Published February 16, 2024 | Version v1
Journal article Open

Engineered RNA-binding Proteins: Studying and Controlling RNA Regulation

  • 1. University of Chicago

Description

The complexity of eukaryotic organisms is intricately tied to transcriptome-level processes, notably alternative splicing and the precise modulation of gene expression through a sophisticated interplay involving RNA-binding protein (RBP) networks and their RNA targets. Recent advances in our understanding of the molecular pathways responsible for this control have paved the way for the development of tools capable of steering and managing RNA regulation and gene expression. The fusion between a rapidly developing understanding of endogenous RNA regulation and the burgeoning capabilities of CRISPR-Cas and other programmable RBP platforms has given rise to an exciting frontier in engineered RNA regulators. This review offers an overview of the existing toolkit for constructing synthetic RNA regulators using programmable RBPs and effector domains, capable of altering RNA sequence composition or fate, and explores their diverse applications in both basic research and therapeutic contexts.

Data availability

Data sharing is not applicable to this article as no new data were created or analyzed in this study.

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Additional details

Identifiers

DOI
10.1002/ijch.202300169
Other
oai:uchicago.tind.io:11105

Funding

National Institute of Biomedical Imaging and Bioengineering
R01 EB035016
The G. Harold and Leila Y. Mathers Charitable Foundation
National Science Foundation
Graduate Research Fellowship

UChicago Information

Division(s)
Physical Sciences Division
Department(s)
Chemistry