Figure 5.
Figure 5. LRM2 is the functional nuclear export signal in c-IAP1. (A) Fluorescence microscopy analysis of HeLa cells transfected for 24 hours with constructs encoding wild-type or mutated GFP-c-IAP1 (nuclei were stained with Hoechst 33342). Leucine residues in LRMs (LRM1*: Leu250, Leu254, Leu257; LRM2*: Leu468, Leu472, Leu476, Leu483; LRM3*: Leu556, Leu558, Leu562, Leu565) were replaced by alanine residues using site-directed mutagenesis. *Mutated constructs (magnification ×1000). (B) Western blot analysis of GFP expression in nuclear (N) and cytoplasmic (C) extracts from HeLa cells transfected 24 hours before with indicated constructs.

LRM2 is the functional nuclear export signal in c-IAP1. (A) Fluorescence microscopy analysis of HeLa cells transfected for 24 hours with constructs encoding wild-type or mutated GFP-c-IAP1 (nuclei were stained with Hoechst 33342). Leucine residues in LRMs (LRM1*: Leu250, Leu254, Leu257; LRM2*: Leu468, Leu472, Leu476, Leu483; LRM3*: Leu556, Leu558, Leu562, Leu565) were replaced by alanine residues using site-directed mutagenesis. *Mutated constructs (magnification ×1000). (B) Western blot analysis of GFP expression in nuclear (N) and cytoplasmic (C) extracts from HeLa cells transfected 24 hours before with indicated constructs.

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