부산대학교 도서관

Phosphatidylcholine (PC) is an abundant membrane lipid component in most eukaryotes, including yeast, and has been assigned multiple functions in addition to acting as building block of the lipid bilayer. Here, by isolating S. cerevisiae suppressor mutants that exhibit robust growth in the absence of PC, we show that PC essentiality is subject to cellular evolvability in yeast. The requirement for PC is suppressed by monosomy of chromosome XV or by a point mutation in the ACC1 gene encoding acetyl‐CoA carboxylase. Although these two genetic adaptations rewire lipid biosynthesis in different ways, both decrease Acc1 activity, thereby reducing average acyl chain length. Consistently, soraphen A, a specific inhibitor of Acc1, rescues a yeast mutant with deficient PC synthesis. In the aneuploid suppressor, feedback inhibition of Acc1 through acyl‐CoA produced by fatty acid synthase (FAS) results from upregulation of lipid synthesis. The results show that budding yeast regulates acyl chain length by fine‐tuning the activities of Acc1 and FAS and indicate that PC evolved by benefitting the maintenance of membrane fluidity. SYNOPSIS: Saccharomyces cerevisiae suppressor mutants overcoming choline auxotrophy allow growth in the absence of the major membrane lipid phosphatidylcholine (PC). This study reveals that the interplay between acetyl‐CoA carboxylase (Acc1) and fatty acid synthase (FAS), which regulates lipid acyl chain length, renders PC redundant in such mutant. Most PC‐free choline auxotrophy suppressors are 2n‐1 aneuploids lacking one copy of chromosome XV.Rare diploid suppressor strains contain a homozygous point mutation in the ACC1 gene encoding acetyl‐CoA carboxylase.Aneuploid suppressors rely on feed‐back inhibition of Acc1 by FAS‐derived acyl‐CoA, resulting from up‐regulation of lipid synthesis.Inhibition of Acc1 activity is crucial for suppression by reducing average lipid acyl chain length to maintain membrane fluidity. [ABSTRACT FROM AUTHOR]