Bair Camden R, Kotha Lakshmi Narayan Poornima, Kajon Adriana E
Infectious Disease Program, Lovelace Respiratory Research Institute, Albuquerque, NM, United States.
Infectious Disease Program, Lovelace Respiratory Research Institute, Albuquerque, NM, United States.
Virology. 2017 May;505:139-147. doi: 10.1016/j.virol.2017.02.021. Epub 2017 Mar 1.
The unique repertoire of genes that characterizes the early region 3 (E3) of the different species of human adenovirus (HAdV) likely contributes to their distinct pathogenic traits. The function of many E3 CR1 proteins remains unknown possibly due to unidentified intrinsic properties that make them difficult to express ectopically. This study shows that the species HAdV-B- and HAdV-E-specific E3 CR1 genes can be expressed from vectors carrying the HAdV tripartite leader (TPL) sequence but not from traditional mammalian expression vectors. Insertion of the TPL sequence upstream of the HAdV-B and HAdV-E E3 CR1 open reading frames was sufficient to rescue protein expression from pCI-neo constructs in transfected 293T cells. The detection of higher levels of HAdV-B and HAdV-E E3 CR1 transcripts suggests that the TPL sequence may enhance gene expression at both the transcriptional and translational levels. Our findings will facilitate the characterization of additional AdV E3 proteins.
表征不同种类人腺病毒(HAdV)早期区域3(E3)的独特基因库可能促成了它们不同的致病特性。许多E3 CR1蛋白的功能仍然未知,这可能是由于尚未确定的内在特性使其难以异位表达。本研究表明,HAdV-B和HAdV-E特异性E3 CR1基因可从携带HAdV三联前导序列(TPL)的载体表达,但不能从传统哺乳动物表达载体表达。在HAdV-B和HAdV-E E3 CR1开放阅读框上游插入TPL序列足以挽救转染的293T细胞中pCI-neo构建体的蛋白表达。检测到更高水平的HAdV-B和HAdV-E E3 CR1转录本表明,TPL序列可能在转录和翻译水平上增强基因表达。我们的发现将有助于对其他腺病毒E3蛋白进行表征。