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H5N1血凝素裂解位点的遗传学见解。

Genetic insight of the H5N1 hemagglutinin cleavage site.

作者信息

Guo XiaoLi, Zhu YiSheng, Li YiXue, Shi Ping, Zhou HaoKui, Yao JinSong, Huang ZhenDe, Wei DongQing

机构信息

College of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, 200240 China.

出版信息

Chin Sci Bull. 2007;52(17):2374-2379. doi: 10.1007/s11434-007-0374-y.

Abstract

The cleavability of the hemagglutinin (HA) plays a major role in virulence of avian influenza viruses. Detailed analyses of the cleavage sequences and their evolution would give insights into the high pathogenicity of the H5N1 virus. HA segments were visually identifiable in the cellular automata (CA) image, and a feature gene segment (FGS) was only found in H5N1 rather than any other subtype. This FGS is a 30-bp gene segment mainly consisting of 'A' and 'G'. When translated into amino acids the FGS converted into a sequence of mainly basic amino acids with positive charges. This feature amino acid segment (FAAS) was located in the cleavage site loop of HA which was potentially cleavable by various proteases. The 3D structure of H5N1 HA was reconstructed using homology modelling. It was found that the cleavage site loop was well exposed to potential proteases. The molecular surfaces were reconstructed to study how mutation and deletion of some amino acids in the FAAS affected the charge distribution. It was found that some mutations had severely changed the landscape of the charge distribution. Statistical analyses of FAAS were made with respect to when and where the H5N1 viruses were found. In 2005, there were less un-mutated FAAS than the other years according to temporal evolution, and more mutated FAAS appeared in China than other regions according to geographic distribution. These results are helpful for exploring the evolution of virus high pathogenicity.

摘要

血凝素(HA)的可切割性在禽流感病毒的毒力中起主要作用。对切割序列及其进化的详细分析将有助于深入了解H5N1病毒的高致病性。在细胞自动机(CA)图像中可直观识别HA片段,并且仅在H5N1中而非任何其他亚型中发现了一个特征基因片段(FGS)。该FGS是一个主要由“A”和“G”组成的30个碱基对的基因片段。当翻译成氨基酸时,FGS转化为主要由带正电荷的碱性氨基酸组成的序列。这个特征氨基酸片段(FAAS)位于HA的可切割位点环中,该环可能被各种蛋白酶切割。使用同源建模重建了H5N1 HA的三维结构。发现可切割位点环很好地暴露于潜在的蛋白酶。重建分子表面以研究FAAS中某些氨基酸的突变和缺失如何影响电荷分布。发现一些突变严重改变了电荷分布格局。对发现H5N1病毒的时间和地点进行了FAAS的统计分析。根据时间演变,2005年未突变的FAAS比其他年份少,根据地理分布,中国出现的突变FAAS比其他地区多。这些结果有助于探索病毒高致病性的演变。

相似文献

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Genetic insight of the H5N1 hemagglutinin cleavage site.H5N1血凝素裂解位点的遗传学见解。
Chin Sci Bull. 2007;52(17):2374-2379. doi: 10.1007/s11434-007-0374-y.

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