Department of Biology, The Johns Hopkins University, Baltimore, MD, USA.
Carnegie Institution for Science, Department of Embryology, Baltimore, MD, USA.
Nat Struct Mol Biol. 2019 Aug;26(8):732-743. doi: 10.1038/s41594-019-0269-z. Epub 2019 Jul 29.
Many stem cells undergo asymmetric division to produce a self-renewing stem cell and a differentiating daughter cell. Here we show that, similarly to H3, histone H4 is inherited asymmetrically in Drosophila melanogaster male germline stem cells undergoing asymmetric division. In contrast, both H2A and H2B are inherited symmetrically. By combining super-resolution microscopy and chromatin fiber analyses with proximity ligation assays on intact nuclei, we find that old H3 is preferentially incorporated by the leading strand, whereas newly synthesized H3 is enriched on the lagging strand. Using a sequential nucleoside analog incorporation assay, we detect a high incidence of unidirectional replication fork movement in testes-derived chromatin and DNA fibers. Biased fork movement coupled with a strand preference in histone incorporation would explain how asymmetric old and new H3 and H4 are established during replication. These results suggest a role for DNA replication in patterning epigenetic information in asymmetrically dividing cells in multicellular organisms.
许多干细胞通过不对称分裂产生自我更新的干细胞和分化的子细胞。在这里,我们表明,与 H3 类似,组蛋白 H4 在经历不对称分裂的黑腹果蝇雄性生殖干细胞中也是不对称遗传的。相比之下,H2A 和 H2B 都是对称遗传的。通过将超分辨率显微镜和染色质纤维分析与完整核的邻近连接测定相结合,我们发现旧 H3 优先被前导链掺入,而新合成的 H3 则在滞后链上富集。使用连续核苷类似物掺入测定法,我们在睾丸衍生的染色质和 DNA 纤维中检测到单向复制叉运动的高发生率。偏向性的叉运动加上组蛋白掺入中的链偏好性,将解释在复制过程中如何建立不对称的新旧 H3 和 H4。这些结果表明 DNA 复制在多细胞生物中不对称分裂细胞的表观遗传信息模式化中发挥作用。