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Targeted translational regulation using the PUF protein family scaffold.

Authors :
Cooke, Amy
Prigge, Andrew
Opperman, Laura
Wickens, Marvin
Source :
Proceedings of the National Academy of Sciences of the United States of America. 9/20/2011, Vol. 108 Issue 38, p15870-15875. 6p.
Publication Year :
2011

Abstract

Regulatory complexes formed on mRNAs control translation, stability, and localization. These complexes possess two activities: one that binds RNA and another—the effector—that elicits a biological function. The Pumilio and FBF (PUF) protein family of RNA binding proteins provides a versatile scaffold to design and select proteins with new specificities. Here, the PUF scaffold is used to target translational activation and repression of specific mRNAs, and to induce specific poly(A) addition and removal. To do so, we linked PUF scaffold proteins to a tyanslational activator, GLDZ. or a translational repressor,CAF1. The chimeric proteins activate or repress the targeted mRNA5 in Xenopus oocytes, and elicit poly(A) addition or removal. The magnitude of translational control relates directly to the affinity of the RNA-protein complex over a 100-fold range of Kd. The chimeric proteins act on both reporter and endogenous mRNAs: an mRNA that normally is deadenylated during oocyte maturation instead receives poly(A) in the presence of an appropriate chimera. The PUF-effector strategy enables the design of proteins that affect translation and stability of specific mRNAs in vivo. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00278424
Volume :
108
Issue :
38
Database :
Academic Search Index
Journal :
Proceedings of the National Academy of Sciences of the United States of America
Publication Type :
Academic Journal
Accession number :
66701979
Full Text :
https://doi.org/10.1073/pnas.1105151108