Blok V C, Malloch G, Harrower B, Phillips M S, Vrain T C
J Nematol. 1998 Jun;30(2):262-74.
The relationships among a number of populations of Globodera pallida from Britian, the Netherlands, Germany, Switzerland, and South America were examined using PCR amplification of the ribosomal cistron between the 18S and 28S genes that include the two intergenic spacer regions (ITS1 and ITS2) and the 5.8S gene. Amplifications produced a similar-sized product of 1150 bp from all populations. Digestion of the amplified fragment with a number of restriction enzymes showed differences among the populations. The restriction enzyme RsaI distinguished the most populations. The RFLP patterns revealed by this enzyme were complex and could have arisen from heterogeneity between individuals within populations and from differences between the repeats of an individual. Sequence analysis from six of the populations, together with RFLP analysis of PCR products, shows that there is intraspecific variation in the rDNA of G. pallida.
利用对核糖体顺反子中18S和28S基因之间包括两个基因间隔区(ITS1和ITS2)以及5.8S基因进行PCR扩增的方法,研究了来自英国、荷兰、德国、瑞士和南美洲的多个马铃薯白线虫群体之间的关系。所有群体的扩增产物均为大小相似的1150 bp片段。用多种限制性内切酶对扩增片段进行酶切,结果显示群体之间存在差异。限制性内切酶RsaI区分出的群体最多。该酶揭示的RFLP模式很复杂,可能源于群体内个体之间的异质性以及个体重复序列之间的差异。对六个群体进行序列分析,并结合对PCR产物的RFLP分析,结果表明马铃薯白线虫的rDNA存在种内变异。