Laboratory of Chromosome and Cell Biology, The Rockefeller University, New York, NY 10065;
Institut Curie, PSL Research University, CNRS, UMR 144, F-75005 Paris, France.
Proc Natl Acad Sci U S A. 2021 Mar 9;118(10). doi: 10.1073/pnas.2015634118.
Chromosome segregation relies on centromeres, yet their repetitive DNA is often prone to aberrant rearrangements under pathological conditions. Factors that maintain centromere integrity to prevent centromere-associated chromosome translocations are unknown. Here, we demonstrate the importance of the centromere-specific histone H3 variant CENP-A in safeguarding DNA replication of alpha-satellite repeats to prevent structural aneuploidy. Rapid removal of CENP-A in S phase, but not other cell-cycle stages, caused accumulation of R loops with increased centromeric transcripts, and interfered with replication fork progression. Replication without CENP-A causes recombination at alpha-satellites in an R loop-dependent manner, unfinished replication, and anaphase bridges. In turn, chromosome breakage and translocations arise specifically at centromeric regions. Our findings provide insights into how specialized centromeric chromatin maintains the integrity of transcribed noncoding repetitive DNA during S phase.
染色体分离依赖于着丝粒,但它们的重复 DNA 在病理条件下往往容易发生异常重排。目前尚不清楚哪些因素能够维持着丝粒的完整性,以防止与着丝粒相关的染色体易位。在这里,我们证明了着丝粒特异性组蛋白 H3 变体 CENP-A 在保护α-卫星重复序列的 DNA 复制方面的重要性,以防止结构非整倍体。在 S 期而非其他细胞周期阶段快速去除 CENP-A 会导致 R 环积累,增加着丝粒转录物,并干扰复制叉的进展。没有 CENP-A 的复制会导致以 R 环依赖的方式在α-卫星上发生重组、未完成的复制和后期桥。反过来,染色体断裂和易位特异性地发生在着丝粒区域。我们的研究结果提供了深入了解专门的着丝粒染色质如何在 S 期维持转录非编码重复 DNA 的完整性。