Division of Biological Sciences, University of Missouri, Columbia, MO 65211, USA.
Epigenetics Chromatin. 2009 Nov 16;2(1):15. doi: 10.1186/1756-8935-2-15.
Heterochromatin is the tightly packaged dynamic region of the eukaryotic chromosome that plays a vital role in cellular processes such as mitosis and meiotic recombination. Recent experiments in Schizosaccharomyces pombe have revealed the structure of centromeric heterochromatin is affected in RNAi pathway mutants. It has also been shown in fission yeast that the heterochromatin barrier is traversed by RNA Pol II and that the passage of RNA Pol II through heterochromatin is important for heterochromatin structure. Thus, an intricate interaction between the RNAi machinery and RNA Pol II affects heterochromatin structure. However, the role of the RNAi machinery and RNA Pol II on the metazoan heterochromatin landscape is not known. This study analyses the interaction of the small RNA machinery and RNA Pol II on Drosophila heterochromatin structure.
The results in this paper show genetic and biochemical interaction between RNA Pol II (largest and second largest subunit) and small RNA silencing machinery components (dcr-2, ago1, ago2, piwi, Lip [D], aub and hls). Immunofluorescence analysis of polytene chromosomes from trans-heterozygotes of RNA Pol II and different mutations of the small RNA pathways show decreased H3K9me2 and mislocalization of Heterochromatin protein-1. A genetic analysis performed on these mutants showed a strong suppression of white-mottled4h position effect variegation. This was further corroborated by a western blot analysis and chromatin immunoprecipitation, which showed decreased H3K9me2 in trans-heterozygote mutants compared to wild type or single heterozygotes. Co-immunoprecipitation performed using Drosophila embryo extracts showed the RNA Pol II largest subunit interacting with Dcr-2 and dAGO1. Co-localization performed on polytene chromosomes showed RNA Pol II and dAGO1 overlapping at some sites.
Our experiments show a genetic and biochemical interaction between RNA Pol II (largest and second largest subunits) and the small RNA silencing machinery in Drosophila. The interaction has functional aspects in terms of determining H3K9me2 and HP-1 deposition at the chromocentric heterochromatin. Thus, RNA Pol II has an important role in establishing heterochromatin structure in Drosophila.
异染色质是真核染色体中紧密包装的动态区域,在有丝分裂和减数分裂重组等细胞过程中起着至关重要的作用。最近在酿酒酵母中的实验表明,RNAi 途径突变体会影响着丝粒异染色质的结构。在裂殖酵母中也表明,RNA Pol II 可以穿过异染色质,并且 RNA Pol II 通过异染色质的传递对于异染色质结构很重要。因此,RNAi 机制和 RNA Pol II 之间的复杂相互作用会影响异染色质结构。然而,RNAi 机制和 RNA Pol II 对后生动物异染色质景观的作用尚不清楚。本研究分析了小 RNA 机制和 RNA Pol II 在后生动物异染色质结构上的相互作用。
本文的结果表明,RNA Pol II(最大和第二大亚基)和小 RNA 沉默机制成分(dcr-2、ago1、ago2、piwi、Lip[D]、aub 和 hls)之间存在遗传和生化相互作用。来自 RNA Pol II 不同突变的 trans-heterozygote 以及不同小 RNA 途径突变的多线染色体的免疫荧光分析显示 H3K9me2 减少和异染色质蛋白-1 的位置错误定位。对这些突变体进行的遗传分析显示,白色斑点 4h 位置效应变异的抑制作用很强。Western blot 分析和染色质免疫沉淀进一步证实,与野生型或单杂合子相比,trans-heterozygote 突变体中的 H3K9me2 减少。使用果蝇胚胎提取物进行的共免疫沉淀显示 RNA Pol II 最大亚基与 Dcr-2 和 dAGO1 相互作用。在多线染色体上进行的共定位显示 RNA Pol II 和 dAGO1 在某些位点重叠。
我们的实验表明,在果蝇中,RNA Pol II(最大和第二大亚基)和小 RNA 沉默机制之间存在遗传和生化相互作用。这种相互作用在确定染色质异染色质的 H3K9me2 和 HP-1 沉积方面具有功能方面。因此,RNA Pol II 在果蝇异染色质结构的建立中起着重要作用。