Saunders M, Fitzgerald-Hayes M, Bloom K
Department of Biology, University of North Carolina, Chapel Hill 27514.
Proc Natl Acad Sci U S A. 1988 Jan;85(1):175-9. doi: 10.1073/pnas.85.1.175.
We have investigated the chromatin structure of wild-type and mutationally altered centromere sequences in the yeast Saccharomyces cerevisiae by using an indirect end-labeling mapping strategy. Wild-type centromere DNA from chromosome III (CEN3) exhibits a nuclease-resistant chromatin structure 220-250 base pairs long, centered around the conserved centromere DNA element (CDE) III. A point mutation in CDE III that changes a central cytidine to a thymidine and completely disrupts centromere function has lost the chromatin conformation typically associated with the wild-type centromere. A second conserved DNA element, CDE I, is spatially separated from CDE III by 78-86 A + T-rich base pairs, which is termed CDE II. The sequence and spatial requirements for CDE II are less stringent; alterations in CDE II length and sequence can be tolerated to a limited extent. Nuclease-resistant cores are altered in dimension in two CDE II CEN3 mutations. Two CDE I deletion mutations that retain partial centromere function also show nuclease-resistant regions of reduced size and intensity. The results from a number of such altered centromeres indicate a correlation between the presence of a protected core and centromere function.
我们通过使用间接末端标记作图策略,研究了酿酒酵母中野生型和经突变改变的着丝粒序列的染色质结构。来自第三条染色体(CEN3)的野生型着丝粒DNA呈现出一种对核酸酶有抗性的染色质结构,长度为220 - 250个碱基对,以保守的着丝粒DNA元件(CDE)III为中心。CDE III中的一个点突变将中央胞嘧啶变为胸腺嘧啶,并完全破坏了着丝粒功能,该突变已失去了通常与野生型着丝粒相关的染色质构象。第二个保守的DNA元件CDE I与CDE III在空间上被78 - 86个富含A + T的碱基对隔开,这被称为CDE II。CDE II的序列和空间要求不太严格;CDE II长度和序列的改变在一定程度上可以被容忍。在两个CDE II CEN3突变中,对核酸酶有抗性的核心在尺寸上发生了改变。两个保留部分着丝粒功能的CDE I缺失突变也显示出大小和强度降低的核酸酶抗性区域。许多这种改变的着丝粒的结果表明,受保护核心的存在与着丝粒功能之间存在相关性。