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Role of histone modifications and early termination in pervasive transcription and antisense-mediated gene silencing in yeast

机译:组蛋白修饰和提前终止在酵母普遍转录和反义介导的基因沉默中的作用

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摘要

Most genomes, including yeast Saccharomyces cerevisiae, are pervasively transcribed producing numerous non-coding RNAs, many of which are unstable and eliminated by nuclear or cytoplasmic surveillance pathways. We previously showed that accumulation of PHO84 antisense RNA (asRNA), in cells lacking the nuclear exosome component Rrp6, is paralleled by repression of sense transcription in a process dependent on the Hda1 histone deacetylase (HDAC) and the H3K4 histone methyl transferase Set1. Here we investigate this process genome-wide and measure the whole transcriptome of various histone modification mutants in a Δrrp6 strain using tiling arrays. We confirm widespread occurrence of potentially antisense-dependent gene regulation and identify three functionally distinct classes of genes that accumulate asRNAs in the absence of Rrp6. These classes differ in whether the genes are silenced by the asRNA and whether the silencing is HDACs and histone methyl transferase-dependent. Among the distinguishing features of asRNAs with regulatory potential, we identify weak early termination by Nrd1/Nab3/Sen1, extension of the asRNA into the open reading frame promoter and dependence of the silencing capacity on Set1 and the HDACs Hda1 and Rpd3 particularly at promoters undergoing extensive chromatin remodelling. Finally, depending on the efficiency of Nrd1/Nab3/Sen1 early termination, asRNA levels are modulated and their capability of silencing is changed.
机译:包括酵母菌在内的大多数基因组都被普遍转录,产生大量非编码RNA,其中许多是不稳定的,并通过核或细胞质监视途径消除。我们先前显示,在缺乏核外泌体成分Rrp6的细胞中,PHO84反义RNA(asRNA)的积累与有义转录的抑制作用平行,该过程取决于Hda1组蛋白脱乙酰基酶(HDAC)和H3K4组蛋白甲基转移酶Set1。在这里,我们调查整个基因组的过程,并使用平铺阵列测量Δrrp6菌株中各种组蛋白修饰突变体的整个转录组。我们确认了潜在的反义依赖性基因调控的广泛发生,并确定了在没有Rrp6的情况下积累asRNA的三类功能不同的基因。这些类别在基因是否被asRNA沉默以及沉默是否与HDAC和组蛋白甲基转移酶有关方面有所不同。在具有调节潜力的asRNA的显着特征中,我们确定了Nrd1 / Nab3 / Sen1的弱早期终止,asRNA进入开放阅读框启动子的延伸以及沉默能力对Set1和HDAC Hda1和Rpd3的依赖性,特别是在经历启动子的情况下广泛的染色质重塑。最后,取决于Nrd1 / Nab3 / Sen1提前终止的效率,调节了RNA水平并改变了其沉默能力。

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