Tasheva E S, Roufa D J
Division of Biology, Kansas State University, Manhattan 66506.
Mol Cell Biol. 1994 Sep;14(9):5636-44. doi: 10.1128/mcb.14.9.5636-5644.1994.
Densely methylated DNA sequence islands, designated DMIs, have been observed in two Chinese hamster cell chromosomal replication origins by using a PCR-based chemical method of detection. One of the origins, oriS14, is located within or adjacent to the coding sequence for ribosomal protein S14 on chromosome 2q, and the other, ori-beta, is approximately 17 kbp downstream of the dhfr (dihydrofolic acid reductase) locus on chromosome 2p. The DMI in oriS14 is 127 bp long, and the DMI in ori-beta is 516 bp long. Both DMIs are bilaterally methylated (i.e., all dCs are modified to 5-methyl dC) only in cells that are replicating their DNA. When cell growth and DNA replication are arrested, methylation of CpA, CpT, and CpC dinucleotides is lost and the sequence islands display only a subset of their originally methylated CpG dinucleotides. Several possible roles for DMI-mediated regulation of mammalian chromosomal origins are considered.
利用基于聚合酶链式反应(PCR)的化学检测方法,在中国仓鼠细胞的两个染色体复制起点中观察到了高度甲基化的DNA序列岛,即DMI。其中一个起点oriS14位于2号染色体q臂上核糖体蛋白S14编码序列内或其附近,另一个起点ori-β位于2号染色体p臂上二氢叶酸还原酶(dhfr)基因座下游约17千碱基对处。oriS14中的DMI长127碱基对,ori-β中的DMI长516碱基对。仅在进行DNA复制的细胞中,两个DMI都是双向甲基化的(即所有胞嘧啶都被修饰为5-甲基胞嘧啶)。当细胞生长和DNA复制停止时,CpA、CpT和CpC二核苷酸的甲基化消失,序列岛仅显示其最初甲基化的CpG二核苷酸的一个子集。文中考虑了DMI介导的哺乳动物染色体起点调控的几种可能作用。