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首页> 外文期刊>Journal of Molecular Biology >LEADING STRAND SPECIFIC SPONTANEOUS MUTATION CORRECTS A QUASIPALINDROME BY AN INTERMOLECULAR STRAND SWITCH MECHANISM
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LEADING STRAND SPECIFIC SPONTANEOUS MUTATION CORRECTS A QUASIPALINDROME BY AN INTERMOLECULAR STRAND SWITCH MECHANISM

机译:主导的特定自发突变通过分子间的开关机制纠正了准LIN回

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imperfect inverted repeats or quasipalindromes can undergo spontaneous, often complex mutational events that correct them to perfect palindromes. Two models that depend on the quasipalindrome providing a template for a specific mutational event have been described to explain this mutation: an intramolecular anal an intermolecular strand switch model. A 17bp quasipalindrome containing a -1 deletion within the chloramphenicol acetyl transferase (CAT) gene in plasmid pJT7 undergoes a spontaneous +1 frameshift mutation that creates a perfect inverted repeat and a Cm-r phenotype. By analyzing this mutation frequency in two plasmids that contain the CAT gene in either orientation with respect to the origin of replication, we show that the specific frameshift occurs preferentially in the leading strand during DNA replication. Due to the availability and proximity of the lagging strand template as a single strand during replication of the quasipalindrome in the leading but not lagging strand, we suggest that the specificity for the leading strand correction is due to a leading strand specific intermolecular strand switch rather than an intramolecular strand switch. To test this hypothesis, we have designed a genetic selection to detect a leading strand intermolecular strand switch. This selection utilizes asymmetric quasipalindromes, one of which contains tw central stop codons. When cloned into the CAT gene in pJT7, reversion to Cm-r requires inversion of the stop codons and addition of a +1 frameshift to correct the reading frame. The inversion of the central stop codons, which is predicted by an intermolecular but not an intramolecular strand switch, occurs concomitant with the specific correction of the original 17 bp quasipalindrome. Inversion of an asymmetric center can also be demonstrated when not under selective pressure using a quasipalindrome lacking central stop codons. These results are consistent with the correction of a quasipalindrome occurring predominantly by an intermolecular strand switch during replication of the leading strand. (C) 1997 Academic Press Limited. [References: 37]
机译:不完美的反向重复序列或准回文可能会发生自发的,通常是复杂的突变事件,从而将其纠正为完美的回文。已经描述了两种依赖准古菌种的模型来提供特定突变事件的模板来解释这种突变:分子内肛门分子间链转换模型。质粒pJT7中的氯霉素乙酰转移酶(CAT)基因中含有-1缺失的17bp准回文体经历了自发的+1移码突变,产生了完美的反向重复和Cm-r表型。通过分析两个相对于复制起点在任一方向上都包含CAT基因的质粒中的这种突变频率,我们显示出特定的移码优先发生在DNA复制过程中的前导链中。由于在前主链而非拟链的准palindrome的复制过程中,后支链模板作为单链的可用性和接近性,我们建议前导链校正的特异性是由于前导链特异性分子间链切换而不是分子内链开关。为了验证该假设,我们设计了一种基因选择方法来检测前导链分子间链开关。这种选择利用了不对称的准回文,其中一个包含两个中央终止密码子。当克隆到pJT7的CAT基因中时,回复到Cm-r需要反转终止密码子并加上+1移码以校正阅读框。中心终止密码子的倒转是由分子间而不是分子内的链开关预测的,与原始17 bp准palindrome的特定校正同时发生。当不使用缺乏中心终止密码子的准回文蝇在选择性压力下不对称中心也可以被反转。这些结果与在前导链的复制过程中主要通过分子间链转换发生的准回文的校正是一致的。 (C)1997 Academic Press Limited。 [参考:37]

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