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与棉花曲叶木尔坦β卫星编码的βC1相互作用的SnRK1蛋白相关结构域的预测与验证

Prediction and Validations of Domains Involved in SnRK1 Protein Interaction With Cotton Leaf Curl Multan Betasatellite Encoded βC1.

作者信息

Kamal Hira, Minhas Fayyaz-Ul-Amir Afsar, Farooq Muhammad, Tripathi Diwaker, Hamza Muhammad, Mustafa Roma, Khan Muhammad Zuhaib, Mansoor Shahid, Pappu Hanu R, Amin Imran

机构信息

National Institute for Biotechnology and Genetic Engineering, Faisalabad, Pakistan.

Pakistan Institute of Engineering and Applied Sciences, Islamabad, Pakistan.

出版信息

Front Plant Sci. 2019 May 28;10:656. doi: 10.3389/fpls.2019.00656. eCollection 2019.

Abstract

Cotton leaf curl disease (CLCuD) caused by viruses of genus is a major constraint to cotton () production in many cotton-growing regions of the world. Symptoms of the disease are caused by Cotton leaf curl Multan betasatellite (CLCuMB) that encodes a pathogenicity determinant protein, βC1. Here, we report the identification of interacting regions in βC1 protein by using computational approaches including sequence recognition, and binding site and interface prediction methods. We show the domain-level interactions based on the structural analysis of SnRK1 protein and its domains with CLCuMB-βC1. To verify and validate the predictions, three different experimental approaches, yeast two hybrid, bimolecular fluorescence complementation and pull down assay were used. Our results showed that ubiquitin-associated domain (UBA) and autoinhibitory sequence (AIS) domains of -encoded SnRK1 are involved in CLCuMB-βC1 interaction. This is the first comprehensive investigation that combined interaction prediction followed by experimental validation of interaction between CLCuMB-βC1 and a host protein. We demonstrated that data from computational biology could provide binding site information between CLCuD-associated viruses/satellites and new hosts that lack known binding site information for protein-protein interaction studies. Implications of these findings are discussed.

摘要

由该属病毒引起的棉花卷叶病(CLCuD)是世界上许多棉花种植地区棉花生产的主要限制因素。该病症状由编码致病决定蛋白βC1的棉花卷叶木尔坦β卫星(CLCuMB)引起。在此,我们通过使用包括序列识别、结合位点和界面预测方法在内的计算方法,报告了βC1蛋白中相互作用区域的鉴定。我们基于SnRK1蛋白及其结构域与CLCuMB-βC1的结构分析展示了结构域水平的相互作用。为了验证这些预测,我们使用了三种不同的实验方法,即酵母双杂交、双分子荧光互补和下拉分析。我们的结果表明,编码SnRK1的泛素相关结构域(UBA)和自抑制序列(AIS)结构域参与了CLCuMB-βC1的相互作用。这是首次将CLCuMB-βC1与宿主蛋白之间的相互作用预测与相互作用的实验验证相结合的全面研究。我们证明,计算生物学数据可以为缺乏蛋白质-蛋白质相互作用研究已知结合位点信息的CLCuD相关病毒/卫星与新宿主之间提供结合位点信息。讨论了这些发现的意义。

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