Ishizuka Akira, Hasegawa Yuko, Ishida Kentaro, Yanaka Kaori, Nakagawa Shinichi
RNA Biology Laboratory, RIKEN, 2-1 Hirosawa, Wako, Saitama, 351-0198, Japan.
Genes Cells. 2014 Sep;19(9):704-21. doi: 10.1111/gtc.12169.
Gomafu/MIAT/Rncr2 is a long noncoding RNA that has been proposed to control retinal cell specification, stem cell differentiation and alternative splicing of schizophrenia-related genes. However, how Gomafu controls these biological processes at the molecular level has remained largely unknown. In this study, we identified the RNA-binding protein Celf3 as a novel Gomafu-associating protein. Knockdown of Celf3 led to the down-regulation of Gomafu, and cross-link RNA precipitation analysis confirmed specific binding between Celf3 and Gomafu. In the neuroblastoma cell line Neuro2A, Celf3 formed novel nuclear bodies (named CS bodies) that colocalized with SF1, another Gomafu-binding protein. Gomafu, however, was not enriched in the CS bodies; instead, it formed distinct nuclear bodies in separate regions in the nucleus. These observations suggest that Gomafu indirectly modulates the function of the splicing factors SF1 and Celf3 by sequestering these proteins into separate nuclear bodies.
Gomafu/MIAT/Rncr2是一种长链非编码RNA,有人提出它可控制视网膜细胞特化、干细胞分化以及精神分裂症相关基因的可变剪接。然而,Gomafu如何在分子水平上控制这些生物学过程在很大程度上仍不清楚。在本研究中,我们鉴定出RNA结合蛋白Celf3是一种新的与Gomafu相关的蛋白。敲低Celf3导致Gomafu下调,交联RNA沉淀分析证实了Celf3与Gomafu之间的特异性结合。在神经母细胞瘤细胞系Neuro2A中,Celf3形成了与另一种Gomafu结合蛋白SF1共定位的新型核体(称为CS体)。然而,Gomafu在CS体中并不富集;相反,它在细胞核的不同区域形成了不同的核体。这些观察结果表明,Gomafu通过将这些蛋白隔离到不同的核体中来间接调节剪接因子SF1和Celf3的功能。