Department of Laboratory Medicine, Lund University, BMC-B13, 221 84, Lund, Sweden.
China Institute of Sport and Health Sciences, Beijing Sport University, Haidian District, Beijing, People's Republic of China.
Arch Virol. 2022 Feb;167(2):563-570. doi: 10.1007/s00705-021-05317-2. Epub 2021 Dec 3.
We have determined the effect of seven serine- and arginine-rich (SR) proteins and 15 heterogenous nuclear ribonucleoproteins (hnRNPs) on human papillomavirus type 16 (HPV16) late gene expression. Of the seven SR proteins analyzed here, SRSF1, SRSF3, and SRSF9 induced HPV16 late gene expression, and five of the SR proteins affected HPV16 L1 mRNA splicing. Of the 15 hnRNP proteins analyzed here, hnRNP A2, hnRNP F, and hnRNP H efficiently induced HPV16 late gene expression, and all of the hnRNPs affected HPV16 L1 mRNA levels or mRNA splicing. Thus, the majority of SR proteins and hnRNPs have the potential to regulate HPV16 L1 mRNA splicing. Strict control of the expression of the immunogenic L1 and L2 capsid proteins may contribute to the ability of HPV16 to cause persistence.
我们已经确定了七种丝氨酸-精氨酸丰富(SR)蛋白和 15 种异质核核糖核蛋白(hnRNP)对人乳头瘤病毒 16 型(HPV16)晚期基因表达的影响。在分析的七种 SR 蛋白中,SRSF1、SRSF3 和 SRSF9 诱导 HPV16 晚期基因表达,其中五种 SR 蛋白影响 HPV16 L1 mRNA 剪接。在分析的 15 种 hnRNP 蛋白中,hnRNP A2、hnRNP F 和 hnRNP H 有效地诱导 HPV16 晚期基因表达,所有的 hnRNP 都影响 HPV16 L1 mRNA 水平或 mRNA 剪接。因此,大多数 SR 蛋白和 hnRNP 具有调节 HPV16 L1 mRNA 剪接的潜力。对免疫原性 L1 和 L2 衣壳蛋白表达的严格控制可能有助于 HPV16 持续存在的能力。