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RNA-蛋白质复合物的核输出动力学。

Nuclear export dynamics of RNA-protein complexes.

机构信息

Delft University of Technology, Faculty of Applied Sciences, Kavli Institute of NanoScience, Department of Bionanoscience, 2628 CJ Delft, The Netherlands.

出版信息

Nature. 2011 Jul 20;475(7356):333-41. doi: 10.1038/nature10318.

DOI:10.1038/nature10318
PMID:21776079
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3154952/
Abstract

The central dogma of molecular biology - DNA makes RNA makes proteins - is a flow of information that in eukaryotes encounters a physical barrier: the nuclear envelope, which encapsulates, organizes and protects the genome. Nuclear-pore complexes, embedded in the nuclear envelope, regulate the passage of molecules to and from the nucleus, including the poorly understood process of the export of RNAs from the nucleus. Recent imaging approaches focusing on single molecules have provided unexpected insight into this crucial step in the information flow. This review addresses the latest studies of RNA export and presents some models for how this complex process may work.

摘要

分子生物学的中心法则——DNA 转录为 RNA 再翻译为蛋白质——是一个信息流,在真核生物中会遇到一个物理屏障:核膜,它包裹、组织和保护基因组。核孔复合物嵌入核膜中,调节分子进出细胞核的过程,包括从细胞核输出 RNA 这一尚未被充分了解的过程。最近专注于单个分子的成像方法为信息流的这一关键步骤提供了意想不到的深入了解。本文综述了 RNA 输出的最新研究,并提出了一些关于这个复杂过程如何运作的模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d61d/3154952/257f6e3feee5/nihms314182f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d61d/3154952/18982809a391/nihms314182f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d61d/3154952/e1b2ad32c8b0/nihms314182f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d61d/3154952/6fe8102e2327/nihms314182f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d61d/3154952/257f6e3feee5/nihms314182f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d61d/3154952/18982809a391/nihms314182f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d61d/3154952/e1b2ad32c8b0/nihms314182f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d61d/3154952/6fe8102e2327/nihms314182f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d61d/3154952/257f6e3feee5/nihms314182f4.jpg

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Subcellular mRNA kinetic modeling reveals nuclear retention as rate-limiting.亚细胞mRNA动力学建模显示核滞留是限速步骤。

本文引用的文献

1
The Dbp5 cycle at the nuclear pore complex during mRNA export II: nucleotide cycling and mRNP remodeling by Dbp5 are controlled by Nup159 and Gle1.核孔复合物中 mRNA 输出过程中的 Dbp5 循环 II:Dbp5 的核苷酸循环和 mRNP 重塑受 Nup159 和 Gle1 控制。
Genes Dev. 2011 May 15;25(10):1065-77. doi: 10.1101/gad.2040611.
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Nature. 2011 Apr 14;472(7342):238-42. doi: 10.1038/nature09862. Epub 2011 Mar 27.
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Linking gene regulation to mRNA production and export.
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RANBP17 Overexpression Restores Nucleocytoplasmic Transport and Ameliorates Neurodevelopment in Induced DYT1 Dystonia Motor Neurons.RANBP17 过表达恢复核质转运并改善诱导性 DYT1 肌张力障碍运动神经元的神经发育。
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Centralspindlin proteins Pavarotti and Tumbleweed along with WASH regulate nuclear envelope budding.中央纺锤体蛋白 Pavarotti 和 Tumbleweed 以及 WASH 共同调节核膜出芽。
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8
CRISPR-dCas13-tracing reveals transcriptional memory and limited mRNA export in developing zebrafish embryos.CRISPR-dCas13 示踪揭示了发育中的斑马鱼胚胎中的转录记忆和有限的 mRNA 输出。
Genome Biol. 2023 Jan 19;24(1):15. doi: 10.1186/s13059-023-02848-6.
9
Pore performance: artificial nanoscale constructs that mimic the biomolecular transport of the nuclear pore complex.孔性能:模拟核孔复合体生物分子转运的人工纳米级结构。
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A nucleoporin, Nup60p, affects the nuclear and cytoplasmic localization of ASH1 mRNA in S. cerevisiae.核孔蛋白 Nup60p 影响酿酒酵母中 ASH1 mRNA 的核质定位。
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