Insertion of the Biogenesis Factor Rei1 Probes the Ribosomal Tunnel during 60S Maturation

被引:78
作者
Greber, Basil Johannes [1 ]
Gerhardy, Stefan [2 ]
Leitner, Alexander [3 ]
Leibundgut, Marc [1 ]
Salem, Michele [4 ]
Boehringer, Daniel [1 ]
Leulliot, Nicolas [4 ]
Aebersold, Ruedi [3 ,5 ]
Panse, Vikram Govind
Ban, Nenad [1 ]
机构
[1] ETH, Dept Biol, Inst Mol Biol & Biophys, CH-8093 Zurich, Switzerland
[2] ETH, Dept Biol, Inst Biochem, CH-8093 Zurich, Switzerland
[3] ETH, Dept Biol, Inst Mol Syst Biol, CH-8093 Zurich, Switzerland
[4] Univ Paris 05, Sorbonne Paris Cite, CNRS, UMR 8015,Lab Cristallog & RMN Biol,Fac Pharm, F-75006 Paris, France
[5] Univ Zurich, Fac Sci, CH-8057 Zurich, Switzerland
基金
欧洲研究理事会; 瑞士国家科学基金会;
关键词
EM STRUCTURE DETERMINATION; NUCLEAR EXPORT RECEPTOR; CRYO-EM; SACCHAROMYCES-CEREVISIAE; EUKARYOTIC RIBOSOME; CRYSTAL-STRUCTURE; PRERIBOSOMAL FACTORS; DIAMOND-SYNDROME; BUDDING YEAST; PRE-RIBOSOMES;
D O I
10.1016/j.cell.2015.11.027
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Eukaryotic ribosome biogenesis depends on several hundred assembly factors to produce functional 40S and 60S ribosomal subunits. The final phase of 60S subunit biogenesis is cytoplasmic maturation, which includes the proofreading of functional centers of the 60S subunit and the release of several ribosome biogenesis factors. We report the cryo-electron microscopy (cryo-EM) structure of the yeast 60S subunit in complex with the biogenesis factors Rei1, Arx1, and Alb1 at 3.4 angstrom resolution. In addition to the network of interactions formed by Alb1, the structure reveals a mechanism for ensuring the integrity of the ribosomal polypeptide exit tunnel. Arx1 probes the entire set of inner-ring proteins surrounding the tunnel exit, and the C terminus of Rei1 is deeply inserted into the ribosomal tunnel, where it forms specific contacts along almost its entire length. We provide genetic and biochemical evidence that failure to insert the C terminus of Rei1 precludes subsequent steps of 60S maturation.
引用
收藏
页码:91 / 102
页数:12
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