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牛病毒性腹泻病毒非结构蛋白5A膜锚定区密码子使用偏好性分析

Analysis for codon usage bias in membrane anchor of nonstructural protein 5A from BVDV.

作者信息

Gao Mingyang, Yang Xuanye, Wu Yuhu, Wang Jinqian, Hu Xinyan, Ma Zhongren, Zhou Jian-Hua

机构信息

Key Laboratory of Biotechnology and Bioengineering of State Ethnic Affairs Commission, Biomedical Research Center, Northwest Minzu University, Lanzhou.

College of Life Science and Engineering, Northwest Minzu University, Lanzhou, Gansu, China.

出版信息

J Basic Microbiol. 2023 Oct;63(10):1106-1114. doi: 10.1002/jobm.202300080. Epub 2023 Jul 5.

Abstract

The nonstructural protein 5A (NS5A) of the bovine viral diarrhea virus (BVDV) is a monotopic membrane protein. This protein can anchor to the cell membrane by an in-plane amphipathic ⍺-helix, which participates in the viral replication complex. In this study, the effects of synonymous codon usage pattern of NS5A and the overall transfer RNA (tRNA) abundance in cells on the formation of the in-plane membrane anchor of NS5A were analyzed, based on NS5A coding sequences of different BVDV genotypes. BVDV NS5A coding sequences represent the most potential for BVDV genotyping. Moreover, the nucleotide usage of BVDV NS5A dominates the genotype-specific pattern of synonymous codon usage. There is an obvious relationship between synonymous codon usage bias and the spatial conformation of the in-plane membrane anchor. Furthermore, the overall tRNA abundance profiling displays that codon positions with a high level of tRNA abundance are more than ones with a low level of tRNA abundance in the in-plane membrane anchor, implying that high translation speed probably acts on the spatial conformation of in-plane membrane anchor of BVDV NS5A. These results give a new opinion on the effect of codon usage bias in the formation of the in-plane membrane anchor of BVDV NS5A.

摘要

牛病毒性腹泻病毒(BVDV)的非结构蛋白5A(NS5A)是一种单拓扑膜蛋白。该蛋白可通过一个平面内两亲性α螺旋锚定在细胞膜上,此螺旋参与病毒复制复合体。在本研究中,基于不同BVDV基因型的NS5A编码序列,分析了NS5A同义密码子使用模式和细胞中整体转运RNA(tRNA)丰度对NS5A平面内膜锚定形成的影响。BVDV NS5A编码序列在BVDV基因分型方面具有最大潜力。此外,BVDV NS5A的核苷酸使用主导了同义密码子使用的基因型特异性模式。同义密码子使用偏好与平面内膜锚定的空间构象之间存在明显关系。此外,整体tRNA丰度分析显示,在平面内膜锚定中,tRNA丰度高的密码子位置多于tRNA丰度低的位置,这意味着高翻译速度可能作用于BVDV NS5A平面内膜锚定的空间构象。这些结果为密码子使用偏好在BVDV NS5A平面内膜锚定形成中的作用提供了新观点。

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