Department of Biology, Indiana University, Bloomington, IN 47405, USA.
School of Informatics and Computing, Indiana University, Bloomington, IN 47405, USA.
Nucleic Acids Res. 2015 Oct 15;43(18):8746-61. doi: 10.1093/nar/gkv766. Epub 2015 Jul 30.
Eukaryotic origins of DNA replication are bound by the origin recognition complex (ORC), which scaffolds assembly of a pre-replicative complex (pre-RC) that is then activated to initiate replication. Both pre-RC assembly and activation are strongly influenced by developmental changes to the epigenome, but molecular mechanisms remain incompletely defined. We have been examining the activation of origins responsible for developmental gene amplification in Drosophila. At a specific time in oogenesis, somatic follicle cells transition from genomic replication to a locus-specific replication from six amplicon origins. Previous evidence indicated that these amplicon origins are activated by nucleosome acetylation, but how this affects origin chromatin is unknown. Here, we examine nucleosome position in follicle cells using micrococcal nuclease digestion with Ilumina sequencing. The results indicate that ORC binding sites and other essential origin sequences are nucleosome-depleted regions (NDRs). Nucleosome position at the amplicons was highly similar among developmental stages during which ORC is or is not bound, indicating that being an NDR is not sufficient to specify ORC binding. Importantly, the data suggest that nucleosomes and ORC have opposite preferences for DNA sequence and structure. We propose that nucleosome hyperacetylation promotes pre-RC assembly onto adjacent DNA sequences that are disfavored by nucleosomes but favored by ORC.
真核生物的 DNA 复制起始受起源识别复合物(ORC)的限制,该复合物支架组装了预复制复合物(pre-RC),然后被激活以启动复制。pre-RC 的组装和激活都受到表观基因组的发育变化的强烈影响,但分子机制仍不完全明确。我们一直在研究果蝇中负责发育基因扩增的起始点的激活。在卵母细胞发生的特定时期,体细胞滤泡细胞从基因组复制转变为从六个扩增起始点的特定位置复制。先前的证据表明,这些扩增起始点是通过核小体乙酰化激活的,但这如何影响起始点染色质尚不清楚。在这里,我们使用微球菌核酸酶消化和 Illumina 测序来检查滤泡细胞中的核小体位置。结果表明,ORC 结合位点和其他必需的起始序列是核小体匮乏区(NDR)。在 ORC 结合或不结合的发育阶段,扩增子处的核小体位置非常相似,这表明成为 NDR 不足以指定 ORC 结合。重要的是,数据表明核小体和 ORC 对 DNA 序列和结构有相反的偏好。我们提出,核小体的高度乙酰化促进 pre-RC 组装到相邻的 DNA 序列上,这些序列不受核小体的青睐,但受 ORC 的青睐。