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Cell Res. 2014 Jul;24(7):842-51. doi: 10.1038/cr.2014.74. Epub 2014 Jun 6.

Ribosome profiling reveals sequence-independent post-initiation pausing as a signature of translation.

Author information

1
1] Division of Nutritional Sciences, Cornell University, Ithaca, NY 14853, USA [2] Department of Infectious Diseases, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200025, China.
2
Division of Nutritional Sciences, Cornell University, Ithaca, NY 14853, USA.
3
Graduate Field of Genetics, Genomics and Development, Cornell University, Ithaca, NY 14853, USA.

Abstract

The journey of a newly synthesized polypeptide starts in the peptidyltransferase center of the ribosome, from where it traverses the exit tunnel. The interior of the ribosome exit tunnel is neither straight nor smooth. How the ribosome dynamics in vivo is influenced by the exit tunnel is poorly understood. Genome-wide ribosome profiling in mammalian cells reveals elevated ribosome density at the start codon and surprisingly the downstream 5th codon position as well. We found that the highly focused ribosomal pausing shortly after initiation is attributed to the geometry of the exit tunnel, as deletion of the loop region from ribosome protein L4 diminishes translational pausing at the 5th codon position. Unexpectedly, the ribosome variant undergoes translational abandonment shortly after initiation, suggesting that there exists an obligatory step between initiation and elongation commitment. We propose that the post-initiation pausing of ribosomes represents an inherent signature of the translation machinery to ensure productive translation.

PMID:
24903108
PMCID:
PMC4085768
DOI:
10.1038/cr.2014.74
[Indexed for MEDLINE]
Free PMC Article
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