Ribosome A and P sites revealed by length analysis of ribosome profiling data.

Abstract:

:The high-throughput sequencing of nuclease-protected mRNA fragments bound to ribosomes, a technique known as ribosome profiling, quantifies the relative frequencies with which different regions of transcripts are translated. This technique has revealed novel translation initiation sites with unprecedented scope and has furthered investigations into the connections between codon biases and translation rates. Yet the location of the codon being decoded in ribosome footprints is still unknown, and has been complicated by the recent observation of footprints with non-canonical lengths. Here we show how taking into account the variations in ribosome footprint lengths can reveal the ribosome aminoacyl (A) and peptidyl (P) site locations. These location assignments are in agreement with the proposed mechanisms for various ribosome pauses and further enhance the resolution of the profiling data. We also show that GC-rich motifs at the 5' ends of footprints are found in yeast, calling into question the anti-Shine-Dalgarno effect's role in ribosome pausing.

journal_name

Nucleic Acids Res

journal_title

Nucleic acids research

authors

Martens AT,Taylor J,Hilser VJ

doi

10.1093/nar/gkv200

subject

Has Abstract

pub_date

2015-04-20 00:00:00

pages

3680-7

issue

7

eissn

0305-1048

issn

1362-4962

pii

gkv200

journal_volume

43

pub_type

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