Lee Nara, Yario Therese A, Gao Jessica S, Steitz Joan A
Department of Molecular Biophysics and Biochemistry, Yale University School of Medicine, New Haven, CT 06536;
Department of Molecular Biophysics and Biochemistry, Yale University School of Medicine, New Haven, CT 06536; Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, CT 06536
Proc Natl Acad Sci U S A. 2016 Mar 22;113(12):3221-6. doi: 10.1073/pnas.1601773113. Epub 2016 Mar 7.
Epstein-Barr virus (EBV) produces a highly abundant noncoding RNA called EBV-encoded RNA 2 (EBER2) that interacts indirectly with the host transcription factor paired box protein 5 (PAX5) to regulate viral latent membrane protein 1/2 (LMP1/2) gene expression as well as EBV lytic replication. To identify intermediary proteins, we isolated EBER2-PAX5-containing complexes and analyzed the protein components by mass spectrometry. The top candidates include three host proteins splicing factor proline and glutamine rich (SFPQ), non-POU domain-containing octamer-binding protein (NONO), and RNA binding motif protein 14 (RBM14), all reported to be components of nuclear bodies called paraspeckles. In vivo RNA-protein crosslinking indicates that SFPQ and RBM14 contact EBER2 directly. Binding studies using recombinant proteins demonstrate that SFPQ and NONO associate with PAX5, potentially bridging its interaction with EBER2. Similar to EBER2 or PAX5 depletion, knockdown of any of the three host RNA-binding proteins results in the up-regulation of viral LMP2A mRNA levels, supporting a physiologically relevant interaction of these newly identified factors with EBER2 and PAX5. Identification of these EBER2-interacting proteins enables the search for cellular noncoding RNAs that regulate host gene expression in a manner similar to EBER2.
爱泼斯坦-巴尔病毒(EBV)产生一种高度丰富的非编码RNA,称为EBV编码RNA 2(EBER2),它与宿主转录因子配对盒蛋白5(PAX5)间接相互作用,以调节病毒潜伏膜蛋白1/2(LMP1/2)基因的表达以及EBV的裂解复制。为了鉴定中间蛋白,我们分离了含有EBER2-PAX5的复合物,并通过质谱分析了蛋白质成分。最有可能的候选蛋白包括三种宿主蛋白:富含脯氨酸和谷氨酰胺的剪接因子(SFPQ)、含非POU结构域的八聚体结合蛋白(NONO)和RNA结合基序蛋白14(RBM14),所有这些蛋白都被报道是称为副斑点的核小体的组成成分。体内RNA-蛋白质交联表明SFPQ和RBM14直接与EBER2接触。使用重组蛋白进行的结合研究表明,SFPQ和NONO与PAX5结合,可能会桥接其与EBER2的相互作用。与EBER2或PAX5缺失类似,三种宿主RNA结合蛋白中的任何一种被敲低都会导致病毒LMP2A mRNA水平上调,这支持了这些新鉴定的因子与EBER2和PAX5在生理上相关的相互作用。鉴定这些与EBER2相互作用的蛋白有助于寻找以类似于EBER2的方式调节宿主基因表达的细胞非编码RNA。