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G-quadruplexes offer a conserved structural motif for NONO recruitment to NEAT1 architectural lncRNA

机译:G-四链体为NOEAT募集NEAT1建筑lncRNA提供了保守的结构基序

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摘要

The long non-coding RNA NEAT1 serves as a scaffold for the assembly of paraspeckles, membraneless nuclear organelles involved in gene regulation. Paraspeckle assembly requires NEAT1 recruitment of the RNA-binding protein NONO, however the NEAT1 elements responsible for recruitment are unknown. Herein we present evidence that previously unrecognized structural features of NEAT1 serve an important role in these interactions. Led by the initial observation that NONO preferentially binds the G-quadruplex conformation of G-rich repeat RNA, we find that G-quadruplex motifs are abundant and conserved features of NEAT1. Furthermore, we determine that NONO binds NEAT1 G-quadruplexes with structural specificity and provide evidence that G-quadruplex motifs mediate NONO-NEAT1 association, with NONO binding sites on NEAT1 corresponding largely to G-quadruplex motifs, and treatment with a G-quadruplex-disrupting small molecule causing dissociation of native NONO-NEAT1 complexes. Together, these findings position G-quadruplexes as a primary candidate for the NONO-recruiting elements of NEAT1 and provide a framework for further investigation into the role of G-quadruplexes in paraspeckle formation and function.
机译:长长的非编码RNA NEAT1充当了一个支架,用于组装参与基因调控的散斑,无膜核细胞器。散斑组装需要NEAT1募集RNA结合蛋白NONO,但是负责募集的NEAT1元件尚不清楚。在本文中,我们提供证据表明,以前无法识别的NEAT1结构特征在这些相互作用中起着重要的作用。最初观察到NONO优先结合富含G的重复RNA的G-四链体构象,我们发现G-四链体基序丰富且保守NEAT1的特征。此外,我们确定NONO以结构特异性结合NEAT1 G-四链体,并提供证据表明G-四链体基序介导NONO-NEAT1关联,NEAT1上的NONO结合位点主要对应于G-四链体基序,并用G-四链体-进行治疗。破坏小分子,导致天然NONO-NEAT1复合物解离。总之,这些发现将G-四链体定位为NEAT1的NONO募集元件的主要候选者,并为进一步研究G-四链体在散斑形成和功能中的作用提供了框架。

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