Institut für Biochemie und Molekulare Zellbiologie, Georg-August-Universität Göttingen, 37077 Göttingen, Germany.
Mol Biol Cell. 2010 Oct 1;21(19):3409-20. doi: 10.1091/mbc.E10-03-0230. Epub 2010 Aug 4.
Nuclear shape changes are observed during a variety of developmental processes, pathological conditions, and ageing. The mechanisms underlying nuclear shape changes in the above-mentioned situations have mostly remained unclear. To address the molecular mechanism behind nuclear shape changes, we analyzed how the farnesylated nuclear envelope proteins Kugelkern and lamin Dm0 affect the structure of the nuclear membrane. We found that Kugelkern and lamin Dm0 affect nuclear shape without requiring filament formation or the presence of a classical nuclear lamina. We also could show that the two proteins do not depend on a group of selected inner nuclear membrane proteins for their localization to the nuclear envelope. Surprisingly, we found that farnesylated Kugelkern and lamin Dm0 protein constructs change the morphology of protein-free liposomes. Based on these findings, we propose that farnesylated proteins of the nuclear membrane induce nuclear shape changes by being asymmetrically inserted into the phospholipid bilayer via their farnesylated C-terminal part.
核形状变化在多种发育过程、病理条件和衰老过程中观察到。在上述情况下,核形状变化的潜在机制在很大程度上仍不清楚。为了解决核形状变化背后的分子机制,我们分析了法呢基化核包膜蛋白 Kugelkern 和 lamin Dm0 如何影响核膜的结构。我们发现 Kugelkern 和 lamin Dm0 影响核形状,而不需要形成细丝或存在经典的核层。我们还可以表明,这两种蛋白质的定位并不依赖于一组选定的内核膜蛋白。令人惊讶的是,我们发现法呢基化的 Kugelkern 和 lamin Dm0 蛋白结构改变了无蛋白脂质体的形态。基于这些发现,我们提出核膜的法呢基化蛋白通过其法呢基化的 C 末端不对称插入磷脂双层来诱导核形状变化。