首页> 美国卫生研究院文献>The Journal of Biophysical and Biochemical Cytology >Physicochemical properties of kinetoplast DNA from Crithidia acanthocephali. Crithidia luciliae and Trypanosoma lewisi
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Physicochemical properties of kinetoplast DNA from Crithidia acanthocephali. Crithidia luciliae and Trypanosoma lewisi

机译:刺桐的动植物体DNA的理化特性。十字绣菌和路氏锥虫

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摘要

The protozoa Crithidia and Trypanosoma contain within a mitochondrion a mass of DNA known as kinetoplast DNA (kDNA) which consists mainly of an association of thousands of small circular molecules of similar size held together by topological interlocking. Using kDNA from Crithidia acanthocephali, Crithidia luciliae, and Trypanosoma lewisi, physicochemical studies have been carried out with intact associations and with fractions of covalently closed single circular molecules, and of open single circular and unit length linear molecules obtained from kDNA associations by sonication, sucrose sedimentation, and cesium chloride-ethidium bromide equilibrium centrifugation. Buoyant density analyses failed to provide evidence for base composition heterogeneity among kDNA molecules within a species. The complementary nucleotide strands of kDNA molecules of all three species had distinct buoyant densities in both alkaline and neutral cesium chloride. For C. acanthocephali kDNA, these buoyant density differences were shown to be a reflection of differences in base composition between the complementary nucleotide strands. The molar ratios of adenine: thymine:guanine:cytosine, obtained from deoxyribonucleotide analyses were 16.8:41.0:28.1:14.1 for the heavy strand and 41.6:16.6:12.8:29.0 for the light strand. Covalently closed single circular molecules of C. acanthocephali (as well as intact kDNA associations of C. acanthocephali and T. lewisi) formed a single band in alkaline cesium chloride gradients, indicating their component nucleotide strands to be alkaline insensitive. Data from buoyant density, base composition, and thermal melting analyses suggested that minor bases are either rare or absent in Crithidia kDNA. The kinetics of renaturation of 32P labeled C. acanthocephali kDNA measured using hydroxyapatite chromatography were consistent with at least 70% of the circular molecules of this DNA having the same nucleotide sequence. Evidence for sequence homologies among the kDNAs of all three species was obtained from buoyant density analyses of DNA in annealed mixtures containing one component kDNA strand from each of two species.
机译:原生动物鞭毛虫和锥虫包含在线粒体内的大量DNA,称为动质体DNA(kDNA),主要由数千个大小相似的小环状分子组成,它们通过拓扑互锁保持在一起。使用棘生Cri鱼,Crisidia luciliae和Trypanosoma lewisi的kDNA,通过完整的缔合以及共价闭合的单个环状分子的一部分,以及通过超声处理,蔗糖从kDNA关联中获得的开放的单个环状和单位长度线性分子的理化研究进行了沉淀,并与氯化铯-溴化乙锭平衡离心。浮力密度分析未能提供物种中kDNA分子之间碱基组成异质性的证据。所有三种物种的kDNA分子的互补核苷酸链在碱性和中性氯化铯中均具有不同的浮力密度。对于棘头念珠菌kDNA,这些浮力密度差异显示为互补核苷酸链之间碱基组成差异的反映。从脱氧核糖核苷酸分析获得的腺嘌呤:胸腺嘧啶:鸟嘌呤:胞嘧啶的摩尔比,重链为16.8:41.0:28.1:14.1,轻链为41.6:16.6:12.8:29.0。共价封闭的棘圆线虫的单个环状分子(以及棘圆线虫和T. lewisi的完整的kDNA缔合)在碱性氯化铯梯度中形成了一条带,表明它们的组成核苷酸链对碱不敏感。浮力密度,碱基组成和热融分析的数据表明,Crithidia kDNA中的次要碱基很少或不存在。使用羟磷灰石色谱法测得的32P标记的棘头棘皮念珠菌kDNA复性的动力学与该DNA至少70%具有相同核苷酸序列的环状分子一致。所有三种物种的kDNA之间序列同源性的证据均来自对两种物种各含一种组分kDNA链的退火混合物中DNA的浮力密度分析。

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