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Structure and assembly of the Alu domain of the mammalian signal recognition particle

Nature volume 408, pages 167–173 (2000)Cite this article

Abstract

The Alu domain of the mammalian signal recognition particle (SRP) comprises the heterodimer of proteins SRP9 and SRP14 bound to the 5′ and 3′ terminal sequences of SRP RNA. It retards the ribosomal elongation of signal-peptide-containing proteins before their engagement with the translocation machinery in the endoplasmic reticulum. Here we report two crystal structures of the heterodimer SRP9/14 bound either to the 5′ domain or to a construct containing both 5′ and 3′ domains. We present a model of the complete Alu domain that is consistent with extensive biochemical data. SRP9/14 binds strongly to the conserved core of the 5′ domain, which forms a U-turn connecting two helical stacks. Reversible docking of the more weakly bound 3′ domain might be functionally important in the mechanism of translational regulation. The Alu domain structure is probably conserved in other cytoplasmic ribonucleoprotein particles and retroposition intermediates containing SRP9/14-bound RNAs transcribed from Alu repeats or related elements in genomic DNA.

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Figure 1: Mammalian SRP and Alu domain RNA constructs.
Figure 2: Structure of the Alu RNA 5′ domain (SA50).
Figure 3: Protein recognition of the conserved fold of the Alu RNA τ-junction.
Figure 4: Stereo image of experimental electron density for SA88 RNA.
Figure 5: Structure of the Alu domain of the mammalian SRP (see Fig. 1 for colours).

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Acknowledgements

O.W. received a pre-doctoral fellowship from the Boehringer-Ingelheim-Fonds. K.S. is supported by a START subsidy and a grant from the Swiss National Science Foundation and the Canton de Genève. K.S. and S.C. are both principal investigators belonging to SRPNET, a research network of the European Union Training and Mobility in Research program, which also supported K.W. We thank members of the EMBL/ESRF Joint Structural Biology Group (JSBG) and the staff of BM30 and ID13 for support on ESRF beamlines; in particular, A. Thompson for the europium MAD experiment and A. Perrakis for the ID13 measurements and help with wARP. C. Petosa commented critically on the manuscript.

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  1. European Molecular Laboratory Biology, Grenoble Outstation, BP 156X, Grenoble, F-38042 Cedex 9, France

    Oliver Weichenrieder, Klemens Wild & Stephen Cusack

  2. Département de Biologie Cellulaire Université de Genève, Sciences III, Geneva, CH-1211 4, Switzerland

    Katharina Strub

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Correspondence to Stephen Cusack.

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Weichenrieder, O., Wild, K., Strub, K. et al. Structure and assembly of the Alu domain of the mammalian signal recognition particle. Nature 408, 167–173 (2000). https://doi.org/10.1038/35041507

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