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腺嘌呤-胸腺嘧啶到胞嘧啶-鸟嘌呤的颠换及其通过大肠杆菌mutT和mutHLS途径的预防。

A.T----C.G transversions and their prevention by the Escherichia coli mutT and mutHLS pathways.

作者信息

Schaaper R M, Bond B I, Fowler R G

机构信息

Laboratory of Molecular Genetics, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709.

出版信息

Mol Gen Genet. 1989 Oct;219(1-2):256-62. doi: 10.1007/BF00261185.

Abstract

Escherichia coli mutT strains are strong mutators yielding only A.T----C.G transversion mutations. These are thought to result from uncorrected (or unprevented) A.G mispairings during DNA replication. We have investigated the interaction of mutT-induced replication errors with the mutHLS-encoded postreplicative mismatch repair system. By measuring mutation frequencies in both forward and reversion systems, we have demonstrated that mutTmutL and mutTmutS double mutators produce no more mutants than expected from simple additivity of the frequencies in the single mutators. We conclude that mutT-induced A.G replication errors are not recognized by the MutHLS system. On the other hand, direct measurements of mismatch repair by transfection of bacteriophage M13mp2 heteroduplex DNA as well as mutational data from strains other than muT, indicate that the MutHLS system can repair at least certain A.G mispairs. We suggest that A.G mispairs may exist in several different conformations, some of which are recognized by the MutHLS system. However, the A.G mispairs normally prevented by the mutT function are refractory to mismatch repair, indicating that they may represent a structurally distinct class.

摘要

大肠杆菌mutT菌株是强突变体,只产生A.T到C.G的颠换突变。这些突变被认为是由DNA复制过程中未校正(或未预防)的A.G错配导致的。我们研究了mutT诱导的复制错误与mutHLS编码的复制后错配修复系统之间的相互作用。通过测量正向和回复系统中的突变频率,我们证明了mutTmutL和mutTmutS双突变体产生的突变体并不比单突变体频率简单相加所预期的更多。我们得出结论,mutT诱导的A.G复制错误不能被MutHLS系统识别。另一方面,通过转染噬菌体M13mp2异源双链DNA直接测量错配修复以及来自除muT之外的菌株的突变数据表明,MutHLS系统可以修复至少某些A.G错配。我们认为A.G错配可能以几种不同的构象存在,其中一些能被MutHLS系统识别。然而,通常由mutT功能预防的A.G错配难以进行错配修复,这表明它们可能代表一种结构上不同的类型。

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