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Artificial nucleosome positioning sequences tested in yeast minichromosomes: a strong rotational setting is not sufficient to position nucleosomes in vivo.

机译:在酵母微染色体中测试的人工核小体定位序列:强旋转设置不足以在体内定位核小体。

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摘要

DNA sequences that support bending around the histone octamer ('rotational setting') are considered to be a major determinant of nucleosome positions. TG5 is an artificial positioning sequence containing 100 bp of an (A/T)3NN(G/C)3NN motif repeated with a 10 bp period. It provides a strong rotational setting and is superior to natural sequences in nucleosome formation in vitro [Shrader, T.E. and Crothers, D.M. (1989) Proc. Natl. Acad. Sci. USA, 86, 7418-7422]. To investigate the contribution of the rotational setting to nucleosome positioning in vivo, TG sequences were inserted in a nucleosome, at the edge of a nucleosome and in a nuclease sensitive region of yeast minichromosomes and the chromatin structures were analysed. In none of the constructs were TG sequences folded in a positioned nucleosome, demonstrating that the rotational setting played a subordinate role in the rough positioning in vivo. The rotational setting might fine tune the positions. Positioned nucleosomes were found overlapping the ends of TG, indicating that a discontinuity of the 10 bp periodicity of (A/T)3 and (G/C)3 near the centre of a nucleosome might be favourable for positioning and serve as a translational signal.
机译:支持围绕组蛋白八聚体弯曲的DNA序列(“旋转设置”)被认为是核小体位置的主要决定因素。 TG5是一个人工定位序列,包含100 bp的(A / T)3NN(G / C)3NN基序,重复10 bp。它提供了强大的旋转设置,并且在体外核小体形成方面优于自然序列[Shrader,T.E。和克罗瑟斯(D.M.) (1989年)过程。 Natl。学院科学美国,86,7418-7422]。为了研究旋转设置对体内核小体定位的贡献,将TG序列插入核小体中,核小体的边缘和酵母微染色体的核酸酶敏感区中,并分析了染色质结构。 TG序列均未在定位的核小体中折叠,表明旋转设置在体内粗略定位中起从属作用。旋转设置可能会微调位置。发现定位的核小体与TG的末端重叠,这表明靠近核小体中心的(A / T)3和(G / C)3的10 bp周期的不连续性可能有利于定位并充当翻译信号。

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