Department of Molecular Carcinogenesis, Science Park Research Division, The University of Texas M.D. Anderson Cancer Center, Smithville, TX 78957, USA.
Department of Molecular Carcinogenesis, Science Park Research Division, The University of Texas M.D. Anderson Cancer Center, Smithville, TX 78957, USA.
Trends Cell Biol. 2014 Apr;24(4):238-46. doi: 10.1016/j.tcb.2013.10.007. Epub 2013 Nov 16.
The mystery of nuclear actin has puzzled biologists for decades largely due to the lack of defined experimental systems. However, the development of actin-containing chromatin-modifying complexes as a defined genetic and biochemical system in the past decade has provided an unprecedented opportunity to dissect the mechanism of actin in the nucleus. Although the established functions of actin mostly rely on its dynamic polymerization, the novel finding of the mechanism of action of actin in the INO80 chromatin-remodeling complex suggests a conceptually distinct mode of actin that functions as a monomer. In this review we highlight the new paradigm and discuss how actin interaction with chromatin suggests a fundamental divergence between conventional cytoplasmic actin and nuclear actin. Furthermore, we provide how this framework could be applied to investigations of nuclear actin in other actin-containing chromatin-modifying complexes.
核肌动蛋白的奥秘几十年来一直困扰着生物学家,主要是因为缺乏明确的实验系统。然而,在过去十年中,肌动蛋白包含的染色质修饰复合物的发展作为一个明确的遗传和生化系统,为剖析肌动蛋白在核中的机制提供了前所未有的机会。尽管肌动蛋白的既定功能主要依赖于其动态聚合,但肌动蛋白在 INO80 染色质重塑复合物中的作用机制的新发现表明,肌动蛋白的作用方式是一种单体,这是一种概念上截然不同的方式。在这篇综述中,我们强调了新的范例,并讨论了肌动蛋白与染色质的相互作用如何暗示了传统细胞质肌动蛋白和核肌动蛋白之间的根本差异。此外,我们还提供了如何将这一框架应用于其他肌动蛋白包含的染色质修饰复合物中核肌动蛋白的研究。