Division of Pharmaceutical Sciences, Skaggs School of Pharmacy & Pharmaceutical Sciences, University of California, San Diego, La Jolla, CA 92093.
Department of Cellular & Molecular Medicine, School of Medicine, University of California, San Diego, La Jolla, CA 92093.
Proc Natl Acad Sci U S A. 2019 Mar 26;116(13):6120-6129. doi: 10.1073/pnas.1818163116. Epub 2019 Mar 13.
CSB/ERCC6 belongs to an orphan subfamily of SWI2/SNF2-related chromatin remodelers and plays crucial roles in gene expression, DNA damage repair, and the maintenance of genome integrity. The molecular basis of chromatin remodeling by Cockayne syndrome B protein (CSB) is not well understood. Here we investigate the molecular mechanism of chromatin remodeling by Rhp26, a CSB ortholog. The molecular basis of chromatin remodeling and nucleosomal epitope recognition by Rhp26 is distinct from that of canonical chromatin remodelers, such as imitation switch protein (ISWI). We reveal that the remodeling activities are bidirectionally regulated by CSB-specific motifs: the N-terminal leucine-latch motif and the C-terminal coupling motif. Rhp26 remodeling activities depend mainly on H4 tails and to a lesser extent on H3 tails, but not on H2A and H2B tails. Rhp26 promotes the disruption of histone cores and the release of free DNA. Finally, we dissected the distinct contributions of two Rhp26 C-terminal regions to chromatin remodeling and DNA damage repair.
CSB/ERCC6 属于 SWI2/SNF2 相关染色质重塑因子的孤儿亚家族,在基因表达、DNA 损伤修复和基因组完整性维持中发挥着关键作用。Cockayne 综合征 B 蛋白(CSB)介导的染色质重塑的分子基础尚不清楚。在这里,我们研究了 Rhp26(CSB 的同源物)介导的染色质重塑的分子机制。Rhp26 介导的染色质重塑和核小体表位识别的分子基础与典型的染色质重塑因子(如模仿开关蛋白(ISWI))明显不同。我们揭示了重塑活性是由 CSB 特异性基序:N 端亮氨酸锁模基序和 C 端偶联基序双向调节的。Rhp26 的重塑活性主要依赖于 H4 尾巴,其次依赖于 H3 尾巴,但不依赖于 H2A 和 H2B 尾巴。Rhp26 促进了组蛋白核心的破坏和游离 DNA 的释放。最后,我们剖析了 Rhp26 两个 C 端区域对染色质重塑和 DNA 损伤修复的不同贡献。