van Herwerden L, Blair D, Agatsuma T
Zoology Department, James Cook University, Townsville, Queensland, 4811, Australia.
Mol Phylogenet Evol. 1999 Jun;12(1):67-73. doi: 10.1006/mpev.1998.0572.
We investigated the utility of the ribosomal first internal transcribed spacer (ITS1) for phylogenetic studies on trematodes of the genus Paragonimus. Numerous clones containing ITS1 PCR products were sequenced for P. miyazakii, P. macrorchis, and members of the P. ohirai and P. westermani species complexes. Some additional data were obtained by direct sequencing of PCR products. The ITS1 is composed of three distinct regions: the short 5' end, followed by a tract of approximately 120 nucleotides which occurs a variable number of times in tandem, and the 3' region, which lacks repeats and is referred to as the "post-repeat" fragment. Sequences from all three regions can be aligned among the species studied. Our initial hypothesis, that the post-repeat region would be valuable for phylogenetic studies within the P. westermani complex, was proved wrong. Intraindividual sequence variation in P. westermani was sometimes greater than between individuals of the species complex. In the P. ohirai species complex, however, sequence variation within individuals was minimal. Possible reasons for these observations are discussed. We also wished to determine whether the length variants sequenced were the dominant variants present in Paragonimus species. This was done by probing Southern blots of genomic digests with an ITS1 fragment which lacks repeat sequences. There is generally greater abundance of large variants, with much lower abundance of small variants, such as those sequenced. Differences in ITS1 lengths are attributed largely to differing numbers of repeats, though some exceptions (which are discussed) were found.
我们研究了核糖体第一内部转录间隔区(ITS1)在肺吸虫属吸虫系统发育研究中的实用性。对宫崎肺吸虫、巨睾肺吸虫以及大平肺吸虫和卫氏肺吸虫物种复合体的成员,对大量含有ITS1 PCR产物的克隆进行了测序。通过对PCR产物直接测序获得了一些额外数据。ITS1由三个不同区域组成:短的5'端,接着是一段约120个核苷酸的片段,该片段串联出现可变次数,以及3'区域,该区域没有重复序列,被称为“重复后”片段。所研究物种的所有三个区域的序列都可以进行比对。我们最初的假设,即重复后区域对卫氏肺吸虫复合体的系统发育研究有价值,被证明是错误的。卫氏肺吸虫个体内的序列变异有时大于物种复合体内个体之间的变异。然而,在大平肺吸虫物种复合体内,个体内的序列变异最小。讨论了这些观察结果的可能原因。我们还希望确定测序的长度变异体是否是肺吸虫物种中存在的主要变异体。这是通过用缺乏重复序列的ITS1片段探测基因组消化产物的Southern印迹来完成的。通常大变异体的丰度更高,而小变异体(如测序的那些)的丰度要低得多。ITS1长度的差异主要归因于重复次数的不同,不过也发现了一些例外情况(将进行讨论)。