Abstract
The addition of inositol to actively
growing yeast cultures causes a rapid increase in the rate of synthesis
of phosphatidylinositol
and, simultaneously, triggers changes in the
expression of hundreds of genes. We now demonstrate that the addition of
inositol
to yeast cells growing in the presence of choline
leads to a dramatic reprogramming of cellular lipid synthesis and
turnover.
The response to inositol includes a 5-6-fold
increase in cellular phosphatidylinositol content within a period of 30
min.
The increase in phosphatidylinositol content
appears to be dependent upon fatty acid synthesis. Phosphatidylcholine
turnover
increased rapidly following inositol addition, a
response that requires the participation of Nte1p, an endoplasmic
reticulum-localized
phospholipase B. Mass spectrometry revealed that
the acyl species composition of phosphatidylinositol is relatively
constant
regardless of supplementation with inositol or
choline, whereas phosphatidylcholine acyl species composition is
influenced
by both inositol and choline. In medium containing
inositol, but lacking choline, high levels of
dimyristoylphosphatidylcholine
(DMPC) were detected. Within 60 min following the addition
of inositol, dimyristoylphosphatidylcholine levels had decreased from
∼40% of total phosphatidylcholine to a basal level
of less than 5%. nte1Δ cells grown in the absence of inositol
and in the presence of choline exhibited lower levels of
dimyristoylphosphatidylcholine
than wild type cells grown under these same
conditions, but these levels remained largely constant after the
addition of inositol.
These results are discussed in relationship to
transcriptional regulation known to be linked to lipid metabolism in
yeast.
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