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. 2001 Nov 15;20(22):6453–6463. doi: 10.1093/emboj/20.22.6453

graphic file with name cde606f1.jpg

Fig. 1. Sequences of the 5′ leader regions of GCN4–LUC genes used in this study. The sequence shown begins with the T7 RNA polymerase-binding site and ends within the LUC coding region. The 5′ and 3′ boundaries of the wild-type GCN4 sequence are boxed. GCN4 uORFs and the GCN4 ATGORF are shown in bold and mutations are indicated below the wild-type sequence. Horizontal arrows below the sequence indicate the sequences for which the reverse complements were synthesized and used as primers ZW4 and ZW18 for toeprint analysis.