Moazed Danesh, Rudner Adam D, Huang Julie, Hoppe Georg J, Tanny Jason C
Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
Novartis Found Symp. 2004;259:48-56; discussion 56-62, 163-9.
Gene silencing involves the assembly of DNA into specialized chromatin domains that are inaccessible to trans-acting factors and are epigenetically inherited. In the budding yeast Saccharomyces cerevisiae, silent heterochromatic DNA domains occur at telomeres, the silent mating type loci, and the rDNA repeats. At telomeres and the mating type loci, silencing requires the Sir2, Sir3 and Sir4 proteins, the conserved N-termini of histones H3 and H4, and a number of chromatin assembly factors. The Sir proteins form a multimeric complex that binds preferentially to deacetylated nucleosomes through the Sir3 and Sir4 subunits. The Sir2 subunit possesses an unusual NAD-dependent deacetylase activity that is required for silencing at each of the above loci. Recent studies have shown that silent chromatin domains are assembled in a step-wise manner involving sequential cycles of deacetylation and SIR complex binding. Sir2-dependent deacetylation is specifically required for the spreading of the complex to regions beyond nucleation sites but not for its initial binding to DNA at the mating type loci and telomeres. A distinct Sir2 complex called RENT is required for silencing at rDNA. In contrast to telomeres and the mating type loci, Sir2 activity is not required for association of RENT with rDNA.
基因沉默涉及将DNA组装成特定的染色质结构域,这些结构域对反式作用因子不可接近且可表观遗传继承。在芽殖酵母酿酒酵母中,沉默的异染色质DNA结构域出现在端粒、沉默的交配型位点和核糖体DNA重复序列处。在端粒和交配型位点,沉默需要Sir2、Sir3和Sir4蛋白、组蛋白H3和H4保守的N端以及一些染色质组装因子。Sir蛋白形成一个多聚体复合物,该复合物通过Sir3和Sir4亚基优先结合去乙酰化核小体。Sir2亚基具有一种不寻常的依赖NAD的脱乙酰酶活性,这是上述每个位点沉默所必需的。最近的研究表明,沉默染色质结构域以逐步方式组装,涉及去乙酰化和SIR复合物结合的连续循环。Sir2依赖性去乙酰化对于复合物扩散到成核位点以外的区域是特异性必需的,但对于其在交配型位点和端粒处与DNA的初始结合则不是必需的。在核糖体DNA处沉默需要一种名为RENT的独特Sir2复合物。与端粒和交配型位点不同,RENT与核糖体DNA的结合不需要Sir2活性。