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ELAV抑制3'端加工以促进ewg前体mRNA的神经剪接。

ELAV inhibits 3'-end processing to promote neural splicing of ewg pre-mRNA.

作者信息

Soller Matthias, White Kalpana

机构信息

Department of Biology and Volen Center for Complex Systems, Brandeis University, Waltham, Massachusetts 02454, USA.

出版信息

Genes Dev. 2003 Oct 15;17(20):2526-38. doi: 10.1101/gad.1106703. Epub 2003 Oct 1.

Abstract

The embryonic lethal abnormal visual system (ELAV) is a gene-specific regulator of alternative pre-mRNA processing in neurons of Drosophila. Here we define a functional in vivo binding site for ELAV in neurons through the development of a reporter gene system in transgenic animals in combination with in vitro binding assays. ELAV binds to erect wing (ewg) RNA 3' of a polyadenylation site in the terminal intron 6. At this polyadenylation site, ELAV inhibits 3'-end processing in vitro in a dose-dependent and sequence-specific manner, and ELAV binding is necessary in vivo to promote splicing of ewg intron 6. Further, the AAUAAA poly(A) complex recognition sequence, together with ELAV, is required to regulate neural 3' splice site choice in vivo. In addition, the use of segmentally labeled RNA substrates in UV cross-linking assays suggest that ELAV does not inhibit or redirect binding of cleavage factor dCstF64 at the regulated polyadenylation site on ewg RNA. These data indicate that binding of 3'-end processing factors, together with ELAV, can regulate alternative splicing.

摘要

胚胎致死异常视觉系统(ELAV)是果蝇神经元中前体mRNA可变加工的基因特异性调节因子。在此,我们通过在转基因动物中开发报告基因系统并结合体外结合试验,确定了ELAV在神经元中的功能性体内结合位点。ELAV结合于末端内含子6中聚腺苷酸化位点下游的直立翅(ewg)RNA。在这个聚腺苷酸化位点,ELAV在体外以剂量依赖性和序列特异性方式抑制3'末端加工,并且在体内ELAV结合对于促进ewg内含子6的剪接是必需的。此外,AAUAAA聚(A)复合识别序列与ELAV一起,在体内调节神经3'剪接位点选择时是必需的。另外,在紫外线交联试验中使用分段标记的RNA底物表明,ELAV不会抑制或重定向切割因子dCstF64在ewg RNA上受调控的聚腺苷酸化位点的结合。这些数据表明,3'末端加工因子与ELAV的结合可调节可变剪接。

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