Lancrey Astrid, Joubert Alexandra, Duvernois-Berthet Evelyne, Routhier Etienne, Raj Saurabh, Thierry Agnès, Sigarteu Marta, Ponger Loic, Croquette Vincent, Mozziconacci Julien, Boulé Jean-Baptiste
Structure et Instabilité des Génomes (StrInG), Muséum National d'Histoire Naturelle, INSERM, CNRS, Alliance Sorbonne Université, 75005 Paris, France. Electronic address: https://twitter.com/AstridLancrey.
Structure et Instabilité des Génomes (StrInG), Muséum National d'Histoire Naturelle, INSERM, CNRS, Alliance Sorbonne Université, 75005 Paris, France.
J Mol Biol. 2022 Apr 15;434(7):167497. doi: 10.1016/j.jmb.2022.167497. Epub 2022 Feb 18.
The artificial 601 DNA sequence is often used to constrain the position of nucleosomes on a DNA molecule in vitro. Although the ability of the 147 base pair sequence to precisely position a nucleosome in vitro is well documented, application of this property in vivo has been explored only in a few studies and yielded contradictory conclusions. Our goal in the present study was to test the ability of the 601 sequence to dictate nucleosome positioning in Saccharomyces cerevisiae in the context of a long tandem repeat array inserted in a yeast chromosome. We engineered such arrays with three different repeat size, namely 167, 197 and 237 base pairs. Although our arrays are able to position nucleosomes in vitro, analysis of nucleosome occupancy in vivo revealed that nucleosomes are not preferentially positioned as expected on the 601-core sequence along the repeats and that the measured nucleosome repeat length does not correspond to the one expected by design. Altogether our results demonstrate that the rules defining nucleosome positions on this DNA sequence in vitro are not valid in vivo, at least in this chromosomal context, questioning the relevance of using the 601 sequence in vivo to achieve precise nucleosome positioning on designer synthetic DNA sequences.
人工合成的601 DNA序列常用于在体外限制核小体在DNA分子上的位置。尽管147个碱基对的序列在体外精确定位核小体的能力已有充分记录,但该特性在体内的应用仅在少数研究中得到探索,且得出了相互矛盾的结论。我们在本研究中的目标是,在插入酵母染色体的长串联重复阵列的背景下,测试601序列在酿酒酵母中决定核小体定位的能力。我们构建了具有三种不同重复大小(即167、197和237个碱基对)的此类阵列。尽管我们的阵列能够在体外定位核小体,但体内核小体占据情况的分析表明,沿着重复序列,核小体并非如预期那样优先定位在601核心序列上,并且测得的核小体重复长度与设计预期的长度不相符。总之,我们的结果表明,在体外定义该DNA序列上核小体位置的规则在体内无效,至少在这种染色体背景下是这样,这质疑了在体内使用601序列在设计的合成DNA序列上实现精确核小体定位的相关性。