Borgeson Claudia D, Samson Marie-Laure
Department of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, NE 68198-4525, USA.
Nucleic Acids Res. 2005 Nov 10;33(19):6372-83. doi: 10.1093/nar/gki942. Print 2005.
The product of the Drosophila embryonic lethal abnormal visual system is a conserved protein (ELAV) necessary for normal neuronal differentiation and maintenance. It possesses three RNA-binding domains and is involved in the regulation of RNA metabolism. The long elav 3'-untranslated region (3'-UTR) is necessary for autoregulation. We used RNA-binding assays and in vitro selection to identify the ELAV best binding site in the elav 3'-UTR. This site resembles ELAV-binding sites identified previously in heterologous targets, both for its nucleotide sequence and its significant affinity for ELAV (K(d) 40 nM). This finding supports our model that elav autoregulation depends upon direct interaction between ELAV and elav RNA. We narrowed down the best binding site to a 20 nt long sequence A(U5)A(U3)G(U2)A(U6) in an alternative 3' exon. We propose and test a model in which the regulated use of this alternative 3' exon is involved in normal elav regulation. Found in NEurons (FNE), another neuronal RNA-binding protein paralogous to ELAV, also binds this site. These observations provide a molecular basis for the in vivo interactions reported previously between elav and fne.
果蝇胚胎致死异常视觉系统的产物是一种保守蛋白(ELAV),对于正常神经元的分化和维持是必需的。它具有三个RNA结合结构域,并参与RNA代谢的调控。长的elav 3'非翻译区(3'-UTR)对于自身调节是必需的。我们使用RNA结合分析和体外筛选来鉴定elav 3'-UTR中ELAV的最佳结合位点。该位点在核苷酸序列及其对ELAV的显著亲和力(K(d) 40 nM)方面类似于先前在异源靶标中鉴定的ELAV结合位点。这一发现支持了我们的模型,即elav自身调节依赖于ELAV与elav RNA之间的直接相互作用。我们将最佳结合位点缩小到一个20 nt长的序列A(U5)A(U3)G(U2)A(U6),位于一个可变的3'外显子中。我们提出并测试了一个模型,其中该可变3'外显子的调控使用参与了正常的elav调节。在神经元中发现(FNE),另一种与ELAV同源的神经元RNA结合蛋白,也结合该位点。这些观察结果为先前报道的elav与fne之间的体内相互作用提供了分子基础。