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Spatial telomere organization and clustering in yeast Saccharomyces cerevisiae nucleus is generated by a random dynamics of aggregation–dissociation

机译:酵母酿酒酵母细胞核中的空间端粒组织和聚集是由聚集-解离的随机动力学产生的

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摘要

Spatial and temporal behavior of chromosomes and their regulatory proteins is a key control mechanism in genomic function. This is exemplified by the clustering of the 32 budding yeast telomeres that form foci in which silencing factors concentrate. To uncover the determinants of telomere distribution, we compare live-cell imaging with a stochastic model of telomere dynamics that we developed. We show that random encounters alone are inadequate to produce the clustering observed in vivo. In contrast, telomere dynamics observed in vivo in both haploid and diploid cells follows a process of dissociation–aggregation. We determine the time that two telomeres spend in the same cluster for the telomere distribution observed in cells expressing different levels of the silencing factor Sir3 protein, limiting for telomere clustering. We conclude that telomere clusters, their dynamics, and their nuclear distribution result from random motion, aggregation, and dissociation of telomeric regions, specifically determined by the amount of Sir3.
机译:染色体及其调节蛋白的时空行为是基因组功能的关键控制机制。这可以通过32个萌芽的酵母端粒的聚集来举例说明,这些端粒形成了沉默因子集中的焦点。为了揭示端粒分布的决定因素,我们将活细胞成像与我们开发的端粒动力学随机模型进行了比较。我们表明,仅随机遇到是不足以产生体内观察到的群集。相反,在体内在单倍体和二倍体细胞中观察到的端粒动力学遵循解离-聚集过程。我们确定在表达不同水平的沉默因子Sir3蛋白的细胞中观察到的端粒分布,两个端粒在同一簇中停留的时间,从而限制了端粒的簇集。我们得出的结论是,端粒簇,其动力学及其核分布是由端粒区域的随机运动,聚集和解离产生的,具体取决于Sir3的量。

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