Department of Biological and Molecular Sciences, George Fox University, Newberg, OR 97132, USA.
Knight Cardiovascular Institute, Oregon Health & Science University, Portland, OR 97239, USA.
Int J Mol Sci. 2021 Jan 16;22(2):863. doi: 10.3390/ijms22020863.
The Kv11.1 voltage-gated potassium channel, encoded by the KCNH2 gene, conducts the rapidly activating delayed rectifier current in the heart. KCNH2 pre-mRNA undergoes alternative polyadenylation to generate two C-terminal Kv11.1 isoforms in the heart. Utilization of a poly(A) signal in exon 15 produces the full-length, functional Kv11.1a isoform, while intron 9 polyadenylation generates the C-terminally truncated, nonfunctional Kv11.1a-USO isoform. The relative expression of Kv11.1a and Kv11.1a-USO isoforms plays an important role in the regulation of Kv11.1 channel function. In this study, we tested the hypothesis that the RNA polyadenylate binding protein nuclear 1 (PABPN1) interacts with a unique 22 nt adenosine stretch adjacent to the intron 9 poly(A) signal and regulates KCNH2 pre-mRNA alternative polyadenylation and the relative expression of Kv11.1a C-terminal isoforms. We showed that PABPN1 inhibited intron 9 poly(A) activity using luciferase reporter assays, tandem poly(A) reporter assays, and RNA pulldown assays. We also showed that PABPN1 increased the relative expression level of the functional Kv11.1a isoform using RNase protection assays, immunoblot analyses, and patch clamp recordings. Our present findings suggest a novel role for the RNA-binding protein PABPN1 in the regulation of functional and nonfunctional Kv11.1 isoform expression.
Kv11.1 电压门控钾通道由 KCNH2 基因编码,在心内传导快速激活延迟整流电流。KCNH2 前体 mRNA 通过可变多聚腺苷酸化生成心脏内两种 C 端 Kv11.1 同工型。利用外显子 15 中的多聚 A 信号产生全长功能性 Kv11.1a 同工型,而内含子 9 多聚腺苷酸化产生 C 端截断的、无功能的 Kv11.1a-USO 同工型。Kv11.1a 和 Kv11.1a-USO 同工型的相对表达在 Kv11.1 通道功能的调节中起着重要作用。在这项研究中,我们检验了以下假设:RNA 多聚腺苷酸结合蛋白核 1(PABPN1)与内含子 9 多聚 A 信号旁独特的 22 个核苷酸腺苷序列相互作用,调节 KCNH2 前体 mRNA 的可变多聚腺苷酸化和 Kv11.1a C 端同工型的相对表达。我们表明 PABPN1 通过荧光素酶报告基因检测、串联多聚 A 报告基因检测和 RNA 下拉实验抑制内含子 9 多聚 A 活性。我们还表明,PABPN1 通过 RNase 保护实验、免疫印迹分析和膜片钳记录增加功能性 Kv11.1a 同工型的相对表达水平。我们目前的研究结果表明,RNA 结合蛋白 PABPN1 在功能性和非功能性 Kv11.1 同工型表达的调节中发挥了新的作用。