Larijani B, Barona T M, Poccia D L
Department of Biology, Amherst College, Amherst, MA 01002, USA.
Biochem J. 2001 Jun 1;356(Pt 2):495-501. doi: 10.1042/0264-6021:3560495.
PtdIns is a minor membrane phospholipid that is important in signal transduction. Recently, derivatives of PtdIns phosphorylated at the 3-position of the inositol ring have been implicated in the regulation of constitutive membrane traffic and in membrane fusion events. Assembly of the nuclear envelope (NE), a crucial step in the progress of mitosis, is also likely to involve membrane fusion reactions. We therefore investigated the role of PtdIns and phosphoinositide 3-kinase (PI-3K) activity in NE formation in vitro. GTP-induced NE formation was blocked by wortmannin and LY294002, two specific inhibitors of PI-3K, suggesting a role for PtdIns phosphorylated at the 3-position. PtdIns-specific phospholipase C mimicked GTP hydrolysis as an inducer of NE formation. This induction was dependent on a membrane vesicle subfraction (MV1) that was highly enriched in PtdIns, as determined by heteronuclear two-dimensional NMR spectroscopy. On the basis of these results, we suggest that the MV1 population serves as a source of membranes rich in PtdIns that might facilitate fusion, possibly through the production of the membrane-destabilizing lipid diacylglycerol.
磷脂酰肌醇(PtdIns)是一种在信号转导中起重要作用的微量膜磷脂。最近,在肌醇环3位磷酸化的PtdIns衍生物与组成型膜运输的调节以及膜融合事件有关。核膜(NE)的组装是有丝分裂进程中的关键步骤,也可能涉及膜融合反应。因此,我们研究了PtdIns和磷酸肌醇3激酶(PI-3K)活性在体外NE形成中的作用。GTP诱导的NE形成被渥曼青霉素和LY294002(两种PI-3K的特异性抑制剂)阻断,这表明3位磷酸化的PtdIns发挥了作用。PtdIns特异性磷脂酶C模拟GTP水解作为NE形成的诱导剂。这种诱导依赖于一种膜囊泡亚组分(MV1),通过异核二维核磁共振光谱测定,该亚组分富含PtdIns。基于这些结果,我们认为MV1群体作为富含PtdIns的膜源,可能通过产生破坏膜稳定性的脂质二酰基甘油来促进融合。