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新城疫病毒多蛋白编码 P 基因重叠阅读框的选择特征。

Selection characterization on overlapping reading frame of multiple-protein-encoding P gene in Newcastle disease virus.

机构信息

College of Life Science, Shandong Normal University, Wenhua East Road, Shandong Province, Jinan 250014, China.

出版信息

Vet Microbiol. 2010 Aug 26;144(3-4):257-63. doi: 10.1016/j.vetmic.2009.12.029. Epub 2009 Dec 28.

Abstract

The aim of this study was to characterize the molecular evolution of P and V protein genes of the Newcastle disease virus (NDV). The P gene sequences of 55 NDV isolates, representing different chronological and geographic origins, were obtained from GenBank. In this paper, the evolution of the specific regions of the NDV P gene, encoding the P and V proteins, was analyzed. The nucleotides from the shared P/V region encoded the co-amino terminus of the two proteins, while the P-V/V-P region was respectively encoded by the nucleotides within the P ORF or the V ORF in the common sequence (after the mRNA editing site). As well, the P-cut region exclusively encoded the P protein. Finally, the P-V and V-P regions were further broken down into P1 and P2 fragments with the corresponding V1 and V2 fragments. In the P gene, the P-cut portion corresponding to the C-terminal of the P protein was the most highly conserved, while the P-V region was the most variable. This was interpreted as a lower constraint for function in the common sequence than in the unique P sequence that is known to contain an important function. Interestingly, in the common P-V/V-P function, variability of V1 was compensated by a higher conservation of the corresponding P1, and conversely for the P2/V2, which suggested that the flexibility of one ORF with less function served the purpose of allowing positive selection in the other overlapping ORF that exhibited more function.

摘要

本研究旨在对新城疫病毒(NDV)的 P 和 V 蛋白基因的分子进化进行特征分析。从 GenBank 中获得了代表不同时间和地理起源的 55 株 NDV 分离株的 P 基因序列。在本文中,分析了 NDV P 基因编码 P 和 V 蛋白的特定区域的进化。来自共享 P/V 区的核苷酸编码了两种蛋白的共同氨基末端,而 P-V/V-P 区分别由 P ORF 或 V ORF 内的核苷酸编码(在 mRNA 编辑位点之后)。此外,P 切割区专门编码 P 蛋白。最后,P-V 和 V-P 区进一步细分为具有相应 V1 和 V2 区的 P1 和 P2 片段。在 P 基因中,与 P 蛋白 C 端相对应的 P 切割部分最保守,而 P-V 区最可变。这可以解释为在共同序列中功能的约束较低,而在已知包含重要功能的独特 P 序列中约束较高。有趣的是,在共同的 P-V/V-P 功能中,V1 的变异性通过相应的 P1 更高的保守性得到补偿,而对于 P2/V2 则相反,这表明一个 ORF 的灵活性(功能较少)服务于允许另一个重叠 ORF 中具有更多功能的正选择的目的。

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