Pramateftaki P V, Antoniou P P, Typas M A
Department of Genetics and Biotechnology, Faculty of Biology, University of Athens, Panepistimiopolis, Athens, 15701, Greece.
Fungal Genet Biol. 2000 Feb;29(1):19-27. doi: 10.1006/fgbi.1999.1178.
The complete DNA sequence of the nuclear ribosomal RNA gene complex of Verticillium dahliae: Intraspecific heterogeneity within the intergenic spacer region. Fungal Genetics and Biology 29, 19-27. The complete sequence of the nuclear ribosomal DNA gene complex of the phytopathogenic fungus Verticillium dahliae has been determined. The tandemly repeated unit was 7216 bp long and appears to be the shortest rDNA cluster described so far among filamentous fungi. Primer pairs were designed for amplification of the region spanning half of the 28S subunit, the intergenic spacer (IGS), and the 5' end of 18S subunit of a number of Verticillium strains, isolated from various hosts and geographic origins. Great heterogeneity was detected in the amplified products of the IGS region resulting in fragments varying from 1.6 to 2.0 kb. The majority of Verticillium isolates were classified into two groups with 1.6- and 1.7-kb amplified products, respectively. The former group included 31 V. dahliae, 7 V. longisporum, and 1 V. albo-atrum isolates, whereas the latter included 10 V. dahliae and 1 V. albo-atrum isolates. Sequence analysis of representative PCR products of the above groups identified a "hot-spot" region harboring most of larger insertions, whereas most of the small changes were due to transitions and transversions. One V. longisporum isolate with a 2.0-kb PCR product contained 13 perfectly conserved tandem repeats of 39 bp long. The presence of similar incomplete sequences in the corresponding regions of V. dahliae, V. longisporum, and V. albo-atrum isolates revealed a particular standard motif of insertions in the IGS region of the genus and is discussed.
大丽轮枝菌核糖体RNA基因复合体的完整DNA序列:基因间隔区的种内异质性。《真菌遗传学与生物学》29卷,19 - 27页。已测定了植物病原真菌大丽轮枝菌核糖体DNA基因复合体的完整序列。串联重复单元长7216 bp,似乎是迄今为止在丝状真菌中描述的最短的核糖体DNA簇。设计了引物对,用于扩增从多种寄主和地理来源分离的多个大丽轮枝菌菌株的28S亚基一半、基因间隔区(IGS)和18S亚基5′端的区域。在IGS区域的扩增产物中检测到很大的异质性,产生的片段长度从1.6 kb到2.0 kb不等。大多数大丽轮枝菌分离株分别被分为两组,扩增产物长度分别为1.6 kb和1.7 kb。前一组包括31株大丽轮枝菌、7株长孢轮枝菌和1株黑白轮枝菌分离株,而后一组包括10株大丽轮枝菌和1株黑白轮枝菌分离株。对上述两组代表性PCR产物的序列分析确定了一个“热点”区域,该区域含有大多数较大的插入片段,而大多数小的变化是由于转换和颠换。一株长孢轮枝菌分离株的PCR产物为2.0 kb,其中包含13个39 bp长的完全保守串联重复序列。在大丽轮枝菌、长孢轮枝菌和黑白轮枝菌分离株的相应区域中存在相似但不完整的序列,揭示了该属IGS区域插入的一个特定标准基序,并对此进行了讨论。