Thevissen Karin, Idkowiak-Baldys Jola, Im Yang-Ju, Takemoto Jon, François Isabelle E J A, Ferket Kathelijne K A, Aerts An M, Meert Els M K, Winderickx Joris, Roosen Johnny, Cammue Bruno P A
Centre for Microbial and Plant Genetics, Katholieke Universiteit Leuven, Kasteelpark Arenberg 20, B-3001 Heverlee, Belgium.
FEBS Lett. 2005 Mar 28;579(9):1973-7. doi: 10.1016/j.febslet.2005.02.043.
The antifungal plant defensin DmAMP1 interacts with the fungal sphingolipid mannosyl diinositolphosphoryl ceramide (M(IP)(2)C) and induces fungal growth inhibition. We have identified SKN1, besides the M(IP)(2)C-biosynthesis gene IPT1, as a novel DmAMP1-sensitivity gene in Saccharomyces cerevisiae. SKN1 was previously shown to be a KRE6 homologue, which is involved in beta-1,6-glucan biosynthesis. We demonstrate that a Deltaskn1 mutant lacks M(IP)(2)C. Interestingly, overexpression of either IPT1 or SKN1 complemented the skn1 mutation, conferred sensitivity to DmAMP1, and resulted in M(IP)(2)C levels comparable to the wild type. These results show that SKN1, together with IPT1, is involved in sphingolipid biosynthesis in S. cerevisiae.
抗真菌植物防御素DmAMP1与真菌鞘脂甘露糖基二肌醇磷酸神经酰胺(M(IP)(2)C)相互作用,并诱导真菌生长抑制。除了M(IP)(2)C生物合成基因IPT1外,我们还在酿酒酵母中鉴定出SKN1作为一个新的DmAMP1敏感性基因。SKN1先前被证明是KRE6的同源物,参与β-1,6-葡聚糖的生物合成。我们证明,Δskn1突变体缺乏M(IP)(2)C。有趣的是,IPT1或SKN1的过表达弥补了skn1突变,赋予了对DmAMP1的敏感性,并导致M(IP)(2)C水平与野生型相当。这些结果表明,SKN1与IPT1一起参与了酿酒酵母中的鞘脂生物合成。