Visualizing RNA granule transport and translation in living neurons

被引:7
|
作者
Bauer, Karl E. [1 ]
Kiebler, Michael A. [1 ]
Segura, Inmaculada [1 ]
机构
[1] Ludwig Maximilians Univ Munchen, Biomed Ctr, Grosshaderner Str 9, D-82152 Planegg Martinsried, Germany
基金
奥地利科学基金会;
关键词
RNA granules; RNA transport; Neurons; MS2; system; SunTag; Translation; DENDRITIC TARGETING ELEMENT; SINGLE MESSENGER-RNAS; FLUORESCENT-PROTEIN; GENE-EXPRESSION; LIVE CELLS; MONOMERIC RED; LOCALIZATION; DYNAMICS; TRACKING; TRANSCRIPTS;
D O I
10.1016/j.ymeth.2017.06.013
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In polarized cells, such as neurons, the synthesis of an mRNA does not ensure its proper cellular expression. Most mature transcripts require the association with RNA-binding proteins, resulting in the formation of RNA granules, which are then transported within the cytoplasm along the cytoskeleton and delivered to their proper subcellular locations, where they can be locally translated. Here we review current microscopy methods that have been developed to visualize RNA granule formation, transport and translation at the single cell level with a special emphasis on the MS2 and SunTag systems. They include the labeling of mRNAs and RNA-binding proteins in living cells or even the detection of newly synthesized proteins in situ. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:177 / 185
页数:9
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