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Capturing the interactome of newly transcribed RNA.

Xichen BaoXiangpeng GuoMenghui YinMuqddas TariqYiwei LaiShahzina KanwalJiajian ZhouNa LiYuan LvCarlos Pulido-QuetglasXiwei WangLu JiMuhammad J KhanXihua ZhuZhiwei LuoChangwei ShaoDo-Hwan LimXiao LiuNan LiWei WangMinghui HeYu-Lin LiuCarl WardTong WangGong ZhangDongye WangJian-Hua YangYiwen ChenChaolin ZhangRalf JauchYun-Gui YangYangming WangBaoming QinMinna-Liisa AnkoAndrew P HutchinsHao SunHuating WangXiang-Dong FuBiliang ZhangMiguel Angel Esteban
Published in: Nature methods (2018)
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.
Keyphrases
  • embryonic stem cells
  • nucleic acid
  • signaling pathway
  • transcription factor
  • single cell
  • cell death
  • drug discovery