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Majority of divergence between closely related DNA samples is due to indels

机译:密切相关的DNA样本之间的大部分差异是由于indels

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摘要

It was recently shown that indels are responsible for more than twice as many unmatched nucleotides as are base substitutions between samples of chimpanzee and human DNA. A larger sample has now been examined and the result is similar. The number of indels is approximate to1/12th of the number of base substitutions and the average length of the indels is 36 nt, including indels up to 10 kb. The ratio (R-u) of unpaired nucleotides attributable to indels to those attributable to substitutions is 3.0 for this 2 million-nt chimp DNA sample compared with human. There is similar evidence of a large value of R-u for sea urchins from the polymorphism of a sample of Strongylocentrotus purpuratus DNA (Ru = 3-4). Other work indicates that similarly, per nucleotide affected, large differences are seen for indels in the DNA polymorphism of the plant Arabidopsis thaliana (R-u = 51). For the insect Drosophila melanogaster a high value of R-u (4.5) has been determined. For the nematode Caenorhabditis elegans the polymorphism data are incomplete but high values of R-u are likely. Comparison of two strains of Escherichia coli O157:H7 shows a preponderance of indels. Because these six examples are from very distant systematic groups the implication is that in general, for alignments of closely related DNA, indels are responsible for many more unmatched nucleotides than are base substitutions. Human genetic evidence suggests that indels are a major source of gene defects, indicating that indels are a significant source of evolutionary change.
机译:最近显示,与黑猩猩和人类DNA样本之间的碱基取代相比,插入缺失所引起的不匹配核苷酸数量要多两倍。现在已经检查了更大的样本,结果相似。插入缺失的数目约为碱基取代数目的1/12,并且插入缺失的平均长度为36nt,包括高达10kb的插入缺失。与人类相比,这个200万核苷酸的黑猩猩DNA样品中,插入缺失的非配对核苷酸与置换引起的非配对核苷酸的比例(R-u)为3.0。有类似的证据表明,从紫背天牛(Stryylocentrotus purpuratus)DNA(Ru = 3-4)样本的多态性来看,R-u对于海胆具有很大的价值。其他工作表明,类似地,每受影响的核苷酸,植物拟南芥DNA多态性中的插入缺失存在较大差异(R-u = 51)。对于昆虫果蝇(Drosophila melanogaster),已确定了较高的R-u(4.5)。对于线虫秀丽隐杆线虫,多态性数据不完整,但R-u值可能很高。两种大肠杆菌O157:H7菌株的比较显示出大量的插入缺失。因为这六个例子来自非常遥远的系统群体,所以这意味着通常来说,对于紧密相关的DNA的比对,插入缺失与碱基取代相比,负责更多的不匹配核苷酸。人类遗传学证据表明,插入缺失是基因缺陷的主要来源,表明插入缺失是进化变化的重要来源。

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