Inducible Control of mRNA Transport Using Reprogrammable RNA-Binding Proteins

被引:9
|
作者
Abil, Zhanar [1 ]
Gumy, Laura F. [2 ]
Zhao, Huimin [1 ,3 ,4 ]
Hoogenraad, Casper C. [2 ]
机构
[1] Univ Illinois, Dept Biochem, 600 South Mathews Ave, Urbana, IL 61801 USA
[2] Univ Utrecht, Fac Sci, Dept Biol, Cell Biol, Padualaan 8, NL-3584 CH Utrecht, Netherlands
[3] Univ Illinois, Dept Chem & Biomol Engn, Dept Bioengn, Dept Chem, 600 South Mathews Ave, Urbana, IL 61801 USA
[4] Univ Illinois, Inst Genom Biol, 600 South Mathews Ave, Urbana, IL 61801 USA
来源
ACS SYNTHETIC BIOLOGY | 2017年 / 6卷 / 06期
关键词
mRNA transport; kincsin; dynein; RNA-binding proteins (RBP); Pumilio and fem3 mRNA-binding factor (PUF); PUMILIO-HOMOLOGY DOMAIN; PUF PROTEINS; LOCALIZATION; RECOGNITION; SYSTEM; TRAFFICKING; CODE;
D O I
10.1021/acssynbio.7b00025
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Localization of mRNA is important in a number of cellular processes such as embryogenesis, cellular motility, polarity, and a variety of neurological processes. A synthetic device that controls cellular mRNA localization would facilitate investigations on the significance of mRNA localization in cellular function and allow an additional level of controlling gene expression. In this work, we developed the PUF (Pumilio and FBF homology domain)-assisted localization of RNA (PULR) system, which utilizes a eukaryotic cell's cytoskeletal transport machinery to reposition mRNA within a cell. Depending on the cellular motor used, we show ligand-dependent transport of mRNA toward either pole of the microtubular network of cultured cells. In addition, implementation of the reprogrammable PUF domain allowed the transport of untagged endogenous mRNA in primary neurons.
引用
收藏
页码:950 / 956
页数:7
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