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从 HPV16 晚期 mRNA 中剪接的 SD880 到 SA2709 的 HPV16 E2 蛋白的高效生产。

Efficient production of HPV16 E2 protein from HPV16 late mRNAs spliced from SD880 to SA2709.

机构信息

Department of Laboratory Medicine, Lund University, BMC-B13, 221 84, Lund, Sweden.

Department of Laboratory Medicine, Lund University, BMC-B13, 221 84, Lund, Sweden; China Institute of Sport and Health Sciences, Beijing Sport University, Xinxi Road 48, Haidian District, 100084, Beijing, China.

出版信息

Virus Res. 2020 Aug;285:198004. doi: 10.1016/j.virusres.2020.198004. Epub 2020 May 5.

Abstract

Human papillomaviruses (HPVs) produce a large number of alternatively spliced mRNAs, including a number of differently spliced mRNAs with the potential to produce E2 protein. To identify the alternatively spliced HPV16 mRNA with the highest ability to produce E2 protein, we have generated E2 cDNA expression plasmids representing the most common, alternatively spliced E2 mRNAs, and assessed their translational potential. Our results revealed that an mRNA initiated at the HPV16 late promoter p670 and spliced from the HPV16 5'-splice site SD880 to the HPV16 3'-splice site SA2709, located immediately upstream of the E2 ATG, produced higher levels of E2 than any of the other alternatively spliced, E2-encoding mRNAs. Utilization of a known, alternative 3'-splice site located upstream of the E2 ATG named SA2582, generated mRNAs with lower ability to produce E2 than mRNAs spliced to SA2709. Finally, analysis of HPV16 mRNA splicing demonstrated that SA2709 was more efficiently spliced to the upstream 5'-splice site SD880 than to the upstream 5'-splice site SD226. In conclusion, the HPV16 mRNA with the greatest ability to produce E2 protein is generated from the HPV16 late promoter and is spliced between HPV16 5'-splice site SD880 and HPV16 3'-splice site SA2709.

摘要

人乳头瘤病毒 (HPV) 产生大量的选择性剪接 mRNA,包括许多具有产生 E2 蛋白潜力的不同剪接 mRNA。为了鉴定具有最高产生 E2 蛋白能力的 HPV16 选择性剪接 mRNA,我们生成了代表最常见的 HPV16 剪接 E2 mRNA 的 E2 cDNA 表达质粒,并评估了它们的翻译潜力。我们的结果表明,从 HPV16 晚期启动子 p670 起始并从 HPV16 5'-剪接位点 SD880 剪接到 HPV16 3'-剪接位点 SA2709 的 HPV16 mRNA,该位点位于 E2 ATG 上游,产生的 E2 水平高于任何其他剪接的、编码 E2 的 mRNA。利用位于 E2 ATG 上游的已知替代 3'-剪接位点 SA2582,产生的 E2 蛋白比剪接到 SA2709 的 mRNA 产生的 E2 蛋白能力更低。最后,对 HPV16 mRNA 剪接的分析表明,SA2709 比上游 5'-剪接位点 SD226 更有效地剪接到上游 5'-剪接位点 SD880。总之,具有最强产生 E2 蛋白能力的 HPV16 mRNA 是从 HPV16 晚期启动子产生的,并在 HPV16 5'-剪接位点 SD880 和 HPV16 3'-剪接位点 SA2709 之间剪接。

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