Literature DB >> 26582754

Protein localisation by electron microscopy reveals the architecture of the yeast spliceosomal B complex.

Norbert Rigo1, Chengfu Sun1, Patrizia Fabrizio1, Berthold Kastner2, Reinhard Lührmann2.   

Abstract

The spliceosome assembles on a pre-mRNA intron by binding of five snRNPs and numerous proteins, leading to the formation of the pre-catalytic B complex. While the general morphology of the B complex is known, the spatial arrangement of proteins and snRNP subunits within it remain to be elucidated. To shed light on the architecture of the yeast B complex, we immuno-labelled selected proteins and located them by negative-stain electron microscopy. The B complex exhibited a triangular shape with main body, head and neck domains. We located the U5 snRNP components Brr2 at the top and Prp8 and Snu114 in the centre of the main body. We found several U2 SF3a (Prp9 and Prp11) and SF3b (Hsh155 and Cus1) proteins in the head domain and two U4/U6 snRNP proteins (Prp3 and Lsm4) in the neck domain that connects the main body with the head. Thus, we could assign distinct domains of the B complex to the respective snRNPs and provide the first detailed picture of the subunit architecture and protein arrangements of the B complex.
© 2015 The Authors.

Entities:  

Keywords:  B complex; electron microscopy; immunolabelling; protein localisation; spliceosome

Mesh:

Substances:

Year:  2015        PMID: 26582754      PMCID: PMC4687791          DOI: 10.15252/embj.201592022

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


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