Howe Laboratory, Massachusetts Eye and Ear Infirmary, Department of Ophthalmology, Harvard Medical School, 243 Charles Street, Boston, Massachusetts, USA.
Department of Microbiology and Immunology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, USA.
Sci Rep. 2017 Apr 4;7(1):618. doi: 10.1038/s41598-017-00747-y.
Human adenoviruses (HAdVs) shut down host cellular cap-dependent mRNA translation while initiating the translation of viral late mRNAs in a cap-independent manner. HAdV 5' untranslated regions (5'UTRs) are crucial for cap-independent initiation, and influence mRNA localization and stability. However, HAdV translational regulation remains relatively uncharacterized. The HAdV tripartite leader (TPL), composed of three introns (TPL 1-3), is critical to the translation of HAdV late mRNA. Herein, we annotated and analyzed 72 HAdV genotypes for the HAdV TPL and another previously described leader, the i-leader. Using HAdV species D, type 37 (HAdV-D37), we show by reverse transcription PCR and Sanger sequencing that mRNAs of the HAdV-D37 E3 transcription unit are spliced to the TPL. We also identified a polycistronic mRNA for RID-α and RID-β. Analysis of the i-leader revealed a potential open reading frame within the leader sequence and the termination of this potential protein in TPL3. A potential new leader embedded within the E3 region was also detected and tentatively named the j-leader. These results suggest an underappreciated complexity of post-transcriptional regulation, and the importance of HAdV 5'UTRs for precisely coordinated viral protein expression along the path from genotype to phenotype.
人腺病毒(HAdV)在以 cap 非依赖的方式启动病毒晚期 mRNA 翻译的同时,抑制宿主细胞的 cap 依赖的 mRNA 翻译。HAdV 的 5'非翻译区(5'UTR)对 cap 非依赖的起始至关重要,并影响 mRNA 的定位和稳定性。然而,HAdV 的翻译调控仍然相对不明确。HAdV 的三分体 leader(TPL)由三个内含子(TPL1-3)组成,对于 HAdV 晚期 mRNA 的翻译至关重要。在此,我们对 72 种 HAdV 基因型的 HAdV TPL 和另一个之前描述的 leader(i-leader)进行了注释和分析。使用 HAdV 种 D、型 37(HAdV-D37),我们通过反转录 PCR 和 Sanger 测序表明,HAdV-D37 E3 转录单元的 mRNA 被拼接至 TPL。我们还鉴定了 RID-α 和 RID-β 的多顺反子 mRNA。对 i-leader 的分析揭示了 leader 序列内的一个潜在开放阅读框,以及在 TPL3 中该潜在蛋白的终止。还检测到了一个潜在的新 leader,嵌入在 E3 区域内,并暂定命名为 j-leader。这些结果表明转录后调控的复杂性被低估了,HAdV 5'UTR 对于从基因型到表型的精确协调的病毒蛋白表达非常重要。