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A universal strategy for regulating mRNA translation in prokaryotic and eukaryotic cells.


ABSTRACT: We describe a simple strategy to control mRNA translation in both prokaryotic and eukaryotic cells which relies on a unique protein-RNA interaction. Specifically, we used the Pumilio/FBF (PUF) protein to repress translation by binding in between the ribosome binding site (RBS) and the start codon (in Escherichia coli), or by binding to the 5' untranslated region of target mRNAs (in mammalian cells). The design principle is straightforward, the extent of translational repression can be tuned and the regulator is genetically encoded, enabling the construction of artificial signal cascades. We demonstrate that this approach can also be used to regulate polycistronic mRNAs; such regulation has rarely been achieved in previous reports. Since the regulator used in this study is a modular RNA-binding protein, which can be engineered to target different 8-nucleotide RNA sequences, our strategy could be used in the future to target endogenous mRNAs for regulating metabolic flows and signaling pathways in both prokaryotic and eukaryotic cells.

SUBMITTER: Cao J 

PROVIDER: S-EPMC4417184 | biostudies-literature | 2015 Apr

REPOSITORIES: biostudies-literature

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A universal strategy for regulating mRNA translation in prokaryotic and eukaryotic cells.

Cao Jicong J   Arha Manish M   Sudrik Chaitanya C   Mukherjee Abhirup A   Wu Xia X   Kane Ravi S RS  

Nucleic acids research 20150406 8


We describe a simple strategy to control mRNA translation in both prokaryotic and eukaryotic cells which relies on a unique protein-RNA interaction. Specifically, we used the Pumilio/FBF (PUF) protein to repress translation by binding in between the ribosome binding site (RBS) and the start codon (in Escherichia coli), or by binding to the 5' untranslated region of target mRNAs (in mammalian cells). The design principle is straightforward, the extent of translational repression can be tuned and  ...[more]

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