Pech M, Igo-Kemenes T, Zachau H G
Nucleic Acids Res. 1979 Sep 25;7(2):417-32. doi: 10.1093/nar/7.2.417.
A highly repetitive component of rat DNA which could not yet be enriched by density gradient centrifugation was isolated with the help of the restriction nuclease Sau3AI. This nuclease converted the bulk of the DNA to small fragments and left a repetitive DNA component as large fragments which were subsequently purified by gel filtration and electrophoresis. This DNA component which was termed rat satellite DNA I is composed of tandemly repeated 370 bp blocks. According to sequence analysis the 370 bp repeats consist of alternating 92 and 93 bp units with homologous but not identical sequences. Methylation of CpG residues was correlated to the rate of cleavage by restriction nucleases. Significant homologies exist between the sequences of rat satellite DNA I and satellite DNAs of several other organisms. The divergence of the sequence of rat satellite DNA I was discussed with respect to evolutionary considerations.
利用限制性核酸内切酶Sau3AI分离出了大鼠DNA中一种高度重复的成分,该成分尚未通过密度梯度离心法富集。这种核酸内切酶将大部分DNA转化为小片段,而留下一个重复DNA成分作为大片段,随后通过凝胶过滤和电泳对其进行纯化。这种被称为大鼠卫星DNA I的DNA成分由串联重复的370 bp片段组成。根据序列分析,370 bp重复序列由交替出现的92 bp和93 bp单元组成,它们具有同源但不相同的序列。CpG残基的甲基化与限制性核酸内切酶的切割速率相关。大鼠卫星DNA I的序列与其他几种生物的卫星DNA序列之间存在显著的同源性。从进化的角度讨论了大鼠卫星DNA I序列的差异。