Webster Brant M, Lusk C Patrick
a Yale School of Medicine ; New Haven , CT , USA.
Nucleus. 2015;6(3):197-202. doi: 10.1080/19491034.2015.1035844. Epub 2015 May 5.
The endosomal sorting complexes required for transport (ESCRT) are best known for their role in sorting ubiquitylated membrane proteins into endosomes. The most ancient component of the ESCRT machinery is ESCRT-III, which is capable of oligomerizing into a helical filament that drives the invagination and scission of membranes aided by the AAA ATPase, Vps4, in several additional subcellular contexts. Our recent study broadens the work of ESCRT-III by identifying its role in a quality control pathway at the nuclear envelope (NE) that ensures the normal biogenesis of nuclear pore complexes (NPCs). Here, we will elaborate on how we envision this mechanism to progress and incorporate ESCRT-III into an emerging model of nuclear pore formation. Moreover, we speculate there are additional roles for the ESCRT-III machinery at the NE that broadly function to ensure its integrity and the maintenance of the nuclear compartment.
转运所需的内体分选复合体(ESCRT)最为人所知的作用是将泛素化的膜蛋白分选到内体中。ESCRT机制中最古老的成分是ESCRT-III,它能够寡聚形成螺旋丝,在几种其他亚细胞环境中,在AAA ATP酶Vps4的辅助下驱动膜的内陷和分裂。我们最近的研究通过确定ESCRT-III在核膜(NE)的质量控制途径中的作用,拓宽了其工作范围,该途径可确保核孔复合体(NPC)的正常生物发生。在此,我们将详细阐述我们设想该机制如何进展,并将ESCRT-III纳入核孔形成的新兴模型。此外,我们推测ESCRT-III机制在核膜处还有其他作用,其广泛功能是确保核膜的完整性和核区室的维持。