作者
Xichen Bao,Xiangpeng Guo,Menghui Yin,Muqddas Tariq,Yiwei Lai,Shahzina Kanwal,Jiajian Zhou,Na Li,Yuan Lv,Carlos Pulido-Quetglas,Xiwei Wang,Lu Ji,Muhammad Jawad Khan,Zhu Xihua,Zhiwei Luo,Changwei Shao,Do‐Hwan Lim,Xiao Liu,Nan Li,Wei Wang,Minghui He,Yu-Lin Liu,Carl Ward,Tong Wang,Gong Zhang,Dongye Wang,Jianhua Yang,Yiwen Chen,Chaolin Zhang,Ralf Jauch,Yun‐Gui Yang,Yangming Wang,Baoming Qin,Minna‐Liisa Änkö,Andrew P. Hutchins,Hao Sun,Huating Wang,Xiang‐Dong Fu,Biliang Zhang,Miguel A. Esteban
摘要
We combine the labeling of newly transcribed RNAs with 5-ethynyluridine with the characterization of bound proteins. This approach, named capture of the newly transcribed RNA interactome using click chemistry (RICK), systematically captures proteins bound to a wide range of RNAs, including nascent RNAs and traditionally neglected nonpolyadenylated RNAs. RICK has identified mitotic regulators amongst other novel RNA-binding proteins with preferential affinity for nonpolyadenylated RNAs, revealed a link between metabolic enzymes/factors and nascent RNAs, and expanded the known RNA-bound proteome of mouse embryonic stem cells. RICK will facilitate an in-depth interrogation of the total RNA-bound proteome in different cells and systems.