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Direct measurements of the nucleosome-forming preferences of periodic DNA motifs challenge established models.

机译:直接测量周期性DNA基序的核小体形成偏好挑战已建立的模型。

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Several periodic motifs have been implicated in facilitating the bending of DNA around the histone core of the nucleosome. For example, di-nucleotides AA/TT/TA and GC at ~10-bp periods, but offset by 5 bp, are found with higher-than-expected occurrences in aligned nucleosomal DNAs in vitro and in vivo. Additionally, regularly oscillating period-10 trinucleotide motifs non-T, A/T, G and their complements have been implicated in the formation of regular nucleosome arrays. The effects of these periodic motifs on nucleosome formation have not been systematically tested directly by competitive reconstitution assays. We show that, in general, none of these period-10 motifs, except TA, in certain sequence contexts, facilitates nucleosome formation. The influence of periodic TAs on nucleosome formation is appreciable; with some of the 200-bp DNAs out-competing bulk nucleosomal DNA by more than 400-fold. Only the nucleotides immediately flanking TA influence its nucleosome-forming ability. Period-10 TA, when flanked by a pair of permissive nucleotides, facilitates DNA bending through compression of the minor groove. The free energy change for nucleosome formation decreases linearly with the number of consecutive TAs, up to eight. We suggest how these data can be reconciled with previous findings.
机译:在促进DNA围绕核小体的组蛋白核心弯曲的过程中,涉及到一些周期性的基序。例如,在体外和体内,在比对的核小体DNA中发现〜10 bp周期但被5 bp抵消的双核苷酸AA / TT / TA和GC的发生率高于预期。此外,定期振荡的10期三核苷酸基序非T,A / T,G及其补体与正常核小体阵列的形成有关。这些周期性基序对核小体形成的影响尚未通过竞争性重组测定法直接进行系统测试。我们表明,一般而言,在某些序列情况下,除了TA以外,这些10期基序均不促进核小体形成。周期性TA对核小体形成的影响是可观的。某些200 bp DNA的竞争能力超过整体核小体DNA的400倍以上。仅紧邻TA侧翼的核苷酸会影响其核小体形成能力。周期10 TA在两侧带有一对允许的核苷酸时,会通过压缩小沟而促进DNA弯曲。核小体形成的自由能变化随连续TA的数量线性减少,最多八个。我们建议如何将这些数据与以前的发现相吻合。

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