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遗传距离的缩短和高复制水平会增加丁型肝炎病毒的RNA重组率。

Reduced genetic distance and high replication levels increase the RNA recombination rate of hepatitis delta virus.

作者信息

Lin Chia-Chi, Yang Zhi-Wei, Iang Shan-Bei, Chao Mei

机构信息

Division of Mcrobiology, Graduate Institue of Biomedical Sciences, College of Medicine, Chang Gung University, Tao-yang 333, Taiwan.

Division of Mcrobiology, Graduate Institue of Biomedical Sciences, College of Medicine, Chang Gung University, Tao-yang 333, Taiwan; Department of Microbiology and Immunology, College of Medicine, Chang Gung University, Tao-yang 333, Taiwan.

出版信息

Virus Res. 2015 Jan 2;195:79-85. doi: 10.1016/j.virusres.2014.08.011. Epub 2014 Aug 27.

Abstract

Hepatitis delta virus (HDV) replication is carried out by host RNA polymerases. Since homologous inter-genotypic RNA recombination is known to occur in HDV, possibly via a replication-dependent process, we hypothesized that the degree of sequence homology and the replication level should be related to the recombination frequency in cells co-expressing two HDV sequences. To confirm this, we separately co-transfected cells with three different pairs of HDV genomic RNAs and analyzed the obtained recombinants by RT-PCR followed by restriction fragment length polymorphism and sequencing analyses. The sequence divergence between the clones ranged from 24% to less than 0.1%, and the difference in replication levels was as high as 100-fold. As expected, significant differences were observed in the recombination frequencies, which ranged from 0.5% to 47.5%. Furthermore, varying the relative amounts of parental RNA altered the dominant recombinant species produced, suggesting that template switching occurs frequently during the synthesis of genomic HDV RNA. Taken together, these data suggest that during the host RNA polymerase-driven RNA recombination of HDV, both inter- and intra-genotypic recombination events are important in shaping the genetic diversity of HDV.

摘要

丁型肝炎病毒(HDV)的复制由宿主RNA聚合酶完成。由于已知HDV中会发生同源基因型间RNA重组,可能是通过依赖复制的过程,我们推测在共表达两种HDV序列的细胞中,序列同源程度和复制水平应与重组频率相关。为证实这一点,我们用三对不同的HDV基因组RNA分别共转染细胞,并通过逆转录聚合酶链反应(RT-PCR),随后进行限制性片段长度多态性分析和测序分析,来分析获得的重组体。克隆之间的序列差异范围为24%至小于0.1%,复制水平差异高达100倍。正如预期的那样,观察到重组频率存在显著差异,范围为0.5%至47.5%。此外,改变亲本RNA的相对量会改变产生的主要重组体种类,这表明在基因组HDV RNA合成过程中频繁发生模板转换。综上所述,这些数据表明,在宿主RNA聚合酶驱动的HDV RNA重组过程中,基因型间和基因型内的重组事件在塑造HDV的遗传多样性方面都很重要。

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