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1
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.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。
J Cell Biol. 1995 May;129(4):939-55. doi: 10.1083/jcb.129.4.939.
2
The product of the Saccharomyces cerevisiae RSS1 gene, identified as a high-copy suppressor of the rat7-1 temperature-sensitive allele of the RAT7/NUP159 nucleoporin, is required for efficient mRNA export.酿酒酵母RSS1基因的产物被鉴定为RAT7/NUP159核孔蛋白的大鼠7-1温度敏感等位基因的高拷贝抑制因子,它是高效mRNA输出所必需的。
Mol Biol Cell. 1996 Oct;7(10):1601-21. doi: 10.1091/mbc.7.10.1601.
3
Nuclear pore complex clustering and nuclear accumulation of poly(A)+ RNA associated with mutation of the Saccharomyces cerevisiae RAT2/NUP120 gene.与酿酒酵母RAT2/NUP120基因突变相关的核孔复合体聚集及多聚腺苷酸(poly(A)+)RNA的核内积累
J Cell Biol. 1995 Dec;131(6 Pt 2):1677-97. doi: 10.1083/jcb.131.6.1677.
4
Mutation or deletion of the Saccharomyces cerevisiae RAT3/NUP133 gene causes temperature-dependent nuclear accumulation of poly(A)+ RNA and constitutive clustering of nuclear pore complexes.酿酒酵母RAT3/NUP133基因的突变或缺失会导致聚腺苷酸(poly(A)+)RNA在温度依赖性条件下在细胞核中积累,以及核孔复合体的组成性聚集。
Mol Biol Cell. 1995 Apr;6(4):401-417. doi: 10.1091/mbc.6.4.401.
5
A novel nuclear pore protein Nup133p with distinct roles in poly(A)+ RNA transport and nuclear pore distribution.一种新型核孔蛋白Nup133p在多聚腺苷酸(poly(A)+)RNA转运和核孔分布中具有不同作用。
EMBO J. 1994 Dec 15;13(24):6062-75. doi: 10.1002/j.1460-2075.1994.tb06953.x.
6
A structure/function analysis of Rat7p/Nup159p, an essential nucleoporin of Saccharomyces cerevisiae.酿酒酵母必需核孔蛋白Rat7p/Nup159p的结构/功能分析。
J Cell Sci. 1997 Dec;110 ( Pt 23):2987-99. doi: 10.1242/jcs.110.23.2987.
7
Npp106p, a Schizosaccharomyces pombe nucleoporin similar to Saccharomyces cerevisiae Nic96p, functionally interacts with Rae1p in mRNA export.Npp106p是一种与酿酒酵母Nic96p相似的粟酒裂殖酵母核孔蛋白,在mRNA输出过程中与Rae1p发生功能相互作用。
Mol Cell Biol. 1997 Dec;17(12):7047-60. doi: 10.1128/MCB.17.12.7047.
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Functional characterization of a Nup159p-containing nuclear pore subcomplex.含Nup159p的核孔亚复合体的功能特性
Mol Biol Cell. 1998 Dec;9(12):3475-92. doi: 10.1091/mbc.9.12.3475.
9
Nuclear transport defects and nuclear envelope alterations are associated with mutation of the Saccharomyces cerevisiae NPL4 gene.核转运缺陷和核膜改变与酿酒酵母NPL4基因的突变有关。
Mol Biol Cell. 1996 Nov;7(11):1835-55. doi: 10.1091/mbc.7.11.1835.
10
Nup145p is required for nuclear export of mRNA and binds homopolymeric RNA in vitro via a novel conserved motif.Nup145p是mRNA核输出所必需的,并且在体外通过一个新的保守基序与同聚RNA结合。
Cell. 1994 Jul 29;78(2):275-89. doi: 10.1016/0092-8674(94)90297-6.

