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新城疫病毒感染中的 RNA 编辑模式。

Patterns of RNA Editing in Newcastle Disease Virus Infections.

机构信息

Viral Oncogenesis group, The Pirbright Institute, Pirbright, Woking, Surrey GU24 0NF, UK.

Big Data Institute, Li Ka Shing Centre for Health Information and Discovery, Nuffield Department of Medicine, University of Oxford, Oxford OX3 7LF, UK.

出版信息

Viruses. 2020 Nov 2;12(11):1249. doi: 10.3390/v12111249.

Abstract

The expression of accessory non-structural proteins V and W in Newcastle disease virus (NDV) infections depends on RNA editing. These proteins are derived from frameshifts of the sequence coding for the P protein via co-transcriptional insertion of one or two guanines in the mRNA. However, a larger number of guanines can be inserted with lower frequencies. We analysed data from deep RNA sequencing of samples from in vitro and in vivo NDV infections to uncover the patterns of mRNA editing in NDV. The distribution of insertions is well described by a simple Markov model of polymerase stuttering, providing strong quantitative confirmation of the molecular process hypothesised by Kolakofsky and collaborators three decades ago. Our results suggest that the probability that the NDV polymerase would stutter is about 0.45 initially, and 0.3 for further subsequent insertions. The latter probability is approximately independent of the number of previous insertions, the host cell, and viral strain. However, in LaSota infections, we also observe deviations from the predicted V/W ratio of about 3:1 according to this model, which could be attributed to deviations from this stuttering model or to further mechanisms downregulating the abundance of W protein.

摘要

辅助非结构蛋白 V 和 W 在新城疫病毒(NDV)感染中的表达依赖于 RNA 编辑。这些蛋白来源于 P 蛋白编码序列通过 mRNA 中转录插入一个或两个鸟嘌呤而产生的移码。然而,更多的鸟嘌呤可以以较低的频率插入。我们分析了体外和体内 NDV 感染样本的深度 RNA 测序数据,以揭示 NDV 中 mRNA 编辑的模式。插入的分布很好地用聚合酶停顿的简单马尔可夫模型来描述,为 30 年前 Kolakofsky 及其合作者假设的分子过程提供了强有力的定量确认。我们的结果表明,NDV 聚合酶最初停顿的概率约为 0.45,进一步插入的概率约为 0.3。后一个概率大致与之前插入的数量、宿主细胞和病毒株无关。然而,在 LaSota 感染中,我们还观察到与该模型预测的 V/W 比值约为 3:1 的偏差,这可能归因于对该停顿模型的偏离或进一步下调 W 蛋白丰度的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfc7/7693698/3e4aad82725c/viruses-12-01249-g001.jpg

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