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Distinctive sequence patterns in metazoan and yeast nucleosomes: implications for linker histone binding to AT-rich and methylated DNA

机译:后生动物和酵母核小体中独特的序列模式:接头组蛋白与富含AT和甲基化DNA结合的含义

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Linker histones (LHs) bind to the DNA entry/exit points of nucleosomes and demonstrate preference for AT-rich DNA, although the recognized sequence patterns remain unknown. These patterns are expected to be more pronounced in metazoan nucleosomes with abundant LHs, compared to yeast nucleosomes with few LHs. To test this hypothesis, we compared the nucleosome core particle (NCP) sequences from chicken, Drosophila and yeast, extending them by the flanking sequences extracted from the genomes. We found that the known approximately 10-bp periodic oscillation of AT-rich elements goes beyond the ends of yeast nucleosomes, but is distorted in metazoan sequences where the 'out-of-phase' AT-peaks appear at the NCP ends. The observed difference is likely to be associated with sequence-specific LH binding. We therefore propose a new structural model for LH binding to metazoan nucleosomes, postulating that the highly conserved nonpolar 'wing' region of the LH globular domain (tetrapeptide GVGA) recognizes AT-rich fragments through hydrophobic interactions with the thymine methyl groups. These interactions lead to DNA bending at the NCP ends and formation of a 'stem-like' structure. The same mechanism accounts for the high affinity of LH to methylated DNA-a feature critical for stabilization of the higher-order structure of chromatin and for repression of transcription.
机译:接头组蛋白(LHs)结合到核小体的DNA进入/退出点,并显示出对富含AT的DNA的偏好,尽管公认的序列模式仍然未知。与具有少量LH的酵母核小体相比,这些模式在具有大量LH的后生核小体中有望更为明显。为了检验该假设,我们比较了来自鸡,果蝇和酵母的核小体核心颗粒(NCP)序列,并通过从基因组中提取的侧翼序列扩展了它们。我们发现,富含AT的元素的已知的大约10 bp周期性振荡超出了酵母核小体的末端,但在后相的AT-peak出现在NCP末端的后生动物序列中被扭曲了。观察到的差异可能与序列特异性LH结合有关。因此,我们提出了一种新的LH与后生核小体结合的结构模型,假定LH球状结构域(四肽GVGA)的高度保守的非极性“翼”区通过与胸腺嘧啶甲基的疏水相互作用识别富含AT的片段。这些相互作用导致DNA在NCP末端弯曲并形成“茎状”结构。相同的机制解释了LH对甲基化DNA的高度亲和力-这对于稳定染色质高阶结构和抑制转录至关重要。

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