Department of Pharmacology, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, Piscataway, NJ 08854, USA.
Proc Natl Acad Sci U S A. 2013 May 7;110(19):7654-9. doi: 10.1073/pnas.1222198110. Epub 2013 Apr 22.
FACT (facilitates chromatin transcription) is a histone chaperone that promotes chromatin recovery during transcription, with additional roles in cell differentiation. Although several models of the action of FACT during transcription have been proposed, they remain to be experimentally evaluated. Here we show that human FACT (hFACT) facilitates transcription through chromatin and promotes nucleosome recovery in vitro. FACT action depends on the presence of histone H2A/H2B dimers in the nucleosome. Kinetic analysis suggests that hFACT decreases the lifetime of nonproductive RNA polymerase II (Pol II)-nucleosome complexes and facilitates the formation of productive complexes containing nucleosomal DNA partially uncoiled from the octamer. Taken together, our data suggest that hFACT interacts with DNA-binding surfaces of H2A/H2B dimers, facilitating uncoiling of DNA from the histone octamer. Thus, hFACT-H2A/H2B interactions play a key role in overcoming the nucleosomal barrier by Pol II and promoting nucleosome survival during transcription.
FACT(促进染色质转录)是一种组蛋白伴侣,它在转录过程中促进染色质的恢复,在细胞分化中还有其他作用。尽管已经提出了几种 FACT 在转录过程中作用的模型,但它们仍有待实验评估。在这里,我们表明人类 FACT(hFACT)通过染色质促进转录,并在体外促进核小体的恢复。FACT 的作用取决于核小体中组蛋白 H2A/H2B 二聚体的存在。动力学分析表明,hFACT 缩短了非生产性 RNA 聚合酶 II(Pol II)-核小体复合物的寿命,并促进了包含部分从八聚体中解旋的核小体 DNA 的生产性复合物的形成。总之,我们的数据表明,hFACT 与 H2A/H2B 二聚体的 DNA 结合表面相互作用,促进 DNA 从组蛋白八聚体中解旋。因此,hFACT-H2A/H2B 相互作用在 Pol II 克服核小体障碍和促进转录过程中核小体存活方面发挥着关键作用。