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Inhibition of HPV-16 L1 expression from L1 cDNAs correlates with the presence of hnRNP A1 binding sites in the L1 coding region

机译:从L1 cDNA抑制HPV-16 L1表达与L1编码区中hnRNP A1结合位点的存在有关

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摘要

The human papillomavirus type 16 (HPV-16) L1 capsid protein is very poorly expressed from cDNA expression plasmids transiently transfected into mammalian cells. The results described herein demonstrate that inhibition of HPV-16 L1 expression from L1 cDNAs correlates with the presence of splicing regulatory sequences in the L1 coding region. This inhibitory effect correlates with the binding of hnRNP A1 to the RNA elements. Similar to unutilised splice sites that may retain mRNAs in the nucleus, regulatory splicing RNA elements may also inhibit gene expression in the absence of splicing. The results presented here explain the inefficient expression of HPV-16 L1 protein from the wild type L1 cDNA expression plasmids in mammalian cells. These results may be of general interest since alteration of RNA sequences to prevent unwanted RNA–protein interactions may increase expression of many different genes in transient transfections or after plasmid uptake in DNA vaccination approaches.
机译:人类乳头瘤病毒16型(HPV-16)L1衣壳蛋白从瞬时转染到哺乳动物细胞中的cDNA表达质粒表达非常差。本文所述的结果证明,抑制来自L1 cDNA的HPV-16 L1表达与L1编码区中剪接调控序列的存在有关。该抑制作用与hnRNP A1与RNA元件的结合相关。与可能在细胞核中保留mRNA的未利用的剪接位点相似,在没有剪接的情况下,调节性剪接RNA元件也可能抑制基因表达。此处显示的结果解释了哺乳动物细胞中野生型L1 cDNA表达质粒无法高效表达HPV-16 L1蛋白。这些结果可能是普遍感兴趣的,因为改变RNA序列以防止有害的RNA-蛋白质相互作用可能会增加瞬时转染中或DNA疫苗接种方法中质粒摄取后许多不同基因的表达。

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