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Differences in Transcriptional Activity of Human Papillomavirus Type 6 Molecular Variants in Recurrent Respiratory Papillomatosis

机译:复发性呼吸道乳头状瘤病中人类乳头瘤病毒6型分子变异的转录活性的差异。

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摘要

A significant proportion of recurrent respiratory papillomatosis (RRP) is caused by human papillomavirus type 6 (HPV-6). The long control region (LCR) contains cis-elements for regulation of transcription. Our aim was to characterize LCR HPV-6 variants in RRP cases, compare promoter activity of these isolates and search for cellular transcription factors (TFs) that could explain the differences observed. The complete LCR from 13 RRP was analyzed. Transcriptional activity of 5 variants was compared using luciferase assays. Differences in putative TFs binding sites among variants were revealed using the TRANSFAC database. Chromatin immunoprecipation (CHIP) and luciferase assays were used to evaluate TF binding and impact upon transcription, respectively. Juvenile-onset RRP cases harbored exclusively HPV-6vc related variants, whereas among adult-onset cases HPV-6a variants were more prevalent. The HPV-6vc reference was more transcriptionally active than the HPV-6a reference. Active FOXA1, ELF1 and GATA1 binding sites overlap variable nucleotide positions among isolates and influenced LCR activity. Furthermore, our results support a crucial role for ELF1 on transcriptional downregulation. We identified TFs implicated in the regulation of HPV-6 early gene expression. Many of these factors are mutated in cancer or are putative cancer biomarkers, and must be further studied.
机译:复发性呼吸道乳头状瘤病(RRP)的很大一部分是由6型人乳头瘤病毒(HPV-6)引起的。长控制区(LCR)包含顺式元件,用于调节转录。我们的目的是鉴定RRP病例中的LCR HPV-6变异体,比较这些分离株的启动子活性,并寻找可以解释所观察到差异的细胞转录因子(TF)。分析了来自13 RRP的完整LCR。使用萤光素酶测定法比较了5个变体的转录活性。使用TRANSFAC数据库揭示了变体之间推定的TFs结合位点的差异。染色质免疫沉淀(CHIP)和荧光素酶测定分别用于评估TF结合和对转录的影响。青少年期RRP病例仅包含HPV-6vc相关变体,而在成人期RRP病例中HPV-6a变体更为普遍。 HPV-6vc参考比HPV-6a参考更具转录活性。活性FOXA1,ELF1和GATA1结合位点在分离株之间重叠可变的核苷酸位置,并影响了LCR活性。此外,我们的结果支持ELF1在转录下调中的关键作用。我们鉴定了与HPV-6早期基因表达调控有关的TF。这些因素中有许多是在癌症中突变的或是假定的癌症生物标志物,必须进一步研究。

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