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动质体DNA的结构。1. 纤细短膜虫的微小环在碱基序列上是异质的。

The structure of kinetoplast DNA. 1. The mini-circles of Crithidia lucilae are heterogeneous in base sequence.

作者信息

Kleisen M C, Borst P, Weijers P J

出版信息

Eur J Biochem. 1976 Apr 15;64(1):141-51. doi: 10.1111/j.1432-1033.1976.tb10282.x.

Abstract

We have analysed limit digests of mini-circles from kinetoplast DNA of Crithidia luciliae by gel electrophoresis. Endonucleases HapII and AluI cut the circles into at least 37 and 21 fragments, respectively, and leave no circles intact. In both cases the added molecular weights of the fragments, estimated from mobility in gels, exceeds 18 X 10(6), i.e. more than 12 times the molecular weight of the mini-circle DNA. Endonucleases HindII + III, EcoRI and HpaI cut only part of the circles. These results show that the mini-circles are heterogeneous in base sequence. Different sequence classes are present in different amounts. DNA-DNA renaturation analysis of mini-circle DNA yields a complexity of about 3 X 10(6), i.e. twice the molecular weight on one mini-circle. The delta tm of native and renatured duplexes is about 1 degree C, showing that the sequence heterogeneity is a micro-heterogeneity. Electron microscopy, gel electrophoresis and sedimentation analysis show that the circles that are not cut by endonucleases HindII + III remain catenated in very large associations. These associations lack the 'rosette' structures and the long edge loops characteristic of intact kinetoplast DNA. This suggests that the mini-circle classes cut by endonucleases HindII + III are present throughout the network and that the maxi-circle component of the network (see accompanying paper) is not essential to hold the network together. Prolonged electrophoresis on 1.5% or 2% agarose gels resolves the open mini-circles into three and linearized mini-circles into four bands, present in different amounts. We conclude that the mini-circles are also heterogeneous in size, the difference in size between the two extreme size classes being 4% of the contour length. Digestion with endonuclease HapII shows that at least three out of these four bands differ in sequence. Possible mechanisms that could account for the micro-heterogeneity in sequence of mini-circles are discussed.

摘要

我们通过凝胶电泳分析了鲁氏锥虫动质体DNA微小环的限制性酶切片段。核酸内切酶HapII和AluI分别将这些环切成至少37个和21个片段,且没有完整的环留存。在这两种情况下,根据凝胶中的迁移率估算,片段的分子量之和超过18×10⁶,即超过微小环DNA分子量的12倍。核酸内切酶HindII + III、EcoRI和HpaI仅切割部分环。这些结果表明微小环的碱基序列是异质的。不同的序列类别数量不同。微小环DNA的DNA - DNA复性分析得出的复杂度约为3×10⁶,即一个微小环分子量的两倍。天然双链和复性双链的Δtm约为1℃,表明序列异质性是微异质性。电子显微镜、凝胶电泳和沉降分析表明,未被核酸内切酶HindII + III切割的环以非常大的聚集体形式连环存在。这些聚集体缺乏完整动质体DNA特有的“玫瑰花结”结构和长边缘环。这表明被核酸内切酶HindII + III切割的微小环类别遍布整个网络,并且网络的大环成分(见随附论文)对于维持网络结构并非必不可少。在1.5%或2%琼脂糖凝胶上进行长时间电泳,可将开环微小环分离成三条带,线性化微小环分离成四条带,它们的含量各不相同。我们得出结论,微小环在大小上也是异质的,两个极端大小类别的大小差异为轮廓长度的4%。用核酸内切酶HapII消化表明,这四条带中至少有三条在序列上不同。文中讨论了可能导致微小环序列微异质性的机制。

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