Jang Gwendolyn M, Tanaka Brian S, Gutman George A, Goldin Alan L, Semler Bert L
Department of Microbiology and Molecular Genetics, School of Medicine, University of California, Irvine, CA 92697, USA.
Gene. 2008 Jan 31;408(1-2):133-45. doi: 10.1016/j.gene.2007.10.029. Epub 2007 Nov 6.
We investigated the role of the 3' non-coding region of a mouse voltage-gated potassium channel mRNA (mKv1.4 mRNA) in post-transcriptional regulation of gene expression. In contrast to an earlier report from studies carried out in Xenopus oocytes, we found that 3' non-coding region sequences of mKv1.4 mRNAs did not significantly affect expression of a heterologous reporter RNA in vitro or in mammalian cells/cell lines. Instead, our data revealed a possible role for alternative polyadenylation mediated by distinct determinants approximately 0.2 kb and approximately 1.2 kb downstream of the Kv1.4 coding region. The use of the downstream polyadenylation signal correlated with the synthesis of a larger Kv1.4 mRNA isoform that was more abundantly expressed than the smaller mRNA species, whose expression was regulated by the upstream polyadenylation signal. Our results suggest that the relative strengths of the polyadenylation signals are major determinants of overall Kv1.4 mRNA abundance in cells.
我们研究了小鼠电压门控钾通道mRNA(mKv1.4 mRNA)的3'非编码区在基因表达转录后调控中的作用。与之前在非洲爪蟾卵母细胞中进行的研究报告相反,我们发现mKv1.4 mRNA的3'非编码区序列在体外或哺乳动物细胞/细胞系中对异源报告RNA的表达没有显著影响。相反,我们的数据揭示了在Kv1.4编码区下游约0.2 kb和约1.2 kb处由不同决定因素介导的可变聚腺苷酸化可能发挥的作用。下游聚腺苷酸化信号的使用与一种更大的Kv1.4 mRNA异构体的合成相关,该异构体比由上游聚腺苷酸化信号调控表达的较小mRNA种类表达更为丰富。我们的结果表明,聚腺苷酸化信号的相对强度是细胞中Kv1.4 mRNA总体丰度的主要决定因素。