Ribosome profiling of mouse embryonic stem cells reveals the complexity and dynamics of mammalian proteomes.

Project: Aim 2
Citation: Ingolia NT, Lareau LF, Weissman JS 
Journal: Cell
Publication Date: Nov. 11 2011
Paper Name: Chevrier.Cell.2011.10.022
Link: http://dx.doi.org/10.1016/j.cell.2011.10.002

Abstract: The ability to sequence genomes has far outstripped approaches for deciphering the information they encode. Here we present a suite of techniques, based on ribosome profiling (the deep sequencing of ribosome-protected mRNA fragments), to provide genome-wide maps of protein synthesis as well as a pulse-chase strategy for determining rates of translation elongation. We exploit the propensity of harringtonine to cause ribosomes to accumulate at sites of translation initiation together with a machine learning algorithm to define protein products systematically. Analysis of translation in mouse embryonic stem cells reveals thousands of strong pause sites and unannotated translation products. These include amino-terminal extensions and truncations and upstream open reading frames with regulatory potential, initiated at both AUG and non-AUG codons, whose translation changes after differentiation. We also define a class of short, polycistronic ribosome-associated coding RNAs (sprcRNAs) that encode small proteins. Our studies reveal an unanticipated complexity to mammalian proteomes.