Taylor J H
Institute of Molecular Biophysics, Florida State University, Tallahassee 32306-3015.
Bioessays. 1990 Jun;12(6):289-96. doi: 10.1002/bies.950120608.
Evidence is summarized which indicates that the DNA loop anchoring proteins in chromosomes are effectively heterodimers that stack and are fastened into a bilaterally symmetrical array along the chromonemal axis. The evidence consists primarily of the observations made twenty five to thirty years ago on the pattern of sister chromatid exchanges and the way the DNA chains are sorted in the formation of diplochromosomes in cells that have undergone endoreduplication. The evidence indicates that each chain of DNA in the single duplex, which is assumed to run the length of a chromosome, is anchored to a bilaterally symmetrical axis of heterodimers that sort the two original chains among the four derived chromatids of each diplochromosome in a very precise way. These observations are considered in the context of investigations on the nature of scaffold proteins and the loop anchorage sequences, as well as the advances being made on the nature of DNA binding proteins and the roles of topoisomerase II.
染色体中的DNA环锚定蛋白实际上是异源二聚体,它们沿染色质轴堆叠并固定成双侧对称阵列。证据主要来自于25至30年前对姐妹染色单体交换模式以及在经历了核内复制的细胞中形成双染色体时DNA链的分类方式的观察。证据表明,假设贯穿染色体全长的单双链中的每条DNA链都锚定在异源二聚体的双侧对称轴上,该轴以非常精确的方式在每个双染色体的四条衍生染色单体中对两条原始链进行分类。在对支架蛋白和环锚定序列的性质进行研究的背景下,以及在DNA结合蛋白的性质和拓扑异构酶II的作用方面取得的进展的背景下,对这些观察结果进行了考虑。