Blobel Günter
Laboratory of Cell Biology, The Rockefeller University Howard Hughes Medical Institute, New York, New York 10065, USA.
Cold Spring Harb Symp Quant Biol. 2010;75:545-54. doi: 10.1101/sqb.2010.75.004. Epub 2010 Nov 3.
In evolution, the nuclear envelope (NE) arose from the prokaryotic plasma membrane. NE-associated structures, such as nuclear pore complexes (NPCs), the nuclear lamina, and nuclear envelope junctions (NEJs), have evolved to organize, among other things, chromatids within the three-dimensional space of the nucleus. NEJs represent patches of distinct integral membrane proteins of the outer and inner NE membranes, which, by interacting through conserved domains in the perinuclear space, closely align the two NE membranes. In a nuts-and-bolts configuration, the NEJs are linked to repetitive heterochromatin segments of chromatids on their nuclear side and to cytoskeletal elements on their cytoplasmic side. Cytoskeleton-generated mechanical forces are thereby effectively buffered to allow movement of nuclei in the viscous cytoplasm without disrupting the NE. Moreover, these same mechanical forces could generate distortions within the nucleus to facilitate chromatid fluctuations required for DNA repair, replication, and transcription. NPCs are the only route for bidirectional macromolecular transport between the cytoplasm and the nucleus. They also interact with euchromatin segments of chromatids. Thus far, crystallographic analyses of some nucleoporin contact sites suggest considerable plasticity. This flexibility has likely coevolved to not only buffer the mechanical forces propagated from the NEJs to the network of the more than 500 nucleoporins that make up a single NPC, but also impart fluctuations to NPC conformations for transporting large cargoes.
在进化过程中,核膜(NE)起源于原核生物的质膜。与核膜相关的结构,如核孔复合体(NPC)、核纤层和核膜连接(NEJ),已经进化以在细胞核的三维空间内组织染色单体等物质。核膜连接代表外核膜和内核膜中不同的整合膜蛋白斑块,它们通过在核周空间中的保守结构域相互作用,使两层核膜紧密对齐。在一种基本结构中,核膜连接在其核侧与染色单体的重复异染色质片段相连,在其胞质侧与细胞骨架元件相连。由此,细胞骨架产生的机械力得到有效缓冲,使细胞核能够在粘性细胞质中移动而不破坏核膜。此外,这些相同的机械力可能会在细胞核内产生变形,以促进DNA修复、复制和转录所需的染色单体波动。核孔复合体是细胞质和细胞核之间双向大分子运输的唯一途径。它们还与染色单体的常染色质片段相互作用。到目前为止,对一些核孔蛋白接触位点的晶体学分析表明其具有相当大的可塑性。这种灵活性可能是共同进化而来的,不仅用于缓冲从核膜连接传播到构成单个核孔复合体的500多种核孔蛋白网络的机械力,还用于赋予核孔复合体构象波动以运输大型货物。