Glickman B W, Ripley L S
Proc Natl Acad Sci U S A. 1984 Jan;81(2):512-6. doi: 10.1073/pnas.81.2.512.
A model is presented for deletion mutations whose formation is mediated by palindromic and quasipalindromic DNA sequences. It proposes that the self-complementarity of palindromes allows the formation of DNA secondary structures that serve as deletion intermediates. The structures juxtapose the end points of the deletion and thus direct deletion specificity. While misaligned DNA intermediates that explain deletion termini occurring in repeated DNA sequences have been described, no explanations have been offered for deletion termini occurring in other sequences. The DNA secondary structures whose formation is mediated by palindromic sequences appear to explain many of these. In this paper, secondary-structure intermediates are described for a series of spontaneous deletions of known sequence in the lacl gene of Escherichia coli. The model is supported by its failure to predict structures that can juxtapose simulated deletion termini in the lacl gene. We have found a strong association between palindromic sequences and repeated sequences at lacl deletion termini that suggests the joint participation of repeated and palindromic DNA sequences in the formation of some deletions. Sequences of deletions in other organisms also suggest the participation of palindromic DNA sequences in the formation of deletions.
本文提出了一种由回文和类回文DNA序列介导形成的缺失突变模型。该模型认为,回文序列的自我互补性允许形成作为缺失中间体的DNA二级结构。这些结构使缺失的端点并列,从而决定缺失特异性。虽然已经描述了能解释重复DNA序列中出现的缺失末端的错配DNA中间体,但对于其他序列中出现的缺失末端却没有给出解释。由回文序列介导形成的DNA二级结构似乎可以解释其中许多情况。本文描述了大肠杆菌lacl基因中一系列已知序列的自发缺失的二级结构中间体。该模型因未能预测出能使lacl基因中模拟缺失末端并列的结构而得到支持。我们发现lacl缺失末端的回文序列与重复序列之间存在很强的关联,这表明重复和回文DNA序列共同参与了某些缺失的形成。其他生物体中的缺失序列也表明回文DNA序列参与了缺失的形成。