Targeted RNA condensation in living cells via genetically encodable triplet repeat tags

Author:

Xue Zhaolin1,Ren Kewei12,Wu Rigumula1,Sun Zhining1,Zheng Ru1,Tian Qian1,Ali Ahsan Ausaf1,Mi Lan1,You Mingxu13ORCID

Affiliation:

1. Department of Chemistry, University of Massachusetts , Amherst , MA  01003 , USA

2. School of Chemistry and Chemical Engineering, Nanjing University of Science and Technology , Nanjing  210094 , China

3. Molecular and Cellular Biology Program, University of Massachusetts , Amherst , MA  01003 , USA

Abstract

Abstract Living systems contain various membraneless organelles that segregate proteins and RNAs via liquid–liquid phase separation. Inspired by nature, many protein-based synthetic compartments have been engineered in vitro and in living cells. Here, we introduce a genetically encoded CAG-repeat RNA tag to reprogram cellular condensate formation and recruit various non-phase-transition RNAs for cellular modulation. With the help of fluorogenic RNA aptamers, we have systematically studied the formation dynamics, spatial distributions, sizes and densities of these cellular RNA condensates. The cis- and trans-regulation functions of these CAG-repeat tags in cellular RNA localization, life time, RNA–protein interactions and gene expression have also been investigated. Considering the importance of RNA condensation in health and disease, we expect that these genetically encodable modular and self-assembled tags can be widely used for chemical biology and synthetic biology studies.

Funder

NSF

Camille Dreyfus Teacher-Scholar

NIH

Publisher

Oxford University Press (OUP)

Subject

Genetics

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