Osakabe M, Hinomoto N, Toda S, Komazaki S, Goka K
Department of Plant Protection, National Agriculture Research Center, Tsukuba, Ibaraki, Japan.
Exp Appl Acarol. 2000;24(5-6):385-95. doi: 10.1023/a:1006405325992.
Genetic markers were searched using PCR with 40 kinds of decanucleotide primers to investigate DNA polymorphism in Panonychus citri. A region consisting of a variable number of CT tandem repeats (microsatellite) was found in a fragment amplified with the OPB10 primer. The microsatellite differed in size by ca. 100bp among several P. citri populations screened and was derived from at least seven alleles. This region was characteristic of P. mori and P. osmanthi, but was lacking in P. ulmi. The flanking regions were highly conserved among these species.
使用40种十聚体引物通过聚合酶链反应(PCR)寻找遗传标记,以研究柑橘全爪螨的DNA多态性。在用OPB10引物扩增的片段中发现了一个由可变数量的CT串联重复序列(微卫星)组成的区域。在筛选的几个柑橘全爪螨种群中,该微卫星的大小相差约100bp,并且至少来自七个等位基因。该区域是家蚕和桑白盾蚧的特征,但在榆全爪螨中不存在。这些物种的侧翼区域高度保守。