affiliation:

1. Biochemistry Center of Heidelberg University, INF328, D-69120 Heidelberg, Germany

2. Centre for Synthetic and Systems Biology (SynthSys) and Wellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh EH9 3BF, Scotland, UK

3. Gene Center, Department of Chemistry and Biochemistry, University of Munich, 80539 Munich, Germany

4. Department of Biochemistry and Biophysics, Oregon State University, Corvallis, OR 97331

5. National Magnetic Resonance Facility, and Biochemistry Department, University of Wisconsin-Madison, Madison, WI 53706

Abstract

Eukaryotic ribosome biogenesis involves ∼200 assembly factors, but how these contribute to ribosome maturation is poorly understood. Here, we identify a network of factors on the nascent 60S subunit that actively remodels preribosome structure. At its hub is Rsa4, a direct substrate of the force-generating ATPase Rea1. We show that Rsa4 is connected to the central protuberance by binding to Rpl5 and to ribosomal RNA (rRNA) helix 89 of the nascent peptidyl transferase center (PTC) through Nsa2. Importantly, Nsa2 binds to helix 89 before relocation of helix 89 to the PTC. Structure-based mutations of these factors reveal the functional importance of their interactions for ribosome assembly. Thus, Rsa4 is held tightly in the preribosome and can serve as a “distribution box,” transmitting remodeling energy from Rea1 into the developing ribosome. We suggest that a relay-like factor network coupled to a mechano-enzyme is strategically positioned to relocate rRNA elements during ribosome maturation.

Publisher

Rockefeller University Press

Subject

Cell Biology

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