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D154Q 突变不改变 KRAS 二聚化。

D154Q Mutation does not Alter KRAS Dimerization.

机构信息

Donnelly Centre, University of Toronto, Toronto, ON, Canada; Department of Biochemistry, University of Toronto, Toronto, ON, Canada.

Department of Biochemistry, University of Toronto, Toronto, ON, Canada; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada.

出版信息

J Mol Biol. 2022 Jan 30;434(2):167392. doi: 10.1016/j.jmb.2021.167392. Epub 2021 Dec 10.

Abstract

KRAS is one of the most frequently mutated oncogenes in human cancers. Despite nearly 40 years of research, KRAS remains largely undruggable, in part due to an incomplete understanding of its biology. Recently, KRAS dimerization was discovered to play an important role in its signalling function. The KRAS D154Q mutant was described as a dimer-deficient variant that can be used to study the effect of dimerization in KRAS oncogenicity. However, we show here that KRAS D154Q homo- and heterodimerized with KRAS WT using three separate protein-protein interaction assays, and that oncogenic KRAS dimerization was not negatively impacted by the presence of a secondary D154Q mutation. In conclusion, we advise caution in using this variant to study the purpose of dimerization in KRAS oncogenic behaviour.

摘要

KRAS 是人类癌症中最常发生突变的致癌基因之一。尽管近 40 年来进行了大量研究,但 KRAS 仍然在很大程度上无法治疗,部分原因是对其生物学特性缺乏全面了解。最近,KRAS 二聚化被发现在其信号转导功能中发挥重要作用。KRAS D154Q 突变体被描述为二聚体缺陷变体,可用于研究二聚化对 KRAS 致癌性的影响。然而,我们在这里展示了 KRAS D154Q 与 KRAS WT 同源和异源二聚化,使用了三种不同的蛋白质-蛋白质相互作用测定法,并且致癌性 KRAS 二聚化不受存在次要 D154Q 突变的影响。总之,我们建议在使用该变体研究 KRAS 致癌行为中二聚化的目的时要谨慎。

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