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. 2014 Jun 21;42(13):8537–8555. doi: 10.1093/nar/gku550

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© The Author(s) 2014. Published by Oxford University Press on behalf of Nucleic Acids Research.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Figure 2. — Truncation of Rps5 46 N-terminal amino acid residues confers leaky scanning phenotype. Expression of reporter GCN4-lacZ constructs. rps5-Δ0 and isogenic rps5-Δ1-13, rps5-Δ1-24, rps5-Δ1-30, rps5-Δ1-46 strains were transformed with (A) p227 containing uORFs less GCN4 mRNA leader; (B) p209 containing uORF1; (C) p226 containing only uORF4 and (D) pM226 containing uORF1 extended into GCN4 ORF. β-Galactosidase activity (units) are shown; measured under normal (−SM) and aa starved conditions (+SM) as in Figure 1.