Petrovic Uros, Sribar Jernej, Matis Maja, Anderluh Gregor, Peter-Katalinić Jasna, Krizaj Igor, Gubensek Franc
Department of Biochemistry and Molecular Biology, Jozef Stefan Institute, SI-1000 Ljubljana, Slovenia.
Biochem J. 2005 Oct 15;391(Pt 2):383-8. doi: 10.1042/BJ20050417.
Ammodytoxin (Atx), an sPLA2 (secretory phospholipase A2), binds to g and e isoforms of porcine 14-3-3 proteins in vitro. 14-3-3 proteins are evolutionarily conserved eukaryotic regulatory proteins involved in a variety of biological processes, including cell-cycle regulation. We have now shown that Atx binds to yeast 14-3-3 proteins with an affinity similar to that for the mammalian isoforms. Thus yeast Saccharomyces cerevisiae can be used as a model eukaryotic cell, which lacks endogenous phospholipases A2, to assess the in vivo relevance of this interaction. Atx was expressed in yeast cells and shown to be biologically active inside the cells. It inhibited G2 cell-cycle arrest in yeast, which is regulated by 14-3-3 proteins. Interference with the cell cycle indicates a possible mechanism by which sPLA2s are able to cause the opposing effects, proliferation and apoptosis, in mammalian cells.
沙蚕毒素(Atx)是一种分泌型磷脂酶A2(sPLA2),在体外可与猪14-3-3蛋白的g和e亚型结合。14-3-3蛋白是进化上保守的真核调节蛋白,参与包括细胞周期调控在内的多种生物学过程。我们现已表明,Atx与酵母14-3-3蛋白的结合亲和力与哺乳动物亚型相似。因此,酿酒酵母可作为缺乏内源性磷脂酶A2的真核细胞模型,用于评估这种相互作用在体内的相关性。Atx在酵母细胞中表达,并显示在细胞内具有生物活性。它抑制酵母中的G2期细胞周期阻滞,而这一过程受14-3-3蛋白调控。对细胞周期的干扰表明了sPLA2能够在哺乳动物细胞中产生增殖和凋亡这两种相反作用的一种可能机制。