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Originally published In Press as doi:10.1074/jbc.M603548200 on June 15, 2006

J. Biol. Chem., Vol. 281, Issue 32, 22773-22785, August 11, 2006
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Inositol Induces a Profound Alteration in the Pattern and Rate of Synthesis and Turnover of Membrane Lipids in Saccharomyces cerevisiae*Formula

Maria L. Gaspar, Manuel A. Aregullin, Stephen A. Jesch, and Susan A. Henry1

From the Department of Molecular Biology and Genetics, Cornell University, Ithaca, New York 14853

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 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%. nte1{Delta} 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.


Received for publication, April 25, 2006 , and in revised form, June 7, 2006.

* This work was supported by National Institutes of Health Grant GM-19629 (to S. A. H.). The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

Formula The on-line version of this article (available at http://www.jbc.org) contains supplemental Fig. S1.

1 To whom correspondence should be addressed: College of Agriculture and Life Sciences, Cornell University, 260 Roberts Hall, Ithaca, NY 14853. Tel.: 607-255-2241; Fax: 607-255-3803; E-mail: sah42{at}cornell.edu.


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