Cohen Merav, Feinstein Naomi, Wilson Katherine L, Gruenbaum Yosef
Department of Genetics, The Institute of Life Sciences, The Hebrew University of Jerusalem, Jerusalem, 91904 Israel.
Mol Biol Cell. 2003 Oct;14(10):4230-7. doi: 10.1091/mbc.e03-04-0260. Epub 2003 Jul 11.
Gp210 is an evolutionarily conserved membrane protein of the nuclear pore complex (NPC). We studied the phenotypes produced by RNAi-induced downregulation of gp210 in both human (HeLa) cells and Caenorhabditis elegans embryos. HeLa cell viability requires Gp210 activity. The dying cells accumulated clustered NPCs and aberrant membrane structures at the nuclear envelope, suggesting that gp210 is required directly or indirectly for nuclear pore formation and dilation as well as the anchoring or structural integrity of mature NPCs. Essential roles for gp210 were confirmed in C. elegans, where RNAi-induced reduction of gp210 caused embryonic lethality. The nuclear envelopes of embryos with reduced gp210 also had aberrant nuclear membrane structures and clustered NPCs, confirming that gp210 plays critical roles at the nuclear membrane through mechanisms that are conserved from nematodes to humans.
Gp210是核孔复合体(NPC)中一种进化上保守的膜蛋白。我们研究了RNA干扰诱导的gp210在人(HeLa)细胞和秀丽隐杆线虫胚胎中表达下调所产生的表型。HeLa细胞的存活需要Gp210的活性。垂死的细胞在核膜处积累了聚集的核孔复合体和异常的膜结构,这表明gp210对于核孔的形成和扩张以及成熟核孔复合体的锚定或结构完整性直接或间接是必需的。在秀丽隐杆线虫中证实了gp210的重要作用,RNA干扰诱导的gp210减少导致胚胎致死。gp210减少的胚胎的核膜也有异常的核膜结构和聚集的核孔复合体,证实了gp210通过从线虫到人类保守的机制在核膜上发挥关键作用。