Mayo Clinic College of Medicine, Rochester, MN 55905, USA.
Nucleic Acids Res. 2010 Mar;38(5):1575-82. doi: 10.1093/nar/gkp1119. Epub 2009 Dec 9.
The rate of mutation refers to the probability that a unit length of DNA (generally a base pair) mutates with time. Fluctuation analysis or mutant accumulation assays applied to phenotypic changes measure mutation rates of cells. However, only a few phenotypic changes indicative of mutations are known thus limiting the analysis to those rare genes. Direct sequencing overcomes the limitations imposed by phenotypic analysis but is limited by the extensive number of clones or cells that have to be analyzed in fluctuation or mutant accumulation assays. We propose a strategy to determine the rate of mutation of a gene by limited direct sequencing of a few single cells of a defined lineage. To accomplish this, we determined the average number of mutations per position in each DNA length sequenced from the proportion of the non-mutated positions, according to the Poisson process and/or the Taylor series. Measuring the rate of mutation by direct sequencing of genes does not require ascertaining a phenotype and can be applied to any area of the genome in a cell. The approach avoids fluctuation errors.
突变率是指单位长度的 DNA(通常为碱基对)随时间发生突变的概率。应用于表型变化的波动分析或突变体积累测定法来测量细胞的突变率。然而,只有少数能够指示突变的表型变化是已知的,这限制了对那些罕见基因的分析。直接测序克服了表型分析的局限性,但受到波动或突变体积累测定法中必须分析的大量克隆或细胞的限制。我们提出了一种通过对特定谱系的少数几个单细胞进行有限的直接测序来确定基因突变率的策略。为此,我们根据泊松过程和/或泰勒级数,从测序的 DNA 长度中未突变位置的比例来确定每个位置的平均突变数。通过直接测序基因来测量突变率不需要确定表型,可以应用于细胞中基因组的任何区域。该方法避免了波动误差。