Liu Jie, Czajkowsky Daniel M, Liang Shoudan, Shao Zhifeng
Department of Molecular Physiology and Biological Physics, University of Virginia School of Medicine, P.O. Box 800736, Charlottesville, VA 22908, USA.
Genomics. 2008 Mar;91(3):274-80. doi: 10.1016/j.ygeno.2007.11.006.
In the budding yeast, cohesin is loaded onto the chromosome during the late G1 phase, establishes sister chromatid cohesion concomitant with DNA replication, and dissociates by the telophase. Here, using oligonucleotide tiling arrays, we show that, at the anaphase, nearly all of the cohesin binding sites contain nucleosome-free regions. The majority of these sites remain nucleosome-free throughout the cell cycle, consistent with the suggestion of a DNA-binding anchoring protein present at these sites, although such a region could also serve as part of a marker for the binding of cohesin in the next cell cycle. However, a third of these sites are remodeled in the G1 phase, being reoccupied by nucleosomes by the G1/S boundary, though their subsequent removal in the S phase appears to be independent of DNA replication. Whether this difference is a result of other functions of cohesin or of the chromatin remains to be elucidated.
在出芽酵母中,黏连蛋白在G1期晚期加载到染色体上,在DNA复制时建立姐妹染色单体黏连,并在末期解离。在此,我们使用寡核苷酸平铺阵列表明,在后期,几乎所有黏连蛋白结合位点都包含无核小体区域。这些位点中的大多数在整个细胞周期中都保持无核小体状态,这与这些位点存在DNA结合锚定蛋白的观点一致,尽管这样的区域也可能作为下一个细胞周期中黏连蛋白结合的标记的一部分。然而,这些位点中有三分之一在G1期被重塑,在G1/S边界被核小体重新占据,尽管它们在S期的后续去除似乎与DNA复制无关。这种差异是黏连蛋白的其他功能还是染色质的结果仍有待阐明。