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海产派琴虫培养分离株中ITS和ATAN基因座的多个多态性位点。

Multiple polymorphic sites at the ITS and ATAN loci in cultured isolates of Perkinsus marinus.

作者信息

Brown Gwynne D, Hudson Karen L, Reece Kimberly S

机构信息

Virginia Institute of Marine Science, College of William and Mary, P.O. Box 1346, Gloucester Point, Virginia 23062, USA.

出版信息

J Eukaryot Microbiol. 2004 May-Jun;51(3):312-20. doi: 10.1111/j.1550-7408.2004.tb00572.x.

Abstract

Sequence analysis of genomic DNA from the protozoan parasite Perkinsus marinus at two loci revealed genetic polymorphisms within and among different cultured isolates. Genomic DNA from 12 Perkinsus marinus isolates was amplified at the internal transcribed spacer region and at an anonymous locus previously identified to contain polymorphisms by restriction fragment length polymorphism analysis. Fourteen polymorphic nucleotide positions were identified at the internal transcribed spacer region; eight in internal transcribed spacer 1 and six in internal transcribed spacer 2. Thirteen polymorphic nucleotide sites were identified within the anonymous locus. In some instances, more than three different sequences were observed at both the internal transcribed spacer region and at the anonymous locus from a single clonal isolate, suggesting the possibility of recombination in cultured cells and/or strand jumping during the polymerase chain reaction. Intra-isolate sequence variation (3.46% for the anonymous locus and 3.08% for internal transcribed spacer 1) was in several cases as high as inter-isolate sequence variation, even in one isolate where recombination was not evident. High intra- and inter-isolate variation detected at both loci demonstrates the importance of determining the genetic variation of each locus prior to development of sequence-based molecular diagnostics.

摘要

对原生动物寄生虫海派金虫(Perkinsus marinus)基因组DNA在两个位点进行的序列分析揭示了不同培养分离株内部及之间的遗传多态性。对12个海派金虫分离株的基因组DNA在内转录间隔区以及一个先前通过限制性片段长度多态性分析鉴定出含有多态性的无名位点进行了扩增。在内转录间隔区鉴定出14个多态核苷酸位置;内转录间隔区1中有8个,内转录间隔区2中有6个。在无名位点内鉴定出13个多态核苷酸位点。在某些情况下,从单个克隆分离株的内转录间隔区和无名位点都观察到了三种以上不同的序列,这表明在培养细胞中可能发生了重组和/或在聚合酶链反应过程中发生了链跳跃。分离株内的序列变异(无名位点为3.46%,内转录间隔区1为3.08%)在几种情况下与分离株间的序列变异一样高,甚至在一个没有明显重组的分离株中也是如此。在这两个位点检测到的高分离株内和分离株间变异表明,在基于序列的分子诊断方法开发之前,确定每个位点的遗传变异非常重要。

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