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The GAL genetic switch: visualisation of the interacting proteins by split-EGFP bimolecular fluorescence complementation

✍ Scribed by Emma Barnard; David J. Timson


Book ID
102393754
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
239 KB
Volume
51
Category
Article
ISSN
0233-111X

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✦ Synopsis


Abstract

A split‐EGFP bimolecular fluorescence complementation assay was used to visualise and locate three interacting pairs of proteins from the GAL genetic switch of the budding yeast, Saccharomyces cerevisiae. Both the Gal4p‐Gal80p and Gal80p‐Gal3p pairs were found to be located in the nucleus under inducing conditions. However, the Gal80p‐Gal1p complex was located throughout the cell. These results support recent work establishing an initial interaction between Gal3p and Gal80p occurring in the nucleus. Labelling of all three protein pairs impaired the growth of the yeast strains and resulted in reduced galactokinase activity in cell extracts. The most likely cause of this impairment is decreased dissociation rates of the complexes, caused by the essentially irreversible reassembly of the EGFP fragments. This suggests that a fully functional GAL genetic switch requires dynamic interactions between the protein components. These results also highlight the need for caution in the interpretation of in vivo split‐EGFP experiments. (© 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)