Pilecka Iwona, Banach-Orlowska Magdalena, Miaczynska Marta
International Institute of Molecular and Cell Biology, Laboratory of Cell Biology, 4 Ks. Trojdena Street, 02-109 Warsaw, Poland.
Eur J Cell Biol. 2007 Sep;86(9):533-47. doi: 10.1016/j.ejcb.2007.04.004. Epub 2007 Jun 20.
An increasing number of proteins appear to perform multiple, sometimes unrelated functions in the cell. Such moonlighting properties have been recently demonstrated for proteins involved in clathrin-mediated endocytosis. Some clathrin adaptors and endosomal proteins can undergo nucleocytoplasmic shuttling, which is often based on intrinsic sequence motifs and requires active transport mechanisms. Endocytic proteins can associate with nuclear molecules, changing their localization and/or activity and may modulate the levels and specificity of gene transcription. It is not clear how the nuclear and cytoplasmic pools of endocytic proteins are interconnected, or whether these molecules act as nuclear second messengers upon extracellular stimuli, but alike in endocytosis, they seem to form multi-component scaffolding platforms in the nucleus. Added to their endocytic functions, the nuclear roles of Eps15, Epsin1, CALM, HIP1, Dab1/2, beta-arrestins, APPL1/2 and the components of ESCRTs clearly increase the complexity of signaling networks affecting cellular growth, proliferation and homeostasis.
越来越多的蛋白质似乎在细胞中执行多种功能,有时甚至是不相关的功能。最近已证实,参与网格蛋白介导的内吞作用的蛋白质具有这种兼职特性。一些网格蛋白衔接蛋白和内体蛋白可进行核质穿梭,这通常基于内在序列基序,且需要主动运输机制。内吞蛋白可与核分子结合,改变其定位和/或活性,并可能调节基因转录的水平和特异性。目前尚不清楚内吞蛋白的核池和胞质池是如何相互连接的,也不清楚这些分子在细胞外刺激时是否作为核第二信使起作用,但与内吞作用类似,它们似乎在细胞核中形成多组分支架平台。除了其在内吞作用中的功能外,Eps15、Epsin1、CALM、HIP1、Dab1/2、β-抑制蛋白、APPL1/2以及内体分选转运复合体(ESCRT)组分的核作用,显然增加了影响细胞生长、增殖和稳态的信号网络的复杂性。