category
NAR
date
Feb 27, 2026
slug
status
Published
summary
创新性开发了不稳定双顺反子荧光蛋白报告系统(dBFPR)提升APA检测灵敏度,并整合CRISPR/Cas9与流式细胞术建立高通量筛选平台,发现PABPN1作为APA调控网络的核心枢纽蛋白
tags
基因编辑
合成生物学
蛋白质组学
type
Post
📄 原文题目
CRISPR/Cas9 screening with destabilized bicistronic fluorescent protein reporter revealed PABPN1 as a hub of regulators for alternative polyadenylation
🔗 原文链接
💡 AI 核心解读
创新性开发了不稳定双顺反子荧光蛋白报告系统(dBFPR)提升APA检测灵敏度,并整合CRISPR/Cas9与流式细胞术建立高通量筛选平台,发现PABPN1作为APA调控网络的核心枢纽蛋白
📝 英文原版摘要
<span class="paragraphSection"><div class="boxTitle">Abstract</div>Alternative polyadenylation (APA) is intricately intertwined with diverse biological processes. Efficient approaches for screening the regulatory factors of specific APA events are essential to elucidate their regulation mechanisms. Here, we first engineered a destabilized bicistronic fluorescent protein reporter (dBFPR) to enhance the sensitivity of APA detection. Then, we developed a robust high-throughput screening platform for APA regulators by integrating CRISPR/Cas9, dBFPR, and fluorescence-activated cell sorting. With this method, we successfully screened the library of RNA binding proteins and found that PTBP1, ELAVL1, and DDX3X play significant roles in regulating APA and promoting cell proliferation through interaction with PABPN1, suggesting that PABPN1 is an important hub for APA regulation.</span>
- 作者:NotionNext
- 链接:https://tangly1024.com/article/31448bd6-1f96-812e-b957-f4e6d34edea2
- 声明:本文采用 CC BY-NC-SA 4.0 许可协议,转载请注明出处。
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