Riou G F, Yot P
Biochemistry. 1977 May 31;16(11):2390-6. doi: 10.1021/bi00630a013.
Kinetoplast DNA (kDNA) of the culture form of Trypanosoma cruzi is cleaved by restriction endonucleases (HpaII, HindII, EcoRI, and HaeIII). The analysis of the cleavage patterns proves that the minicircles (free circulargenome units) are heterogeneous in base sequences. The same results are obtained with the complex kDNA network which is composed of the association of minicircles and linear molecules. Kinetic studies of the renaturation of kDNA previously cleaved by HpaII into fragments of the genome unit size show at least two populations of molecules. About 75% of these molecules correspond to the fast renaturing population having the molecular complexity of the minicircles. The molecules of the slow renaturing population have a much higher molecular complexity than the minicircles and do not seem to be related to the majority of the long linear molecules.
克氏锥虫培养形式的动基体DNA(kDNA)可被限制性内切酶(HpaII、HindII、EcoRI和HaeIII)切割。对切割模式的分析证明,微小环(游离环状基因组单位)在碱基序列上是异质的。由微小环和线性分子缔合组成的复杂kDNA网络也得到了相同的结果。对先前被HpaII切割成基因组单位大小片段的kDNA复性动力学研究表明,至少有两类分子群体。这些分子中约75%对应于具有微小环分子复杂性的快速复性群体。缓慢复性群体的分子比微小环具有更高的分子复杂性,似乎与大多数长线性分子无关。