Lewis Zachary A, Honda Shinji, Khlafallah Tamir K, Jeffress Jennifer K, Freitag Michael, Mohn Fabio, Schübeler Dirk, Selker Eric U
Institute of Molecular Biology, University of Oregon, Eugene, Oregon, 97403-1229, USA.
Genome Res. 2009 Mar;19(3):427-37. doi: 10.1101/gr.086231.108. Epub 2008 Dec 17.
Both RNAi-dependent and -independent mechanisms have been implicated in the establishment of heterochromatin domains, which may be stabilized by feedback loops involving chromatin proteins and modifications of histones and DNA. Neurospora crassa sports features of heterochromatin found in higher eukaryotes, namely cytosine methylation (5mC), methylation of histone H3 lysine 9 (H3K9me), and heterochromatin protein 1 (HP1), and is a model to investigate heterochromatin establishment and maintenance. We mapped the distribution of HP1, 5mC, H3K9me3, and H3K4me2 at 100 bp resolution and explored their interplay. HP1, H3K9me3, and 5mC were extensively co-localized and defined 44 heterochromatic domains on linkage group VII, all relics of repeat-induced point mutation. Interestingly, the centromere was found in an approximately 350 kb heterochromatic domain with no detectable H3K4me2. 5mC was not found in genes, in contrast to the situation in plants and animals. H3K9me3 is required for HP1 localization and DNA methylation in N. crassa. In contrast, we found that localization of H3K9me3 was independent of 5mC or HP1 at virtually all heterochromatin regions. In addition, we observed complete restoration of DNA methylation patterns after depletion and reintroduction of the H3K9 methylation machinery. These data show that A:T-rich RIP'd DNA efficiently directs methylation of H3K9, which in turn, directs methylation of associated cytosines.
RNA干扰依赖和非依赖机制均与异染色质结构域的建立有关,异染色质结构域可能通过涉及染色质蛋白以及组蛋白和DNA修饰的反馈环得以稳定。粗糙脉孢菌具有在高等真核生物中发现的异染色质特征,即胞嘧啶甲基化(5mC)、组蛋白H3赖氨酸9甲基化(H3K9me)和异染色质蛋白1(HP1),是研究异染色质建立和维持的模型。我们以100 bp的分辨率绘制了HP1、5mC、H3K9me3和H3K4me2的分布图,并探究了它们之间的相互作用。HP1、H3K9me3和5mC广泛共定位,并在第七连锁群上定义了44个异染色质结构域,这些都是重复诱导点突变的遗迹。有趣的是,着丝粒位于一个约350 kb的异染色质结构域中,未检测到H3K4me2。与动植物的情况不同,在基因中未发现5mC。在粗糙脉孢菌中,H3K9me3是HP1定位和DNA甲基化所必需的。相比之下,我们发现在几乎所有异染色质区域,H3K9me3的定位都独立于5mC或HP1。此外,我们观察到在耗尽并重新引入H3K9甲基化机制后,DNA甲基化模式完全恢复。这些数据表明,富含A:T的经重复诱导点突变的DNA有效地指导H3K9的甲基化,进而指导相关胞嘧啶的甲基化。