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Sequence Motifs in MADS Transcription Factors Responsible for Specificity and Diversification of Protein-Protein Interaction

机译:负责蛋白质和蛋白质相互作用的特异性和多样性的MADS转录因子中的序列基序

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Protein sequences encompass tertiary structures and contain information about specific molecular interactions, which in turn determine biological functions of proteins. Knowledge about how protein sequences define interaction specificity is largely missing, in particular for paralogous protein families with high sequence similarity, such as the plant MADS domain transcription factor family. In comparison to the situation in mammalian species, this important family of transcription regulators has expanded enormously in plant species and contains over 100 members in the model plant species Arabidopsis thaliana. Here, we provide insight into the mechanisms that determine protein-protein interaction specificity for the Arabidopsis MADS domain transcription factor family, using an integrated computational and experimental approach. Plant MADS proteins have highly similar amino acid sequences, but their dimerization patterns vary substantially. Our computational analysis uncovered small sequence regions that explain observed differences in dimerization patterns with reasonable accuracy. Furthermore, we show the usefulness of the method for prediction of MADS domain transcription factor interaction networks in other plant species. Introduction of mutations in the predicted interaction motifs demonstrated that single amino acid mutations can have a large effect and lead to loss or gain of specific interactions. In addition, various performed bioinformatics analyses shed light on the way evolution has shaped MADS domain transcription factor interaction specificity. Identified protein-protein interaction motifs appeared to be strongly conserved among orthologs, indicating their evolutionary importance. We also provide evidence that mutations in these motifs can be a source for sub- or neo-functionalization. The analyses presented here take us a step forward in understanding protein-protein interactions and the interplay between protein sequences and network evolution.
机译:蛋白质序列包含三级结构,并包含有关特定分子相互作用的信息,这些信息又决定了蛋白质的生物学功能。尤其是对于具有高序列相似性的旁系蛋白质家族,例如植物MADS结构域转录因子家族,关于蛋白质序列如何定义相互作用特异性的知识已大大缺失。与哺乳动物物种的情况相比,这个重要的转录调节因子家族在植物物种中得到了极大的扩展,在模式植物拟南芥中包含100多个成员。在这里,我们使用集成的计算和实验方法,为确定拟南芥MADS结构域转录因子家族的蛋白质-蛋白质相互作用特异性的机制提供了见识。植物MADS蛋白具有高度相似的氨基酸序列,但其二聚化模式有很大不同。我们的计算分析发现了小的序列区域,这些区域以合理的精度解释了二聚化模式中观察到的差异。此外,我们展示了该方法在其他植物物种中预测MADS域转录因子相互作用网络的有效性。在预测的相互作用基序中引入突变表明,单个氨基酸突变可以产生很大的作用,并导致特定相互作用的丧失或获得。此外,进行的各种生物信息学分析揭示了进化形成MADS结构域转录因子相互作用特异性的方式。鉴定的蛋白质-蛋白质相互作用基序在直系同源物中似乎是高度保守的,表明它们的进化重要性。我们还提供证据表明这些基序中的突变可能是亚功能化或新功能化的来源。本文介绍的分析使我们在理解蛋白质间相互作用以及蛋白质序列与网络进化之间的相互作用方面迈出了一步。

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