학술논문

Large-scale tethered function assays identify factors that regulate mRNA stability and translation
Document Type
article
Source
Nature Structural & Molecular Biology. 27(10)
Subject
Biochemistry and Cell Biology
Biological Sciences
Genetics
Underpinning research
1.1 Normal biological development and functioning
Generic health relevance
3' Untranslated Regions
Binding Sites
CRISPR-Cas Systems
Carrier Proteins
Cell Line
Humans
Luciferases
Open Reading Frames
Polyribosomes
Protein Biosynthesis
RNA Stability
RNA-Binding Proteins
Recombinant Proteins
Ultraviolet Rays
Chemical Sciences
Medical and Health Sciences
Biophysics
Developmental Biology
Biological sciences
Biomedical and clinical sciences
Chemical sciences
Language
Abstract
The molecular functions of the majority of RNA-binding proteins (RBPs) remain unclear, highlighting a major bottleneck to a full understanding of gene expression regulation. Here, we develop a plasmid resource of 690 human RBPs that we subject to luciferase-based 3'-untranslated-region tethered function assays to pinpoint RBPs that regulate RNA stability or translation. Enhanced UV-cross-linking and immunoprecipitation of these RBPs identifies thousands of endogenous mRNA targets that respond to changes in RBP level, recapitulating effects observed in tethered function assays. Among these RBPs, the ubiquitin-associated protein 2-like (UBAP2L) protein interacts with RNA via its RGG domain and cross-links to mRNA and rRNA. Fusion of UBAP2L to RNA-targeting CRISPR-Cas9 demonstrates programmable translational enhancement. Polysome profiling indicates that UBAP2L promotes translation of target mRNAs, particularly global regulators of translation. Our tethering survey allows rapid assignment of the molecular activity of proteins, such as UBAP2L, to specific steps of mRNA metabolism.