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新型含重复序列的酵母核孔蛋白RAT7/NUP159的条件等位基因会导致mRNA输出迅速停止以及核孔复合体的可逆聚集。

A conditional allele of the novel repeat-containing yeast nucleoporin RAT7/NUP159 causes both rapid cessation of mRNA export and reversible clustering of nuclear pore complexes.

作者信息

Gorsch L C, Dockendorff T C, Cole C N

机构信息

Department of Biochemistry, Dartmouth Medical School, Hanover, New Hampshire 03755, USA.

出版信息

J Cell Biol. 1995 May;129(4):939-55. doi: 10.1083/jcb.129.4.939.

Abstract

In a screen for Saccharomyces cerevisiae genes required for nucleocytoplasmic transport of messenger RNA, we identified the RAT7 gene (ribonucleic acid trafficking), which encodes an essential protein of 1,460 amino acids. Rat7p is located at the nuclear rim in a punctate pattern characteristic of nucleoporins. Furthermore, the central third of Rat7p contains 22 XXFG and three XFXFG degenerate repeats that are similar to signature GLFG and XFXFG repeats present in a majority of yeast and some mammalian nucleoporins sequenced to date. Shift of a strain bearing the temperature-sensitive rat7-1 allele from 23 degrees C to 37 degrees C resulted in rapid (within 15 minutes) cessation of mRNA export, but did not cause concomitant cytoplasmic accumulation of a reporter protein bearing a nuclear localization signal. This suggests that Rat7p may play a direct role in nucleocytoplasmic export of RNA. Immunofluorescence and thin section electron microscopy revealed that in rat7-1 cells grown at 23 degrees C, the majority of nuclear pore complexes (NPCs) were clustered on one side of the nucleus. No ultrastructural abnormalities of the nuclear envelope were seen. Interestingly, shifting rat7-1 cells to 37 degrees C for 1 h caused the NPCs to disperse, restoring near wild-type NPC distribution. After this temperature shift, the mutant Rat7p was no longer detectable by immunofluorescence.

摘要

在一项针对信使核糖核酸核质转运所需的酿酒酵母基因的筛选中,我们鉴定出了RAT7基因(核糖核酸运输基因),它编码一种由1460个氨基酸组成的必需蛋白质。Rat7p以核孔蛋白特有的点状模式定位于核边缘。此外,Rat7p的中央三分之一区域包含22个XXFG和3个XFXFG简并重复序列,这些序列与大多数已测序的酵母和一些哺乳动物核孔蛋白中存在的标志性GLFG和XFXFG重复序列相似。携带温度敏感型rat7-1等位基因的菌株从23℃转移到37℃后,mRNA输出迅速(15分钟内)停止,但并未导致携带核定位信号的报告蛋白在细胞质中积累。这表明Rat7p可能在RNA的核质输出中起直接作用。免疫荧光和超薄切片电子显微镜显示,在23℃下生长的rat7-1细胞中,大多数核孔复合体(NPC)聚集在细胞核的一侧。未观察到核膜的超微结构异常。有趣的是,将rat7-1细胞转移到37℃1小时会导致NPC分散,恢复到接近野生型的NPC分布。温度转变后,通过免疫荧光无法再检测到突变的Rat7p。

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