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关于双生病毒AC2/C2蛋白的计算研究。

Computational studies on Begomoviral AC2/C2 proteins.

作者信息

Babu Kanthalu Shagadevan Dinesh, Manoharan Prabu, Pandi Gopal

机构信息

Department of Plant Biotechnology, School of Biotechnology, Madurai Kamaraj University, Madurai, India.

Center of Excellence in Bioinformatics, School of Biotechnology, Madurai Kamaraj University, Madurai, India.

出版信息

Bioinformation. 2018 Jun 30;14(6):294-303. doi: 10.6026/97320630014294. eCollection 2018.

Abstract

Geminiviridae is a large family of circular, single stranded DNA viruses, which infects and causes devastating diseases on economically important crops. They are subdivided into nine genera. Members of the genus begomovirus encode a pathogenic protein called AC2/C2 which interacts that inactivates many plant proteins and trans-activates a number of host genes via the C-terminal transactivation domain. Hence, a sequence analysis on C-terminal region of AC2/C2 was completed. Analysis of 124 bipartite and 463 mono partite begomo viral AC2/C2 proteins revealed major differences in protein length, composition and position of acidic, aromatic and hydrophobic residues. Secondary structure analysis of AC2/C2 revealed the possible formation of C-terminal α-helix, which is similar to the acidic activation domain of many transcriptional activator proteins. Previous studies demonstrated that AC2 utilizes conserved late element (CLE) for the transactivation of viral genes and genome-wide mapping of same consensus in A. thaliana yielded 122 promoters with exact CLE consensus sequence. Analysis of protein interaction network for 106 CLE containing genes, 87 AC2 trans activated genes and 10 AC2 interacting proteins revealed a possible regulation of hundreds of host proteins which helps begomoviruses to produce a successful viral infection.

摘要

双生病毒科是一个由环状单链DNA病毒组成的大家族,可感染经济上重要的作物并引发毁灭性疾病。它们被细分为九个属。菜豆金色花叶病毒属的成员编码一种名为AC2/C2的致病蛋白,该蛋白通过C端反式激活结构域与许多植物蛋白相互作用使其失活,并反式激活多个宿主基因。因此,完成了对AC2/C2 C端区域的序列分析。对124个双分体和463个单分体菜豆金色花叶病毒AC2/C2蛋白的分析揭示了蛋白质长度、组成以及酸性、芳香族和疏水残基位置的主要差异。AC2/C2的二级结构分析揭示了C端α螺旋的可能形成,这与许多转录激活蛋白的酸性激活结构域相似。先前的研究表明,AC2利用保守晚期元件(CLE)反式激活病毒基因,在拟南芥中对相同共有序列进行全基因组定位得到了122个具有精确CLE共有序列的启动子。对106个含CLE基因、87个AC2反式激活基因和10个AC2相互作用蛋白的蛋白质相互作用网络分析揭示了数百种宿主蛋白的可能调控,这有助于菜豆金色花叶病毒产生成功的病毒感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d0d/6137562/e9f28d9cb2bc/97320630014294F1.jpg

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