Graduate School of Chemical Sciences and Engineering, Hokkaido University, Sapporo, Japan.
Department of Chemistry, Faculty of Science, Hokkaido University, Sapporo, Japan.
PLoS Genet. 2019 Jun 17;15(6):e1008129. doi: 10.1371/journal.pgen.1008129. eCollection 2019 Jun.
H3K9 methylation (H3K9me) is a conserved marker of heterochromatin, a transcriptionally silent chromatin structure. Knowledge of the mechanisms for regulating heterochromatin distribution is limited. The fission yeast JmjC domain-containing protein Epe1 localizes to heterochromatin mainly through its interaction with Swi6, a homologue of heterochromatin protein 1 (HP1), and directs JmjC-mediated H3K9me demethylation in vivo. Here, we found that loss of epe1 (epe1Δ) induced a red-white variegated phenotype in a red-pigment accumulation background that generated uniform red colonies. Analysis of isolated red and white colonies revealed that silencing of genes involved in pigment accumulation by stochastic ectopic heterochromatin formation led to white colony formation. In addition, genome-wide analysis of red- and white-isolated clones revealed that epe1Δ resulted in a heterogeneous heterochromatin distribution among clones. We found that Epe1 had an N-terminal domain distinct from its JmjC domain, which activated transcription in both fission and budding yeasts. The N-terminal transcriptional activation (NTA) domain was involved in suppression of ectopic heterochromatin-mediated red-white variegation. We introduced a single copy of Epe1 into epe1Δ clones harboring ectopic heterochromatin, and found that Epe1 could reduce H3K9me from ectopic heterochromatin but some of the heterochromatin persisted. This persistence was due to a latent H3K9me source embedded in ectopic heterochromatin. Epe1H297A, a canonical JmjC mutant, suppressed red-white variegation, but entirely failed to remove already-established ectopic heterochromatin, suggesting that Epe1 prevented stochastic de novo deposition of ectopic H3K9me in an NTA-dependent but JmjC-independent manner, while its JmjC domain mediated removal of H3K9me from established ectopic heterochromatin. Our results suggest that Epe1 not only limits the distribution of heterochromatin but also controls the balance between suppression and retention of heterochromatin-mediated epigenetic diversification.
H3K9 甲基化 (H3K9me) 是异染色质的保守标记物,异染色质是一种转录沉默的染色质结构。调控异染色质分布的机制知之甚少。裂殖酵母 JmjC 结构域包含蛋白 Epe1 主要通过与其相互作用的 Swi6(异染色质蛋白 1 (HP1) 的同源物)定位到异染色质,并在体内指导 JmjC 介导的 H3K9me 去甲基化。在这里,我们发现 epe1 的缺失 (epe1Δ) 在红色素积累背景下诱导了红-白斑驳表型,该背景产生了均匀的红色菌落。对分离的红色和白色菌落的分析表明,随机异位异染色质形成导致基因沉默,从而导致白色菌落的形成。此外,对红色和白色分离克隆的全基因组分析表明,epe1Δ 导致克隆之间异染色质分布不均匀。我们发现 Epe1 具有与其 JmjC 结构域不同的 N 端结构域,该结构域在裂殖酵母和 budding 酵母中都具有转录激活作用。N 端转录激活 (NTA) 结构域参与抑制异位异染色质介导的红-白斑驳。我们将 Epe1 的单个拷贝引入携带异位异染色质的 epe1Δ 克隆中,发现 Epe1 可以从异位异染色质上去除 H3K9me,但一些异染色质仍然存在。这种持久性是由于异位异染色质中嵌入的潜在 H3K9me 源。Epe1H297A,一个典型的 JmjC 突变体,抑制了红-白斑驳,但完全不能去除已经建立的异位异染色质,这表明 Epe1 以 NTA 依赖但 JmjC 独立的方式阻止异位 H3K9me 的随机从头沉积,而其 JmjC 结构域介导从已建立的异位异染色质上去除 H3K9me。我们的结果表明,Epe1 不仅限制异染色质的分布,而且还控制抑制和保留异染色质介导的表观遗传多样化之间的平衡。