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Stochastic galactokinase expression underlies GAL gene induction in a GAL 3 mutant of Saccharomyces cerevisiae
Author(s) -
Kar Rajesh Kumar,
Qureshi Mohd. Tanvir,
DasAdhikari Akshay Kumar,
Zahir Taiyeb,
Venkatesh Kareenhalli V.,
Bhat Paike Jayadeva
Publication year - 2014
Publication title -
the febs journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 204
eISSN - 1742-4658
pISSN - 1742-464X
DOI - 10.1111/febs.12741
Subject(s) - galactokinase , galactose , complementation , saccharomyces cerevisiae , biology , mutant , population , gene , phenotype , locus (genetics) , genetics , biochemistry , demography , escherichia coli , sociology
GAL 1 and GAL 3 are paralogous signal transducers that functionally inactivate Gal80p to activate the Gal4p‐dependent transcriptional activation of GAL genes in Saccharomyces cerevisiae in response to galactose. Unlike a wild‐type strain, the gal3∆ strain shows delayed growth kinetics as a result of the signaling function of GAL 1 . The mechanism ensuring that GAL 1 is eventually expressed to turn on the GAL switch in the gal3∆ strain remains a paradox. Using galactose and histidine growth complementation assays, we demonstrate that 0.3% of the gal3∆ cell population responds to galactose. This is corroborated by flow cytometry and microscopic analysis. The galactose responders and nonresponders isolated from the galactose‐adapted population attain the original bimodal state and this phenotype is found to be as hard wired as a genetic trait. Computational analysis suggests that the log‐normal distribution in GAL 4 synthesis can lead to bimodal expression of GAL 80 , resulting in the bimodal expression of GAL genes. Heterozygosity at the GAL 80 but not at the GAL 1 , GAL 2 or GAL 4 locus alters the extent of bimodality of the gal3∆ cell population. We suggest that the asymmetric expression pattern between GAL 1 and GAL 3 results in the ability of S. cerevisiae to activate the GAL pathway by conferring nongenetic heterogeneity.