School of Environmental Science and Engineering, Kochi University of Technology (KUT), Tosayamada, Kochi 782-8502, Japan.
Plant J. 2011 Jan;65(1):51-61. doi: 10.1111/j.1365-313X.2010.04400.x. Epub 2010 Nov 10.
In our previous work, we induced RNA interference (RNAi) against the spectinomycin resistance-conferring aadA transgene by transcribing a long inverted repeat in Chlamydomonas reinhardtii. However, after long-term culture, the level of transcripts of the inverted repeat was markedly decreased. In this study, we performed random insertional mutagenesis of the RNAi strain to identify the genes that contribute to the transcriptional silencing of the silencer construct. We succeeded in isolating several mutants showing derepression of transcription of the inverted repeat. One of these tag mutant strains, 148-10H, had a deletion of the Elongin C gene (ELC), which is a component of some E3 ubiquitin ligase complexes. In the mutant, the level of monomethyl histone H3 on lysine 9 (H3K9me1) was reduced to less than half of the parental strain, and a large portion of deacetylated H3 marks were removed from the promoter region of the silencer construct, while these repressive histone modifications and levels of methyl-CpG levels were retained in the inverted repeat region. The most probable interpretation of the above-mentioned phenomenon is that ELC is essential for stepwise extension of heterochromatin formation that is nucleated in the inverted region over the promoter region.
在我们之前的工作中,我们通过在莱茵衣藻中转录一个长的反向重复序列来诱导针对壮观霉素抗性赋予基因 aadA 的 RNA 干扰(RNAi)。然而,经过长期培养,反向重复序列的转录水平显著降低。在这项研究中,我们对 RNAi 菌株进行了随机插入突变,以鉴定有助于沉默构建体转录沉默的基因。我们成功分离到几个转录去抑制的突变体。这些标签突变体菌株之一,148-10H,缺失了 elongin C 基因(ELC),该基因是某些 E3 泛素连接酶复合物的组成部分。在突变体中,赖氨酸 9 上的单甲基组蛋白 H3(H3K9me1)的水平降低到亲本菌株的一半以下,并且沉默构建体启动子区域的去乙酰化 H3 标记大部分被去除,而这些抑制性组蛋白修饰和甲基化-CpG 水平在反向重复区域得以保留。对上述现象最可能的解释是,ELC 对于异染色质形成的逐步延伸是必不可少的,该过程以启动子区域上的反向区域为起始点。