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理解错义突变对人类癌症相关基因结构和功能的影响:对 COSMIC 癌症基因目录的初步计算分析。

Understanding the impacts of missense mutations on structures and functions of human cancer-related genes: A preliminary computational analysis of the COSMIC Cancer Gene Census.

机构信息

Department of Biochemistry, University of Cambridge, Cambridge, United Kingdom.

Wellcome Genome Campus, Hinxton, Cambridgeshire, United Kingdom.

出版信息

PLoS One. 2019 Jul 19;14(7):e0219935. doi: 10.1371/journal.pone.0219935. eCollection 2019.

Abstract

Genomics and genome screening are proving central to the study of cancer. However, a good appreciation of the protein structures coded by cancer genes is also invaluable, especially for the understanding of functions, for assessing ligandability of potential targets, and for designing new drugs. To complement the wealth of information on the genetics of cancer in COSMIC, the most comprehensive database for cancer somatic mutations available, structural information obtained experimentally has been brought together recently in COSMIC-3D. Even where structural information is available for a gene in the Cancer Gene Census, a list of genes in COSMIC with substantial evidence supporting their impacts in cancer, this information is quite often for a single domain in a larger protein or for a single protomer in a multiprotein assembly. Here, we show that over 60% of the genes included in the Cancer Gene Census are predicted to possess multiple domains. Many are also multicomponent and membrane-associated molecular assemblies, with mutations recorded in COSMIC affecting such assemblies. However, only 469 of the gene products have a structure represented in the PDB, and of these only 87 structures have 90-100% coverage over the sequence and 69 have less than 10% coverage. As a first step to bridging gaps in our knowledge in the many cases where individual protein structures and domains are lacking, we discuss our attempts of protein structure modelling using our pipeline and investigating the effects of mutations using two of our in-house methods (SDM2 and mCSM) and identifying potential driver mutations. This allows us to begin to understand the effects of mutations not only on protein stability but also on protein-protein, protein-ligand and protein-nucleic acid interactions. In addition, we consider ways to combine the structural information with the wealth of mutation data available in COSMIC. We discuss the impacts of COSMIC missense mutations on protein structure in order to identify and assess the molecular consequences of cancer-driving mutations.

摘要

基因组学和基因组筛选正被证明是癌症研究的核心。然而,对癌症基因编码的蛋白质结构有一个很好的了解也是非常宝贵的,特别是对于理解功能、评估潜在靶标的配体能力以及设计新药。为了补充 COSMIC 中癌症遗传学的丰富信息,这是可用的最全面的癌症体细胞突变数据库,最近在 COSMIC-3D 中汇集了实验获得的结构信息。即使在癌症基因普查中某个基因有结构信息,该普查列出了 COSMIC 中大量证据支持其在癌症中具有影响的基因,这种信息也往往是较大蛋白质中的一个单一结构域或多蛋白复合物中的一个单一亚基。在这里,我们表明,超过 60%的癌症基因普查中包含的基因预计具有多个结构域。许多基因也是多成分和膜相关的分子组装体,在 COSMIC 中记录的突变影响这些组装体。然而,只有 469 个基因产物在 PDB 中有结构表示,其中只有 87 个结构具有 90-100%的序列覆盖率,69 个结构的覆盖率小于 10%。作为填补许多情况下单个蛋白质结构和结构域缺失的知识空白的第一步,我们讨论了使用我们的管道进行蛋白质结构建模的尝试,并使用我们的两种内部方法(SDM2 和 mCSM)研究突变的影响,以及识别潜在的驱动突变。这使我们能够开始理解突变不仅对蛋白质稳定性,而且对蛋白质-蛋白质、蛋白质-配体和蛋白质-核酸相互作用的影响。此外,我们还考虑了将结构信息与 COSMIC 中可用的大量突变数据相结合的方法。我们讨论了 COSMIC 错义突变对蛋白质结构的影响,以识别和评估癌症驱动突变的分子后果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fa9/6641202/5059482028db/pone.0219935.g001.jpg

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