Basic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Basic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA
J Cell Sci. 2020 Jul 8;133(13):jcs243576. doi: 10.1242/jcs.243576.
Nuclear envelope (NE) budding is a recently described phenomenon wherein large macromolecular complexes are packaged inside the nucleus and extruded through the nuclear membranes. Although a general outline of the cellular events occurring during NE budding is now in place, little is yet known about the molecular machinery and mechanisms underlying the physical aspects of NE bud formation. Using a multidisciplinary approach, we identify Wash, its regulatory complex (SHRC), capping protein and Arp2/3 as new molecular components involved in the physical aspects of NE bud formation in a model system. Interestingly, Wash affects NE budding in two ways: indirectly through general nuclear lamina disruption via an SHRC-independent interaction with Lamin B leading to inefficient NE bud formation, and directly by blocking NE bud formation along with its SHRC, capping protein and Arp2/3. In addition to NE budding emerging as an important cellular process, it shares many similarities with herpesvirus nuclear egress mechanisms, suggesting new avenues for exploration in both normal and disease biology.
核膜(NE)出芽是最近描述的一种现象,其中大分子复合物被包装在核内,并通过核膜挤出。尽管现在已经大致了解了 NE 出芽过程中发生的细胞事件,但对于形成 NE 芽的物理方面的分子机制和机制还知之甚少。我们采用多学科方法,在模型系统中鉴定 Wash、其调节复合物 (SHRC)、盖帽蛋白和 Arp2/3 作为参与 NE 芽形成的物理方面的新分子成分。有趣的是,Wash 通过两种方式影响 NE 出芽:通过与核纤层蛋白 B 的独立于 SHRC 的相互作用间接破坏核纤层,导致 NE 出芽效率低下,以及直接与 SHRC、盖帽蛋白和 Arp2/3 一起阻止 NE 出芽。除了 NE 出芽作为一个重要的细胞过程出现之外,它还与疱疹病毒核外溢机制有许多相似之处,这为正常和疾病生物学的探索提供了新的途径。