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DNA sequences required to induce localized conversion in Streptococcus pneumoniae transformation.

作者信息

Garcia P, Gasc A M, Kyriakidis X, Baty D, Sicard M

机构信息

Centre de Recherche de Biochimie et Génétique Cellulaires du C.N.R.S., Toulouse, France.

出版信息

Mol Gen Genet. 1988 Nov;214(3):509-13. doi: 10.1007/BF00330488.

DOI:10.1007/BF00330488
PMID:3216856
Abstract

In pneumococcal transformation a particular point mutation belonging to the amiA locus is able markedly to enhance recombination frequency when crossed with any other markers of this gene. This results from a polarized conversion of the mutation towards the wild-type sequence. In this report, by site-directed oligonucleotide mutagenesis, we have generated a series of mutants showing various degrees of conversion. We have found that the substitution 5'-ATTCAT----5'-ATTAAT is a sufficient signal for localized conversion. Changing individual bases within this sequence results in decreased conversion frequencies to levels that depend on the mutation, suggesting that there is a family to related sequences which may act as a substrate for a conversion system. Moreover, the length over which this conversion occurs has been estimated to be 12 base pairs on the average.

摘要

相似文献

1
DNA sequences required to induce localized conversion in Streptococcus pneumoniae transformation.
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2
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本文引用的文献

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Rapid cloning of specific DNA fragments of Streptococcus pneumoniae by vector integration into the chromosome followed by endonucleolytic excision.通过载体整合到染色体中,随后进行核酸内切酶切除来快速克隆肺炎链球菌的特定DNA片段。
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Excision and repair of mismatched base pairs in transformation of Streptococcus pneumoniae.肺炎链球菌转化过程中错配碱基对的切除与修复
Mol Gen Genet. 1980 Apr;178(1):191-201. doi: 10.1007/BF00267229.
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Oligonucleotide-directed mutagenesis using M13-derived vectors: an efficient and general procedure for the production of point mutations in any fragment of DNA.
体内T:G错配的极短片段修复:背景和辅助蛋白的重要性
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使用M13衍生载体的寡核苷酸定向诱变:在任何DNA片段中产生点突变的高效通用方法。
Nucleic Acids Res. 1982 Oct 25;10(20):6487-500. doi: 10.1093/nar/10.20.6487.
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Cloning of Streptococcus pneumoniae DNA: its use in pneumococcal transformation and in studies of mismatch repair.肺炎链球菌DNA的克隆:其在肺炎球菌转化及错配修复研究中的应用
Gene. 1981 Jan-Feb;13(1):65-73. doi: 10.1016/0378-1119(81)90044-5.
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Evolution of immunoglobulin V genes: evidence indicating that recently duplicated human V kappa sequences have diverged by gene conversion.免疫球蛋白V基因的进化:证据表明最近复制的人类Vκ序列已通过基因转换发生分歧。
Cell. 1983 Jan;32(1):181-9. doi: 10.1016/0092-8674(83)90508-1.
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A novel repair enzyme: UVRABC excision nuclease of Escherichia coli cuts a DNA strand on both sides of the damaged region.一种新型修复酶:大肠杆菌的UVRABC切除核酸酶在受损区域两侧切割DNA链。
Cell. 1983 May;33(1):249-60. doi: 10.1016/0092-8674(83)90354-9.
7
Mismatch repair in Streptococcus pneumoniae: relationship between base mismatches and transformation efficiencies.肺炎链球菌中的错配修复:碱基错配与转化效率之间的关系。
Proc Natl Acad Sci U S A. 1983 Oct;80(19):5956-60. doi: 10.1073/pnas.80.19.5956.
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Efficient site-directed mutagenesis by simultaneous use of two primers.通过同时使用两种引物进行高效的定点诱变。
Nucleic Acids Res. 1983 Aug 11;11(15):5103-12. doi: 10.1093/nar/11.15.5103.
9
Transformation of Streptococcus pneumoniae with S. pneumoniae-lambda phage hybrid DNA: induction of deletions.用肺炎链球菌-λ噬菌体杂交DNA对肺炎链球菌进行转化:缺失的诱导
Proc Natl Acad Sci U S A. 1980 Jun;77(6):3534-8. doi: 10.1073/pnas.77.6.3534.
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The gapped duplex DNA approach to oligonucleotide-directed mutation construction.用于寡核苷酸定向突变构建的缺口双链DNA方法。
Nucleic Acids Res. 1984 Dec 21;12(24):9441-56. doi: 10.1093/nar/12.24.9441.