首页> 美国卫生研究院文献>Biomolecules >In Silico Analysis of a Highly Mutated Gene in Cancer Provides Insight into Abnormal mRNA Splicing: Splicing Factor 3B Subunit 1K700E Mutant
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In Silico Analysis of a Highly Mutated Gene in Cancer Provides Insight into Abnormal mRNA Splicing: Splicing Factor 3B Subunit 1K700E Mutant

机译:癌症中高度突变的基因的计算机分析提供了对异常mRNA剪接的了解:剪接因子3B亚基1K700E突变体

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摘要

Cancer is the second leading cause of death worldwide. The etiology of the disease has remained elusive, but mutations causing aberrant RNA splicing have been considered one of the significant factors in various cancer types. The association of aberrant RNA splicing with drug/therapy resistance further increases the importance of these mutations. In this work, the impact of the splicing factor 3B subunit 1 (SF3B1) K700E mutation, a highly prevalent mutation in various cancer types, is investigated through molecular dynamics simulations. Based on our results, K700E mutation increases flexibility of the mutant SF3B1. Consequently, this mutation leads to i) disruption of interaction of pre-mRNA with SF3B1 and p14, thus preventing proper alignment of mRNA and causing usage of abnormal 3’ splice site, and ii) disruption of communication in critical regions participating in interactions with other proteins in pre-mRNA splicing machinery. We anticipate that this study enhances our understanding of the mechanism of functional abnormalities associated with splicing machinery, thereby, increasing possibility for designing effective therapies to combat cancer at an earlier stage.
机译:癌症是全球第二大死亡原因。该病的病因学仍然难以捉摸,但是引起异常RNA剪接的突变被认为是各种癌症类型中的重要因素之一。异常的RNA剪接与药物/治疗抗性的关联进一步增加了这些突变的重要性。在这项工作中,通过分子动力学模拟研究了剪接因子3B亚基1(SF3B1)K700E突变(在各种癌症类型中非常普遍的突变)的影响。根据我们的结果,K700E突变增加了突变体SF3B1的灵活性。因此,这种突变导致i)破坏pre-mRNA与SF3B1和p14的相互作用,从而阻止mRNA的正确排列并导致使用异常的3'剪接位点,以及ii)破坏参与与其他相互作用的关键区域的通信-mRNA剪接机制中的蛋白质。我们预计,这项研究将增强我们对与剪接机制相关的功能异常机制的理解,从而增加在较早阶段设计有效的抗癌治疗方法的可能性。

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