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Visualization and characterization of RNA-protein interactions in living cells
被引:6
|作者:
Duan, Ningjun
[1
,4
]
Arroyo, Maria
[3
]
Deng, Wen
[1
,2
]
Cardoso, M. Cristina
[3
]
Leonhardt, Heinrich
[1
]
机构:
[1] Ludwig Maximilians Univ Munchen, Dept Biol 2, D-81377 Munich, Germany
[2] Northwest A&F Univ, Coll Vet Med, Yangling 712100, Shaanxi, Peoples R China
[3] Tech Univ Darmstadt, Dept Biol, D-64287 Darmstadt, Germany
[4] Nanjing Med Univ, Dept Oncol, Affiliated Hosp 1, Nanjing 210029, Peoples R China
关键词:
NUCLEAR LAMINA;
CRYSTAL-STRUCTURE;
PUMILIO;
BINDING;
RECOGNITION;
HOTAIR;
EZH2;
PHOSPHORYLATION;
CRISPR-CAS9;
SPECIFICITY;
D O I:
10.1093/nar/gkab614
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
RNA-protein interactions are the structural and functional basis of significant numbers of RNA molecules. RNA-protein interaction assays though, still mainly depend on biochemical tests in vitro. Here, we establish a convenient and reliable RNA fluorescent three-hybrid (rF3H) method to detect/interrogate the interactions between RNAs and proteins in cells. A GFP tagged highly specific RNA trap is constructed to anchor the RNA of interest to an artificial or natural subcellular structure, and RNA-protein interactions can be detected and visualized by the enrichment of RNA binding proteins (RBPs) at these structures. Different RNA trapping systems are developed and detection of RNA-protein complexes at multiple subcellular structures are assayed. With this new toolset, interactions between proteins and mRNA or noncoding RNAs are characterized, including the interaction between a long noncoding RNA and an epigenetic modulator. Our approach provides a flexible and reliable method for the characterization of RNA-protein interactions in living cells. [GRAPHICS] .
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页数:14
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