| Literature DB >> 29456023 |
Yan Zhang1, Samuel Hong2, Ajchareeya Ruangprasert2, Georgios Skiniotis3, Christine M Dunham4.
Abstract
Structured mRNAs positioned downstream of the ribosomal decoding center alter gene expression by slowing protein synthesis. Here, we solved the cryo-EM structure of the bacterial ribosome bound to an mRNA containing a 3' stem loop that regulates translation. Unexpectedly, the E-site tRNA adopts two distinct orientations. In the first structure, normal interactions with the 50S and 30S E site are observed. However, in the second structure, although the E-site tRNA makes normal interactions with the 50S E site, its anticodon stem loop moves ∼54 Å away from the 30S E site to interact with the 30S head domain and 50S uL5. This position of the E-site tRNA causes the uL1 stalk to adopt a more open conformation that likely represents an intermediate state during E-site tRNA dissociation. These results suggest that structured mRNAs at the entrance channel restrict 30S subunit movement required during translation to slow E-site tRNA dissociation.Entities:
Keywords: RNA structure; cryo-EM; protein synthesis; ribosome; stem loop; translational control
Mesh:
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Year: 2018 PMID: 29456023 PMCID: PMC5842130 DOI: 10.1016/j.str.2018.01.013
Source DB: PubMed Journal: Structure ISSN: 0969-2126 Impact factor: 5.006