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Differential Nuclear Localization Does Not Determine the Silencing Status of Saccharomyces cerevisiae Telomeres

机译:差异核定位不能确定酿酒酵母端粒的沉默状态。

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摘要

In Saccharomyces cerevisiae, genes near telomeres are transcriptionally repressed, a phenomenon termed telomere position effect (TPE). Yeast telomeres cluster near the nuclear periphery, as do foci of proteins essential for TPE: Rap1p, Sir2-4p, and yKu70p/yKu80p. However, it is not clear if localization of telomeres to the periphery actually contributes to TPE. We examined the localization patterns of two telomeres with different levels of TPE: truncated VII-L and native VI-R. For both telomeres, localization to the nuclear periphery or to the silencing foci was neither necessary nor sufficient for TPE. Moreover, there was no correlation between TPE levels and the extent of localization. Tethering the truncated VII-L telomere to the nuclear periphery resulted in a modest increase in TPE. However, tethering did not bypass the roles of yKu70p, Sir4p, or Esc1p in TPE. Using mutations in RIF genes that bypass the role of Ku in TPE, a correlation between the level of silencing and the number of Rap1p foci present in the nucleus was observed, suggesting that Sir protein levels at telomeres determine both the level of TPE and the number of foci.
机译:在酿酒酵母中,端粒附近的基因被转录抑制,这种现象称为端粒位置效应(TPE)。酵母端粒聚集在核外围附近,TPE必需的蛋白质焦点也位于Rap1p,Sir2-4p和yKu70p / yKu80p中。但是,尚不清楚端粒在外周的定位是否确实有助于TPE。我们研究了两种具有不同TPE水平的端粒的定位模式:截短的VII-L和天然的VI-R。对于两个端粒,定位到核外围或沉默灶对于TPE既不是必需的也不是足够的。而且,TPE水平与定位程度之间没有相关性。将截短的VII-L端粒束缚到核外围会导致TPE适度增加。但是,网络共享并没有绕过yKu70p,Sir4p或Esc1p在TPE中的作用。使用绕过Ku在TPE中的作用的RIF基因突变,观察到沉默水平与细胞核中Rap1p病灶数目之间的相关性,这表明端粒的Sir蛋白水平决定了TPE的水平和数目的焦点。

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