Christopher J. Giacoletto , Liz J. Valente , Lancer Brown , Sara Patterson , Rewatee Gokhale , Susan M. Mockus , Wayne W. Grody , Hong-Wen Deng , Jerome I. Rotter , Martin R. Schiller
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引用次数: 0
摘要
ERBB2 (HER2)是一种被充分研究的癌基因,除了在一些乳腺癌中众所周知的扩增缺陷外,还具有几种驱动突变。我们使用GigaAssay检测HER2错义突变对其受体酪氨酸激酶功能的功能影响。GigaAssay是一种模块化的高通量单锅分析系统,可同时测量数千种遗传变异的分子功能,准确度非常高。对5886个突变的活性进行了分类,明显多于以往报道的突变体。这些变异包括112个新的细胞突变,以及10个已知的和9个新的体内功能获得(GOF)突变。许多gof在序列和结构上在空间上聚集,支持EGFR异源二聚化的激活机制和近膜结构域释放激酶抑制。来自基因组数据共享(Genomic Data Commons)的患者预后回顾性分析预测,新发现的HER2 GOF变异患者的生存率高于先前发现的GOF,后者可能代表了最严重的变异。
High-throughput characterization of 5886 HER2 variants identifies 112 new in cellulo gain-of-function mutations
ERBB2 (HER2) is a well-studied oncogene with several driver mutations apart from the well-known amplification defect in some breast cancers. We used the GigaAssay to test the functional effect of HER2 missense mutations on its receptor tyrosine kinase function. The GigaAssay is a modular high-throughput one-pot assay system for simultaneously measuring molecular function of thousands of genetic variants at very high accuracy. The activities of 5886 mutations were classified, significantly more mutants than previously reported. These variants include 112 new in cellulo, as well as 10 known and 9 new in vivo gain-of-function (GOF) mutations. Many of the GOFs spatially cluster in sequence and structure, supporting the activation mechanisms of heterodimerization with EGFR and release of kinase inhibition by the juxtamembrane domain. Retrospective analysis of patient outcomes from the Genomic Data Commons predicts survival with the newly identified HER2 GOF variants is better than with previously-identified GOFs, which likely represented the most severe variants.
期刊介绍:
Genomics is a forum for describing the development of genome-scale technologies and their application to all areas of biological investigation.
As a journal that has evolved with the field that carries its name, Genomics focuses on the development and application of cutting-edge methods, addressing fundamental questions with potential interest to a wide audience. Our aim is to publish the highest quality research and to provide authors with rapid, fair and accurate review and publication of manuscripts falling within our scope.