Department of Biological Sciences, University of South Carolina, Columbia, SC 29208, USA.
Department of Neurosciences, University of New Mexico School of Medicine, Albuquerque, NM 87131, USA.
J Cell Sci. 2017 Nov 1;130(21):3650-3662. doi: 10.1242/jcs.201244. Epub 2017 Sep 4.
HuD protein (also known as ELAVL4) has been shown to stabilize mRNAs with AU-rich elements (ARE) in their 3' untranslated regions (UTRs), including , which has been linked to axon growth. HuD also binds to neuritin () mRNA, whose 3'UTR contains ARE sequences. Although the 3'UTR has been shown to mediate its axonal localization in embryonic hippocampal neurons, it is not active in adult dorsal root ganglion (DRG) neurons. Here, we asked why the 3'UTR is not sufficient to mediate the axonal localization of mRNA in DRG neurons. HuD overexpression increases the ability of the 3'UTR to mediate axonal localizing in DRG neurons. HuD binds directly to the ARE with about a two-fold higher affinity than to the ARE. Although the ARE can displace the from HuD binding, HuD binds to the full 3'UTR of with higher affinity, such that higher levels of are needed to displace the 3'UTR. The 3'UTR can mediate a higher level of axonal localization when endogenous is depleted from DRG neurons. Taken together, our data indicate that endogenous and mRNAs compete for binding to HuD for their axonal localization and activity of the 3'UTR.
HuD 蛋白(也称为 ELAVL4)已被证明可以稳定其 3'非翻译区(UTR)中含有 AU 丰富元件(ARE)的 mRNAs,包括 ,其与轴突生长有关。HuD 还与神经粘蛋白()mRNA 结合,其 3'UTR 包含 ARE 序列。尽管 3'UTR 已被证明介导其在胚胎海马神经元中的轴突定位,但在成年背根神经节(DRG)神经元中它不活跃。在这里,我们想知道为什么 3'UTR 不足以介导 在 DRG 神经元中的轴突定位。HuD 的过表达增加了 3'UTR 介导 DRG 神经元中轴突定位的能力。HuD 直接与 ARE 结合,亲和力比与 ARE 结合高约两倍。尽管 ARE 可以取代 与 HuD 的结合,但 HuD 与 的全长 3'UTR 结合的亲和力更高,因此需要更高水平的 来取代 3'UTR。当 DRG 神经元中耗尽内源性 时,3'UTR 可以介导更高水平的轴突定位。总之,我们的数据表明,内源性 和 mRNAs 竞争与 HuD 结合以实现其轴突定位和 3'UTR 的活性。