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Genome-wide identification and characterization of replication origins by deep sequencing

机译:通过深度测序对全基因组复制起点进行鉴定和表征

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摘要

Background: DNA replication initiates at distinct origins in eukaryotic genomes, but the genomic features that define these sites are not well understood. Results: We have taken a combined experimental and bioinformatic approach to identify and characterize origins of replication in three distantly related fission yeasts: Schizosaccharomyces pombe, Schizosaccharomyces octosporus and Schizosaccharomyces japonicus. Using single-molecule deep sequencing to construct amplification-free high- resolution replication profiles, we located origins and identified sequence motifs that predict origin function. We then mapped nucleosome occupancy by deep sequencing of mononucleosomal DNA from the corresponding species, finding that origins tend to occupy nucleosome-depleted regions. Conclusions: The sequences that specify origins are evolutionarily plastic, with low complexity nucleosome- excluding sequences functioning in S. pombe and S. octosporus, and binding sites for trans-acting nucleosome- excluding proteins functioning in S. japonicus. Furthermore, chromosome-scale variation in replication timing is conserved independently of origin location and via a mechanism distinct from known heterochromatic effects on origin function. These results are consistent with a model in which origins are simply the nucleosome-depleted regions of the genome with the highest affinity for the origin recognition complex. This approach provides a general strategy for understanding the mechanisms that define DNA replication origins in eukaryotes.
机译:背景:DNA复制起始于真核生物基因组中的不同起点,但定义这些位点的基因组特征尚不十分清楚。结果:我们采取了一种结合实验和生物信息学的方法,来鉴定和表征三种远缘相关裂变酵母中的复制起点:裂殖酵母,裂殖酵母和日本裂殖酵母。使用单分子深度测序构建无扩增的高分辨率复制谱,我们找到了起源并鉴定了预测起源功能的序列基序。然后,我们通过对来自相应物种的单核糖体DNA进行深度测序来绘制核小体的占据图,发现其起源往往会占据核小体耗尽的区域。结论:指定起源的序列在进化上是可塑性的,具有低复杂性的核小体(不包括在粟酒裂殖酵母和八孔链霉菌中起作用)的序列,以及反式作用的核小体(不含蛋白质)在日本血吸虫中起作用的结合位点。此外,复制时机的染色体尺度变化与起点位置无关,并且通过不同于已知异源作用于起点功能的机制得以保存。这些结果与一个模型一致,在该模型中,起源只是对起源识别复合物具有最高亲和力的基因组的核小体耗尽区域。该方法为理解真核生物中DNA复制起点的机制提供了一般策略。

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