密歇根樱桃蒙利菌与松拉蒙利菌的遗传变异

C. Snyder, A. Jones
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引用次数: 39

摘要

摘要利用聚合酶链反应(PCR)技术对美国密歇根果园产的果假单胞菌(Monilinia fructicola)和散假单胞菌(Monilinia laxa)分离株的rDNA进行分析,揭示了其内部转录间隔区1 (ITSI)限制性位点的变异和小亚单位(SSU) rRNA基因长度的变异。两种的1TS1序列长度均为146;但在3个位置上,松果霉的ITSI与松果霉的ITSI存在差异。虽然这两个物种的ITS1区域序列几乎相同,但tilrel酶切割pcr扩增的ITSI区域是不同的。对SSU rRNA基因的3′端进行PCR扩增,分别从果霉和laxa中得到约940和520个产物。在32株果实分枝杆菌的SSU rDNA中检测到一个421 bp的I族内含子,而在8株laxa分枝杆菌中未检测到该内含子。四个分离株的内含子序列相同,SSU rDNA侧翼序列相同。
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Genetic variation between strains of Monilinia fructicola and Monilinia laxa isolated from cherries in Michigan
Abstract Polymerase chain reaction (PCR)-mediated analysis of rDNA from isolates of Monilinia fructicola and Monilinia laxa from Michigan cheny orchards revealed interspecies restriction site variation in the internal transcribed spacer 1 (ITSI) region and length variation in the small subunit (SSU) rRNA gene. 1TS1 sequences from both species were 146 by long; however, the ITSI of M. laxa differed at three positions from the ITSI of M. fructicola. Although the sequences of the ITS1 regions from both species were nearly identical, the enzyme tilrel cuts the PCR-amplified ITSI region of the two species differentially. PCR amplification of the 3′ end of the SSU rRNA gene yielded products of approximately 940 and 520 by from M. fructicola and M. laxa, respectively. A 421-bp group I intron was detected by PCR within the SSU rDNA of 32 isolates of M. fructicola but not in the eight isolates of M. laxa. Intron sequences from each of four isolates of M. fructicola were identical, and the SSU rDNA flanking sequenc...
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