Funk M, Hegemann J H, Philippsen P
Institute of Microbiology and Molecular Biology, Justus Liebig University, Giessen, Federal Republic of Germany.
Mol Gen Genet. 1989 Oct;219(1-2):153-60. doi: 10.1007/BF00261171.
Isolated nuclei of Saccharomyces cerevisiae were incubated with five restriction nucleases. Out of the twenty-one recognition sequences for these nucleases in the centromere region of chromosome XIV, only five are accessible to cleavage. These sites map 11 bp and 74 bp to the left and 27 bp, 41 bp and 290 bp to the right, respectively, of the boundaries of the 118 bp functional CEN14 DNA sequence. The distance between the sites accessible to cleavage and closest to CEN14 is 156 bp, suggesting this is the maximal size of DNA protected in CEN14 chromatin. The DNA in CEN14 chromatin protected against cleavage with DNase I and micrococcal nuclease overlaps almost completely with this region. Hypersensitive regions flanking both sides are approximately 60 bp long. Analyses of other S. cerevisiae centromeres with footprinting techniques in intact cells or nucleolytic cleavages in isolated nuclei are discussed in relation to our results. We conclude that structural data of chromatin obtained with restriction nucleases are reliable and that the structure of CEN14 chromatin is representative for S. cerevisiae centromeres.
将酿酒酵母的分离细胞核与五种限制性核酸内切酶一起孵育。在第十四条染色体着丝粒区域中这些核酸酶的21个识别序列中,只有5个可被切割。这些位点分别位于118 bp功能性CEN14 DNA序列边界的左侧11 bp和74 bp处,以及右侧27 bp、41 bp和290 bp处。可被切割且最接近CEN14的位点之间的距离为156 bp,这表明这是CEN14染色质中受保护的DNA的最大尺寸。CEN14染色质中免受DNA酶I和微球菌核酸酶切割的DNA几乎与该区域完全重叠。两侧的超敏区域约为60 bp长。结合我们的结果,讨论了在完整细胞中用足迹技术或在分离细胞核中进行核酸酶切割对其他酿酒酵母着丝粒的分析。我们得出结论:用限制性核酸内切酶获得的染色质结构数据是可靠的,并且CEN14染色质的结构代表了酿酒酵母着丝粒。