Shaban Kholoud, Dolson Andrew, Fisher Ashley, Lessard Emma, Sauty Safia Mahabub, Yankulov Krassimir
Department of Molecular and Cellular Biology, University of Guelph, Guelph, ON, N1G2W1, Canada.
Curr Genet. 2023 Dec;69(4-6):235-249. doi: 10.1007/s00294-023-01273-3. Epub 2023 Jun 22.
Eukaryotic DNA replication is accompanied by the disassembly and reassembly of nucleosomes and the transmission of epigenetic marks to the newly assembled chromatids. Several histone chaperones, including CAF-1 and Asf1p, are central to these processes. On the other hand, replication forks pause at numerous positions throughout the genome, but it is not known if and how this pausing affects the reassembly and maintenance of chromatin structures. Here, we applied drug-free gene silencing assays to analyze the genetic interactions between CAC1, ASF1, and two genes that regulate the stability of the paused replisome (TOF1) and the resumption of elongation (RRM3). Our results show that TOF1 and RRM3 differentially interact with CAF-1 and ASF1 and that the deletions of TOF1 and RRM3 lead to reduced silencing and increased frequency of epigenetic conversions at three loci in the genome of S. cerevisiae. Our study adds details to the known activities of CAF-1 and Asf1p and suggests that the pausing of the replication fork can lead to epigenetic instability.
真核生物DNA复制伴随着核小体的解体和重新组装以及表观遗传标记向新组装染色单体的传递。包括CAF-1和Asf1p在内的几种组蛋白伴侣在这些过程中起着核心作用。另一方面,复制叉在基因组中的众多位置暂停,但尚不清楚这种暂停是否以及如何影响染色质结构的重新组装和维持。在这里,我们应用无药物基因沉默分析来分析CAC1、ASF1与两个调节暂停复制体稳定性(TOF1)和延伸恢复(RRM3)的基因之间的遗传相互作用。我们的结果表明,TOF1和RRM3与CAF-1和ASF1的相互作用存在差异,并且TOF1和RRM3的缺失导致酿酒酵母基因组中三个位点的沉默减少和表观遗传转换频率增加。我们的研究为CAF-1和Asf1p的已知活性增添了细节,并表明复制叉的暂停会导致表观遗传不稳定性。