Taylor J L, Borgmann I E
National Research Council of Canada, Plant Biotechnology Institute, Saskatoon, Canada.
Mol Plant Microbe Interact. 1994 Mar-Apr;7(2):181-8. doi: 10.1094/mpmi-7-0181.
A 5,238-bp repetitive DNA element from a highly virulent isolate of Leptosphaeria maculans has been cloned and sequenced. The element is present in approximately 80 copies per haploid genome and hybridizes to every chromosome resolved by pulse field gel electrophoresis. The sequence is composed of 66% A+T and has numerous, very short, direct and inverted repeats. No RNA complementary to the element was detected in log phase cultures, and no open reading frames of significant length are present in the sequence. It has no structural similarity to other repetitive elements or significant homology to database sequences. We have designated the element LMR1. Southern blot hybridization indicated that the element is present in all isolates of L. maculans that are highly virulent to Brassica napus and B. rapa. The general structure of the element was conserved among isolates of different mating type, pathogenicity group, and geographic origin, as determined by both Southern blot analysis and primer-directed DNA amplification. LMR1 did not hybridize to DNA from weakly virulent strains of L. maculans, with the exception of one isolate. Phylogenetic analyses of restriction fragment length polymorphism and rDNA sequence indicated that the highly virulent and weakly virulent strains of L. maculans are not monophyletic. Therefore, the presence of the LMR1 element in a weakly virulent isolate may indicate that a rare transfer event has occurred. Surprisingly, the weakly virulent isolate that contains LMR1 is more pathogenic on B. napus and B. juncea than a similar isolate that lacks the element.
已克隆并测序了来自甘蓝链格孢高毒力分离株的一段5238 bp的重复DNA元件。该元件在每个单倍体基因组中约有80个拷贝,并与脉冲场凝胶电泳分离出的每条染色体杂交。该序列由66%的A+T组成,有许多非常短的正向和反向重复序列。在对数期培养物中未检测到与该元件互补的RNA,序列中也不存在显著长度的开放阅读框。它与其他重复元件没有结构相似性,与数据库序列也没有显著同源性。我们将该元件命名为LMR1。Southern杂交表明,该元件存在于所有对甘蓝型油菜和白菜型油菜具有高毒力的甘蓝链格孢分离株中。通过Southern杂交分析和引物介导的DNA扩增确定,该元件的总体结构在不同交配型、致病基团和地理来源的分离株中是保守的。LMR1除了与一个分离株杂交外,未与甘蓝链格孢弱毒菌株的DNA杂交。对限制性片段长度多态性和rDNA序列的系统发育分析表明,甘蓝链格孢的高毒力和弱毒力菌株并非单系起源。因此,弱毒力分离株中LMR1元件的存在可能表明发生了罕见的转移事件。令人惊讶的是,含有LMR1的弱毒力分离株对甘蓝型油菜和芥菜型油菜的致病性比缺乏该元件的类似分离株更强。