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属的分子系统学:核糖体DNA限制性多态性分析

Molecular systematics of the genus analysis of restriction polymorphisms in ribosomal DNA.

作者信息

Béatrice Lraçabal, Georgios Zervakis

机构信息

Laboratoire de Génétique Moléculaire et d'Amélioration des Champignons Cultivés, Université de Bordeaux II -INRA, CRA de Bordeaux, BP 81, 33883 Villenave d'Ornon Cedex, France.

出版信息

Microbiology (Reading). 1995 Jun;141(6):1479-1490. doi: 10.1099/13500872-141-6-1479.

Abstract

Part of the nuclear ribosomal DNA unit of , including most of the intergenic sequences, was used as a probe to hybridize with DNA from eleven taxa (29 isolates), digested with nine restriction endonucleases. For all digests, a high level of rDNA heterogeneity between and within species was detected, which is in agreement with the phenetic variability already reported in previous studies on taxa. Numerical analysis of the results, performed by use of two different tree-making methods, clearly distinguished among well-defined species, i.e. and , which presented large phenetic distances with the rest of the taxa tested. , despite morphological similarity and interfertility with , appears to be a discrete taxon. Although they showed relative affinity, and presented large distances among their representative isolates, supporting the idea that they correspond to distinct taxa. All strains of and having small phenetic distances were closely positioned on dendrograms; in relation to results from recent interfertility and isozyme studies, these results support the common genetic background of and ; the position of remains controversial. Furthermore, the rDNA analysis identified ten fragments suitable for species identification: eight allowed the characterization of five taxa ( and ) and two distinguished among clusters including related taxa. By a combination of just two restriction enzymes, the rDNA probe used seems to be the appropriate tool for both varietal characterization and protection of commercially valuable strains.

摘要

(文中提及的某个物种)核糖体DNA单位的一部分,包括大部分基因间序列,被用作探针与11个分类单元(29个分离株)的DNA杂交,这些DNA用9种限制性内切酶进行了消化。对于所有消化产物,在物种间和物种内均检测到高水平的rDNA异质性,这与先前关于该分类单元的研究中已报道的表型变异性一致。通过使用两种不同的建树方法对结果进行数值分析,能够清楚地区分明确界定的物种,即(物种名1)和(物种名2),它们与所测试的其他分类单元呈现出较大的表型距离。(物种名3)尽管与(物种名4)形态相似且可育,但似乎是一个独立的分类单元。虽然它们显示出相对的亲缘关系,但(物种名5)和(物种名6)在其代表性分离株之间呈现出较大距离,支持了它们对应不同分类单元的观点。所有表型距离较小的(物种名7)和(物种名8)菌株在系统发育树上紧密相邻;结合近期可育性和同工酶研究的结果,这些结果支持了(物种名7)和(物种名8)的共同遗传背景;(物种名9)的位置仍存在争议。此外,rDNA分析确定了10个适合物种鉴定的片段:其中8个可用于鉴定5个分类单元(和),另外2个可区分包括相关分类单元的聚类。仅通过两种限制性内切酶的组合,所使用的rDNA探针似乎是用于品种鉴定和保护商业上有价值菌株的合适工具。

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