Bagnat Michel, Simons Kai
Max Planck Institute for Molecular Cell Biology and Genetics, 01307 Dresden, Germany.
Proc Natl Acad Sci U S A. 2002 Oct 29;99(22):14183-8. doi: 10.1073/pnas.172517799. Epub 2002 Oct 8.
Exposure to mating pheromone in haploid Saccharomyces cerevisiae cells results in the arrest of the cell cycle, expression of mating-specific genes, and polarized growth toward the mating partner. Proteins involved in signaling, polarization, cell adhesion, and fusion are localized to the tip of the mating cell (shmoo) where fusion will eventually occur. The mechanisms ensuring the correct targeting and retention of these proteins are poorly understood. Here we show that in pheromone-treated cells, a reorganization of the plasma membrane involving lipid rafts results in the retention of proteins at the tip of the mating projection, segregated from the rest of the membrane. Sphingolipid and ergosterol biosynthetic mutants fail to polarize proteins to the tip of the shmoo and are deficient in mating. Our results show that membrane microdomain clustering at the mating projection is involved in the generation and maintenance of polarity during mating.
在单倍体酿酒酵母细胞中,暴露于交配信息素会导致细胞周期停滞、交配特异性基因表达以及向交配伙伴的极化生长。参与信号传导、极化、细胞黏附和融合的蛋白质定位于交配细胞(接合芽)的尖端,最终融合将在此处发生。确保这些蛋白质正确靶向和保留的机制尚不清楚。在这里,我们表明,在信息素处理的细胞中,涉及脂筏的质膜重组导致蛋白质保留在交配突起的尖端,与膜的其余部分分离。鞘脂和麦角固醇生物合成突变体无法将蛋白质极化到接合芽的尖端,并且在交配方面存在缺陷。我们的结果表明,交配突起处的膜微区聚集参与了交配过程中极性的产生和维持。