Detection of heterogeneity of 18S rRNA inter-genes and mutation arising during PCR amplification.

K Ueda, K Mikata
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Abstract

Direct sequencing revealed sequence heterogeneity among ribosomal RNA gene (rDNA) operons, consisting of 8 base heterogeneous sites on the 18S rDNA of Galactomyces citri-aurantii IFO 10822, and 6 base heterogeneous sites in the same region on the 18S rDNA of G. citri-aurantii IFO 10821. Sequence analysis of the cloned 18S rRNA genes of 14 species (19 strains) of ascomycetous yeast-like fungi detected a total of 32 substitutions between two cloned sequences from each of 10 strains. Eight substitutions came from heterogeneity of G. citri-aurantii IFO 10822, and 24 substitutions were predicted to be due to misincorporation by the Taq DNA polymerase. A low frequency of random substitution, estimated to occur in PCR at approximately 1 in 2690 nucleotides, was detected; and transitions occurred 7 times more frequently than transversions.

18S rRNA间基因异质性检测及PCR扩增过程中产生的突变。
直接测序结果显示,核糖体RNA基因(rDNA)操纵子序列存在异质性,其中柑橘金酸半乳糖(Galactomyces citri-aurantii IFO 10822)的18S rDNA上存在8个碱基异质位点,而柑橘金酸半乳糖(G. citri-aurantii IFO 10821)的18S rDNA上存在6个相同区域的碱基异质位点。对14种(19株)子囊菌类酵母样真菌克隆的18S rRNA基因进行序列分析,发现10株中每株克隆的两个序列之间共有32个替换。8个取代来自G. citri-aurantii IFO 10822的异质性,24个取代来自Taq DNA聚合酶的误结合。检测到低频率的随机替换,估计在2690个核苷酸中约有1个发生在PCR中;转变的发生频率是颠倒的7倍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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