Segment-specific promoter activity for RNA synthesis in the genome of Oz virus, genus Thogotovirus

IF 2.8 3区 医学 Q3 VIROLOGY
Lipi Akter , Ryo Matsumura , Daisuke Kobayashi , Hiromichi Matsugo , Haruhiko Isawa , Yusuke Matsumoto
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引用次数: 0

Abstract

Oz virus (OZV), a tick-borne, six-segmented negative-strand RNA virus in the genus Thogotovirus, caused a fatal human infection in Japan in 2023. To study viral RNA synthesis, we developed an OZV minigenome assay using mammalian cells. This revealed variations in promoter activities among the six genome segments. The "distal duplex," a double-stranded RNA structure beginning at the 11th nucleotide on the 5' end and the 10th on the 3' end, was found in all segments. A factor affecting promoter activity was the base pairing between the 12th nucleotide at the 5' end and the 11th at the 3' end, forming either G:C or A:U pairs. Disruption of this pairing caused a significant loss of promoter activity, emphasizing the importance of the distal duplex with at least six consecutive base pairs. Comparative analysis of genome terminal sequences suggests similar structural variations in the promoters of other species in Thogotovirus.
Oz病毒基因组中RNA合成的片段特异性启动子活性。
Oz病毒(OZV)是一种蜱传的六段负链RNA病毒,属于Thogotovirus属,于2023年在日本引起了致命的人类感染。为了研究病毒RNA合成,我们利用哺乳动物细胞开发了OZV微小基因组测定。这揭示了6个基因组片段之间启动子活性的差异。在所有片段中都发现了“远端双链”,一种始于5‘端第11个核苷酸和3’端第10个核苷酸的双链RNA结构。影响启动子活性的一个因素是5‘端第12个核苷酸与3’端第11个核苷酸之间的碱基配对,形成G:C或A:U对。这种配对的破坏导致启动子活性的显著丧失,强调了至少具有六个连续碱基对的远端双工的重要性。基因组末端序列的比较分析表明,在其他物种的Thogotovirus启动子中也存在类似的结构变异。
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来源期刊
Virology
Virology 医学-病毒学
CiteScore
6.00
自引率
0.00%
发文量
157
审稿时长
50 days
期刊介绍: Launched in 1955, Virology is a broad and inclusive journal that welcomes submissions on all aspects of virology including plant, animal, microbial and human viruses. The journal publishes basic research as well as pre-clinical and clinical studies of vaccines, anti-viral drugs and their development, anti-viral therapies, and computational studies of virus infections. Any submission that is of broad interest to the community of virologists/vaccinologists and reporting scientifically accurate and valuable research will be considered for publication, including negative findings and multidisciplinary work.Virology is open to reviews, research manuscripts, short communication, registered reports as well as follow-up manuscripts.
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