CellREADR: An ADAR-based RNA sensor-actuator device.

4区 生物学 Q3 Biochemistry, Genetics and Molecular Biology
Methods in enzymology Pub Date : 2025-01-01 Epub Date: 2025-01-10 DOI:10.1016/bs.mie.2024.11.027
Xiaolu Yang, Kehali Woldemichael, Xiao Guo, Shengli Zhao, Yongjun Qian, Z Josh Huang
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引用次数: 0

Abstract

RNAs are central mediators of genetic information flow and gene regulation that underlie diverse cell types and cell states across species. Thus, methods that can sense and respond to RNA profiles in living cells will have broad applications in biology and medicine. CellREADR - Cell access through RNA sensing by Endogenous ADAR (adenosine deaminase acting on RNA), is a programmable RNA sensor-actuator technology that couples the detection of a cell-defining RNA to the translation of an effector protein to monitor and manipulate the cell. The CellREADR RNA device consists of a 5' sensor region complementary to a cellular RNA and a 3' protein payload coding region. Payload translation is gated by the removal of a STOP codon in the sensor region upon base pairing with the cognate cellular RNA through an ADAR-mediated A-to-I editing mechanism ubiquitous to metazoan cells. CellREADR thus represents a new generation of programmable RNA device for monitoring and manipulating animal cells in ways that are simple, versatile, and generalizable across tissues and species. Here, we describe a detailed procedure for implementing CellREADR experiments in cell culture systems and in animals. The procedure includes sensor and payload design, cloning, validation and characterization in mammalian cell cultures. The in vivo protocol focuses on AAV-based delivery of CellREADR through expression vectors using brain tissue as an example. We describe current best practices and various experimental controls.

CellREADR:一种基于adar的RNA传感器致动器设备。
rna是遗传信息流和基因调控的中心介质,是跨物种不同细胞类型和细胞状态的基础。因此,能够感知和响应活细胞RNA谱的方法将在生物学和医学上有广泛的应用。CellREADR -通过内源性ADAR(腺苷脱氨酶作用于RNA)的RNA传感进入细胞,是一种可编程的RNA传感器-致动器技术,将细胞定义RNA的检测与效应蛋白的翻译结合起来,以监测和操纵细胞。CellREADR RNA装置由一个与细胞RNA互补的5‘传感器区和一个3’蛋白质有效载荷编码区组成。有效载荷翻译是通过adar介导的a -to- i编辑机制在与同源细胞RNA进行碱基配对时去除传感器区域的STOP密码子来控制的,这种机制在后生动物细胞中普遍存在。因此,CellREADR代表了新一代可编程RNA设备,用于以简单、通用、跨组织和物种的方式监测和操纵动物细胞。在这里,我们描述了在细胞培养系统和动物中实施CellREADR实验的详细程序。程序包括传感器和有效载荷设计,克隆,验证和哺乳动物细胞培养的特性。体内方案的重点是基于aav通过表达载体传递CellREADR,以脑组织为例。我们描述了当前的最佳实践和各种实验控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Methods in enzymology
Methods in enzymology 生物-生化研究方法
CiteScore
2.90
自引率
0.00%
发文量
308
审稿时长
3-6 weeks
期刊介绍: The critically acclaimed laboratory standard for almost 50 years, Methods in Enzymology is one of the most highly respected publications in the field of biochemistry. Each volume is eagerly awaited, frequently consulted, and praised by researchers and reviewers alike. Now with over 500 volumes the series contains much material still relevant today and is truly an essential publication for researchers in all fields of life sciences, including microbiology, biochemistry, cancer research and genetics-just to name a few. Five of the 2013 Nobel Laureates have edited or contributed to volumes of MIE.
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