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使用克隆的核糖体RNA基因探针区分埃及血吸虫与相关物种。

Differentiation of Schistosoma haematobium from related species using cloned ribosomal RNA gene probes.

作者信息

Walker T K, Rollinson D, Simpson A J

出版信息

Mol Biochem Parasitol. 1986 Aug;20(2):123-31. doi: 10.1016/0166-6851(86)90024-1.

Abstract

The ribosomal RNA (rRNA) gene units of Schistosoma mansoni (lateral spined eggs) and six species of schistosomes with terminal spined eggs (S. haematobium, S. curassoni, S. bovis, S. intercalatum, S. margrebowiei and S. mattheei) have been studied. The schistosome rRNA gene unit consists of a regular interspersion of the two genes encoding the large and small rRNA units with two spacers. The large spacer is not transcribed while the small spacer is part of the transcription unit. Variation in the rRNA gene unit of the species studied is demonstrated and takes three forms: First, variation in DNA sequence leads to both reduced homology in the spacer regions between species and loss or gain of restriction sites. Second, variation in the length of the transcribed spacer is demonstrated and DNA insertions of 0.2 kilobases (kb) and 0.1 kb are observed in S. mattheei and S. margrebowiei, respectively. Third, the length of the non-transcribed spacer region varies between species. S. haematobium has a 0.5 kb deletion in this region, while that of S. margrebowiei contains varying numbers of a 0.4 kb DNA insert. These interspecific variations have been shown to be conserved within species. Analysis of the rRNA genes by DNA hybridisation techniques therefore serves as a means of species identification, whereby it is possible to differentiate S. haematobium from other schistosome species with terminal spined eggs. Similarly, S. margrebowiei and S. mattheei may be clearly distinguished, although no major variation has been detected between S. curassoni, S. bovis and S. intercalatum. All these species differ from S. mansoni by the absence of certain restriction sites in the non-transcribed spacer.

摘要

对曼氏血吸虫(侧棘卵)以及六种端棘卵血吸虫(埃及血吸虫、柯氏血吸虫、牛血吸虫、间插血吸虫、Margrebowiei血吸虫和马氏血吸虫)的核糖体RNA(rRNA)基因单位进行了研究。血吸虫rRNA基因单位由编码大、小rRNA单位的两个基因与两个间隔区规则间隔排列组成。大间隔区不转录,而小间隔区是转录单位的一部分。研究的血吸虫物种rRNA基因单位存在变异,有三种形式:第一,DNA序列变异导致物种间间隔区的同源性降低以及限制性酶切位点的丢失或获得。第二,已证实转录间隔区长度存在变异,在马氏血吸虫和Margrebowiei血吸虫中分别观察到0.2千碱基(kb)和0.1 kb的DNA插入。第三,非转录间隔区的长度在物种间有所不同。埃及血吸虫在该区域有0.5 kb的缺失,而Margrebowiei血吸虫的该区域含有不同数量的0.4 kb DNA插入。这些种间变异已被证明在物种内是保守的。因此,通过DNA杂交技术分析rRNA基因可作为一种物种鉴定方法,借此能够将埃及血吸虫与其他端棘卵血吸虫物种区分开来。同样,尽管在柯氏血吸虫、牛血吸虫和间插血吸虫之间未检测到主要变异,但Margrebowiei血吸虫和马氏血吸虫可以明显区分。所有这些物种与曼氏血吸虫的不同之处在于非转录间隔区某些限制性酶切位点的缺失。

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