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Localization of Gln3-GFP and Gat1-GFP in wild type and pph21Δpph22Δ mutant strains in response to rapamycin. The experimental format and data presentation were the same as those in Fig. 7 with two exceptions. First, the strains used as transformation recipients were wild type (TB50; panels A, B, E, and F) and pph21Δpph22Δ (FV239; panels C, D, G, and H). Second, rapamycin replaced methionine sulfoximine as the inhibitor added to the cultures.
