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首页> 外文期刊>Microbiological Research >Differentiation of homokaryons and heterokaryons of Agaricus bisporus with inter-simple sequence repeat markers
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Differentiation of homokaryons and heterokaryons of Agaricus bisporus with inter-simple sequence repeat markers

机译:利用简单序列重复标记区分双孢蘑菇的同核和异核

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Morphologically different fifteen slow growing single spore isolates (SSIs) were screened from germinated basidiospores of Agaricus bisporus; assumed to be homokaryons, and subjected to growth rate, spawn run, fruiting and inter-simple sequence repeat (ISSR) analysis for confirmation of true homokaryons. The present studies are the first report of fingerprinting on differentiating homo- and heterokaryotic SSIs using ISSR markers. The patterns were highly polymorphic and very reproducible. Among 40 primers tested, 7 ISSR primers were selected for the analysis of genomic DNA and generated a total of 54 ISSR fragments, sufficient to differentiate the 15 isolates from each other. ISSR fingerprinting detected 46.30% polymorphic loci. All appressed homokaryons carried a subset of ISSR markers found in the heterokaryons, and these were not able to produce a fruiting body. A test of cross-fertility and the following fruiting trial proved that 3 of the 15 SS's with different ISSR fingerprints were homokaryons. None of the discarded SSIs have any missing bands present in the parental heterokaryotic control; these are heterokaryons derived from non-sister nuclear pairs. It is revealed that homokaryons are probably restricted to the assumed morphological classes of SSIs. These results demonstrate that ISSR markers provide an efficient alternate for identification of homokaryons and suggest these markers be considered as new tools for the survey of Agaricus species
机译:从双孢蘑菇的萌发的担子孢子中筛选形态不同的十五个缓慢生长的单孢子分离株(SSIs)。假定为同核体,并经过生长速率,产卵运行,结果和简单序列间重复(ISSR)分析,以确认真正的同核体。本研究是使用ISSR标记区分同核和异核SSI的指纹图谱的首次报道。这些模式是高度多态的,并且非常可重复。在测试的40个引物中,选择了7个ISSR引物用于基因组DNA分析,并产生了总共54个ISSR片段,足以区分15个分离株。 ISSR指纹检测到46.30%的多态位点。所有贴附的同核核糖核酸都带有在异核核糖核酸中发现的一部分ISSR标记,这些标记不能产生子实体。一项交叉育性测试和随后的结果试验证明,具有不同ISSR指纹的15个SS中有3个是纯核体。丢弃的SSI均未在亲代异核生物对照中存在任何缺失带。这些是源自非姐妹核对的异核。据揭示,同核体可能仅限于假定的SSI形态学类别。这些结果表明,ISSR标记为鉴定同核生物提供了一种有效的替代方法,并表明这些标记被认为是姬松茸属物种调查的新工具。

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