| Literature DB >> 27791167 |
Polly Yingshan Hsu1, Lorenzo Calviello2,3, Hsin-Yen Larry Wu4, Fay-Wei Li1,5,6, Carl J Rothfels5,6, Uwe Ohler2,3, Philip N Benfey7,8.
Abstract
Deep sequencing of ribosome footprints (ribosome profiling) maps and quantifies mRNA translation. Because ribosomes decode mRNA every 3 nt, the periodic property of ribosome footprints could be used to identify novel translated ORFs. However, due to the limited resolution of existing methods, the 3-nt periodicity is observed mostly in a global analysis, but not in individual transcripts. Here, we report a protocol applied to Arabidopsis that maps over 90% of the footprints to the main reading frame and thus offers super-resolution profiles for individual transcripts to precisely define translated regions. The resulting data not only support many annotated and predicted noncanonical translation events but also uncover small ORFs in annotated noncoding RNAs and pseudogenes. A substantial number of these unannotated ORFs are evolutionarily conserved, and some produce stable proteins. Thus, our study provides a valuable resource for plant genomics and an efficient optimization strategy for ribosome profiling in other organisms.Entities:
Keywords: Ribo-seq; ncRNA; ribosome footprint; sORF; translation
Year: 2016 PMID: 27791167 PMCID: PMC5111709 DOI: 10.1073/pnas.1614788113
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205