Wolford J K, Signs S A
Department of Pharmacology, Northeastern Ohio Universities College of Medicine, Rootstown 44272, USA.
Biochem Biophys Res Commun. 1995 Jun 26;211(3):819-25. doi: 10.1006/bbrc.1995.1885.
Multimeric AUUUA elements in an AU-rich 3'-untranslated region (3'-UTR) have been shown to confer message instability to numerous ephemeral transcripts through the formation of RNA-protein complexes. We show here that the 3'-UTR of VIP mRNA, which contains 3 AUUUA motifs in an AU-rich context, forms specific complexes with cytoplasmic proteins in a concentration-dependent, tissue-specific manner. We also demonstrate that an AU-rich segment of c-fos mRNA can successfully compete with VIP mRNA for binding with cytoplasmic proteins. These studies provide the first evidence for a mechanism by which VIP is post-transcriptionally regulated through specific sequences in its 3'-UTR.
富含AU的3'非翻译区(3'-UTR)中的多聚体AUUUA元件已被证明可通过形成RNA-蛋白质复合物赋予许多短暂转录本信息不稳定性。我们在此表明,VIP mRNA的3'-UTR在富含AU的环境中包含3个AUUUA基序,它以浓度依赖性、组织特异性方式与细胞质蛋白形成特定复合物。我们还证明,c-fos mRNA的富含AU片段可以成功地与VIP mRNA竞争与细胞质蛋白的结合。这些研究为VIP通过其3'-UTR中的特定序列进行转录后调控的机制提供了首个证据。