Hf. Shen et W. Dowhan, REGULATION OF PHOSPHATIDYLGLYCEROPHOSPHATE SYNTHASE LEVELS IN SACCHAROMYCES-CEREVISIAE, The Journal of biological chemistry, 273(19), 1998, pp. 11638-11642
The PGS1 gene of Saccharomyces cerevisiae encodes phosphatidylglycerop
hosphate (PG-P) synthase. PG-P synthase activity is regulated by facto
rs affecting mitochondrial development and through cross-pathway contr
ol by inositol. The molecular mechanism of this regulation was examine
d by using a reporter gene under control of the PGS1 gene promoter (P-
PGS1-lacZ). Gene expression subject to carbon source regulation was mo
nitored both at steady-state level and during the switch between diffe
rent carbon sources. Cells grown in a non-fermentable carbon source ha
d beta-galactosidase levels 3-fold higher than those grown in glucose.
A shift from glucose to lactate rapidly raised the level of gene expr
ession, whereas a shift back to glucose had the opposite effect. In ei
ther a pgs1 null mutant or a rho mutant grown in glucose, P-PGS1-lacZ
expression was 30-50% of the level in wild type cells. Addition of ino
sitol to the growth medium resulted in a 2-3-fold reduction in gene ex
pression in wild type cells. In ino2 and ino8 mutants, gene expression
was greatly reduced and was not subject to inositol regulation consis
tent with inositol repression being dependent on the INO2 and INO4 reg
ulatory genes. P(PGS1)-lacZ expression was elevated in a cds1 null mut
ant in the presence or absence of inositol, indicating that the capaci
ty to synthesize CDP-diacylglycerol affects gene expression. Lack of c
ardiolipin synthesis (cls1 null mutant) had no effect on reporter gene
expression.