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结膜黑色素瘤驱动基因突变的结构蛋白分析。

Structural Protein Analysis of Driver Gene Mutations in Conjunctival Melanoma.

机构信息

Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, FL 33136, USA.

Department of Molecular Medicine and USF Health Byrd Alzheimer's Research Institute, Morsani College of Medicine, University of South Florida, Bruce B. Downs Blvd., MDC07, Tampa, FL 33612, USA.

出版信息

Genes (Basel). 2021 Oct 15;12(10):1625. doi: 10.3390/genes12101625.

Abstract

In recent years, there has been tremendous enthusiasm with respect to detailing the genetic basis of many neoplasms, including conjunctival melanoma (CM). We aim to analyze five proteins associated with CM, namely BRAF, NRAS, c-KIT, NF1, and PTEN. We evaluated each protein for its intrinsically disordered protein regions (IDPRs) and its protein-protein interactions (PPI) with the Predictor of Natural Disordered Protein Regions (PONDR) and the Search Tool for the Retrieval of Interacting Genes (STRING). Our PONDR analysis found high levels of IDPRs in all five proteins with mutations linked to CM. The highest levels of IDPRs were in BRAF (45.95%), followed by PTEN (31.76%), NF1 (22.19%), c-KIT (21.82%), and NRAS (14.81%). Our STRING analysis found that each of these five proteins had more predicted interactions then expected (-value < 1.0 × 10). Our analysis demonstrates that the mutations linked to CM likely affected IDPRs and possibly altered their highly complex PPIs. Quantifying IDPRs in BRAF, NRAS, c-KIT, NF1, and PTEN and understanding these protein regions are important processes as IDPRs can be possible drug targets for novel targeted therapies for treating CM.

摘要

近年来,人们对详细研究许多肿瘤的遗传基础产生了浓厚的兴趣,包括结膜黑色素瘤(CM)。我们旨在分析与 CM 相关的五种蛋白质,即 BRAF、NRAS、c-KIT、NF1 和 PTEN。我们使用蛋白质无序区域预测器(PONDR)和检索相互作用基因的搜索工具(STRING)评估了每种蛋白质的固有无序区域(IDPR)及其蛋白质-蛋白质相互作用(PPI)。我们的 PONDR 分析发现,与 CM 相关的突变与所有五种蛋白质的高 IDPR 水平有关。IDPR 水平最高的是 BRAF(45.95%),其次是 PTEN(31.76%)、NF1(22.19%)、c-KIT(21.82%)和 NRAS(14.81%)。我们的 STRING 分析发现,这五种蛋白质中的每一种都具有比预期更多的预测相互作用(-值<1.0×10)。我们的分析表明,与 CM 相关的突变可能影响了 IDPR,并可能改变了它们高度复杂的 PPI。定量分析 BRAF、NRAS、c-KIT、NF1 和 PTEN 中的 IDPR 并了解这些蛋白质区域是非常重要的,因为 IDPR 可能是治疗 CM 的新型靶向治疗的潜在药物靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/003b/8535873/290af281a386/genes-12-01625-g001.jpg

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