Tsuge T, Kobayashi H, Nishimura S
Faculty of Agriculture, Nagoya University, Japan.
Curr Genet. 1989 Oct;16(4):267-72. doi: 10.1007/BF00422113.
DNA encoding ribosomal RNA (rRNA) of Alternaria alternata Japanese pear pathotype has been cloned in lambda replacement vector, lambda Fix. Restriction endonuclease mapping and Southern hybridization with the 18S and 28S rRNAs of Saccharomyces cerevisiae revealed the A. alternata rDNA to be tandemly repeating 8.15-kilobase pair unit. The restriction fragments of the unit were then subcloned in the plasmid vector Bluescribe M13- and partially sequenced. The determined sequences were compared with previously reported sequences of S. cerevisiae rRNAs and their genes. The locations of DNA sequences encoding the 5.8S, 18S, and 28S rRNAs were determined by homology search using reported sequences. The complete DNA sequence for 5.8S rRNA of the fungus was found to be highly conserved at more than 90% homology in the fungi analyzed. However, sequence diversities were observed in limited regions involved in a helix structure, the helix (e), found at position 116-137.
编码链格孢日本梨致病型核糖体RNA(rRNA)的DNA已被克隆到λ置换载体λFix中。用酿酒酵母的18S和28S rRNA进行限制性内切酶图谱分析和Southern杂交,结果表明链格孢rDNA是以8.15千碱基对单位串联重复的。然后将该单位的限制性片段亚克隆到质粒载体Bluescribe M13 - 中并进行部分测序。将测定的序列与先前报道的酿酒酵母rRNA及其基因序列进行比较。通过使用报道的序列进行同源性搜索,确定了编码5.8S、18S和28S rRNA的DNA序列的位置。发现该真菌5.8S rRNA的完整DNA序列在分析的真菌中具有超过90%的同源性,高度保守。然而,在涉及位于116 - 137位的螺旋结构(螺旋(e))的有限区域中观察到序列多样性。