Ehrlich Lorna S, Carter Carol A
Department of Molecular Genetics & Microbiology, Stony Brook University, Life Sciences Building Room 248, Stony Brook, NY 11794-5222, USA.
Mol Biol Int. 2012;2012:851670. doi: 10.1155/2012/851670. Epub 2012 Jun 12.
More than a decade has elapsed since the link between the endosomal sorting complex required for transport (ESCRT) machinery and HIV-1 protein trafficking and budding was first identified. L domains in HIV-1 Gag mediate recruitment of ESCRT which function in bud abscission releasing the viral particle from the host cell. Beyond virus budding, the ESCRT machinery is also involved in the endocytic pathway, cytokinesis, and autophagy. In the past few years, the number of non-ESCRT host proteins shown to be required in the assembly process has also grown. In this paper, we highlight the role of recently identified cellular factors that link ESCRT machinery to calcium signaling machinery and we suggest that this liaison contributes to setting the stage for productive ESCRT recruitment and mediation of abscission. Parallel paradigms for non-ESCRT roles in virus budding and cytokinesis will be discussed.
自运输所需内体分选复合体(ESCRT)机制与HIV-1蛋白运输和出芽之间的联系首次被发现以来,已经过去了十多年。HIV-1 Gag中的L结构域介导ESCRT的募集,ESCRT在芽体脱离过程中发挥作用,将病毒颗粒从宿主细胞中释放出来。除了病毒出芽,ESCRT机制还参与内吞途径、胞质分裂和自噬。在过去几年中,已证明在组装过程中需要的非ESCRT宿主蛋白的数量也有所增加。在本文中,我们强调了最近发现的将ESCRT机制与钙信号传导机制联系起来的细胞因子的作用,并提出这种联系有助于为有效的ESCRT募集和芽体脱离的介导奠定基础。将讨论非ESCRT在病毒出芽和胞质分裂中的平行范例。