Benhalevy Daniel, Gupta Sanjay K, Danan Charles H, Ghosal Suman, Sun Hong-Wei, Kazemier Hinke G, Paeschke Katrin, Hafner Markus, Juranek Stefan A
Laboratory of Muscle Stem Cells and Gene Regulation, National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, MD 20892, USA.
Department of Biochemistry, Biocenter, University of Würzburg, Am Hubland, 97074 Würzburg, Germany.
Cell Rep. 2017 Mar 21;18(12):2979-2990. doi: 10.1016/j.celrep.2017.02.080.
The CCHC-type zinc finger nucleic acid-binding protein (CNBP/ZNF9) is conserved in eukaryotes and is essential for embryonic development in mammals. It has been implicated in transcriptional, as well as post-transcriptional, gene regulation; however, its nucleic acid ligands and molecular function remain elusive. Here, we use multiple systems-wide approaches to identify CNBP targets and function. We used photoactivatable ribonucleoside-enhanced crosslinking and immunoprecipitation (PAR-CLIP) to identify 8,420 CNBP binding sites on 4,178 mRNAs. CNBP preferentially bound G-rich elements in the target mRNA coding sequences, most of which were previously found to form G-quadruplex and other stable structures in vitro. Functional analyses, including RNA sequencing, ribosome profiling, and quantitative mass spectrometry, revealed that CNBP binding did not influence target mRNA abundance but rather increased their translational efficiency. Considering that CNBP binding prevented G-quadruplex structure formation in vitro, we hypothesize that CNBP is supporting translation by resolving stable structures on mRNAs.
CCHC型锌指核酸结合蛋白(CNBP/ZNF9)在真核生物中保守,对哺乳动物胚胎发育至关重要。它涉及转录以及转录后基因调控;然而,其核酸配体和分子功能仍不清楚。在这里,我们使用多种全系统方法来鉴定CNBP的靶点和功能。我们使用光活化核糖核苷增强交联和免疫沉淀(PAR-CLIP)来鉴定4178个mRNA上的8420个CNBP结合位点。CNBP优先结合靶mRNA编码序列中的富含G的元件,其中大多数先前已发现可在体外形成G-四链体和其他稳定结构。功能分析,包括RNA测序、核糖体分析和定量质谱,表明CNBP结合不影响靶mRNA丰度,而是提高其翻译效率。鉴于CNBP结合在体外可防止G-四链体结构形成,我们推测CNBP通过解析mRNA上的稳定结构来支持翻译。