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3
Dbp5 associates with RNA-bound Mex67 and Nab2 and its localization at the nuclear pore complex is sufficient for mRNP export and cell viability.Dbp5 与 RNA 结合的 Mex67 和 Nab2 相关联,其在核孔复合体中的定位足以促进 mRNP 输出和细胞活力。
PLoS Genet. 2020 Oct 1;16(10):e1009033. doi: 10.1371/journal.pgen.1009033. eCollection 2020 Oct.
4
A nuclear role for the DEAD-box protein Dbp5 in tRNA export.Dbp5 蛋白在 tRNA 输出中的核作用。
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A Nuclear Export Block Triggers the Decay of Newly Synthesized Polyadenylated RNA.核输出阻断触发新合成的多聚腺苷酸化 RNA 的降解。
Cell Rep. 2018 Aug 28;24(9):2457-2467.e7. doi: 10.1016/j.celrep.2018.07.103.
6
Exportin Crm1 is repurposed as a docking protein to generate microtubule organizing centers at the nuclear pore.CRM1 输出蛋白被重新用作对接蛋白,在核孔处生成微管组织中心。
Elife. 2018 May 29;7:e33465. doi: 10.7554/eLife.33465.
7
Saccharomyces cerevisiae Gle2/Rae1 is involved in septin organization, essential for cell cycle progression.酿酒酵母Gle2/Rae1参与隔膜蛋白组织,这对细胞周期进程至关重要。
Yeast. 2017 Nov;34(11):459-470. doi: 10.1002/yea.3249. Epub 2017 Sep 28.
8
mRNA quality control is bypassed for immediate export of stress-responsive transcripts.mRNA质量控制被绕过,以便应激反应性转录本立即输出。
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9
Altered RNA processing and export lead to retention of mRNAs near transcription sites and nuclear pore complexes or within the nucleolus.RNA加工和输出的改变导致mRNA滞留在转录位点、核孔复合体附近或核仁内。
Mol Biol Cell. 2016 Sep 1;27(17):2742-56. doi: 10.1091/mbc.E16-04-0244. Epub 2016 Jul 6.
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Interactome Mapping Reveals the Evolutionary History of the Nuclear Pore Complex.相互作用组图谱揭示了核孔复合体的进化史。
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本文引用的文献

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Pores for thought: nuclear pore complex proteins.思考的孔隙:核孔复合体蛋白
Trends Cell Biol. 1994 Oct;4(10):357-65. doi: 10.1016/0962-8924(94)90085-x.
2
Nuclear pore complex antigens delineate nuclear envelope dynamics in vegetative and conjugating Saccharomyces cerevisiae.核孔复合体抗原描绘了营养型和接合型酿酒酵母中的核膜动态变化。
Yeast. 1993 Mar;9(3):235-49. doi: 10.1002/yea.320090304.
3
NUP2, a novel yeast nucleoporin, has functional overlap with other proteins of the nuclear pore complex.NUP2是一种新型酵母核孔蛋白,与核孔复合体的其他蛋白质存在功能重叠。
Mol Biol Cell. 1993 Feb;4(2):209-22. doi: 10.1091/mbc.4.2.209.
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A nuclear pore complex protein that contains zinc finger motifs, binds DNA, and faces the nucleoplasm.一种含有锌指基序、结合DNA且面向核质的核孔复合体蛋白。
Cell. 1993 Jan 15;72(1):29-38. doi: 10.1016/0092-8674(93)90047-t.
5
An integral membrane protein of the pore membrane domain of the nuclear envelope contains a nucleoporin-like region.核被膜孔膜结构域的一种整合膜蛋白包含一个核孔蛋白样区域。
J Cell Biol. 1993 Aug;122(3):513-21. doi: 10.1083/jcb.122.3.513.
6
Architecture of the Xenopus nuclear pore complex revealed by three-dimensional cryo-electron microscopy.三维冷冻电子显微镜揭示非洲爪蟾核孔复合体的结构
J Cell Biol. 1993 Jul;122(1):1-19. doi: 10.1083/jcb.122.1.1.
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Isolation of the yeast nuclear pore complex.酵母核孔复合体的分离
J Cell Biol. 1993 Nov;123(4):771-83. doi: 10.1083/jcb.123.4.771.
8
NUP145 encodes a novel yeast glycine-leucine-phenylalanine-glycine (GLFG) nucleoporin required for nuclear envelope structure.NUP145编码一种新型酵母甘氨酸-亮氨酸-苯丙氨酸-甘氨酸(GLFG)核孔蛋白,它是核膜结构所必需的。
J Cell Biol. 1994 Jun;125(5):955-69. doi: 10.1083/jcb.125.5.955.
9
POM152 is an integral protein of the pore membrane domain of the yeast nuclear envelope.POM152是酵母核膜孔膜结构域的一种整合蛋白。
J Cell Biol. 1994 Apr;125(1):31-42. doi: 10.1083/jcb.125.1.31.
10
Nup145p is required for nuclear export of mRNA and binds homopolymeric RNA in vitro via a novel conserved motif.Nup145p是mRNA核输出所必需的,并且在体外通过一个新的保守基序与同聚RNA结合。
Cell. 1994 Jul 29;78(2):275-89. doi: 10.1016/0092-8674(94)90297-6.

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.

DOI:10.1083/jcb.129.4.939
PMID:7744966
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2120496/
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。