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Achilles' heel cleavage: creation of rare restriction sites in lambda phage genomes and evaluation of additional operators, repressors and restriction/modification systems.

作者信息

Grimes E, Koob M, Szybalski W

机构信息

McArdle Laboratory for Cancer Research, University of Wisconsin, Madison 53706.

出版信息

Gene. 1990 May 31;90(1):1-7. doi: 10.1016/0378-1119(90)90432-q.

DOI:10.1016/0378-1119(90)90432-q
PMID:2165969
Abstract

A novel technique for the creation of rare restriction sites was described by Koob et al. [Science 241 (1988) 1084-1086]. This technique, Achilles' heel cleavage (AC), relies on the use of a bound repressor molecule to protect only one of many identical restriction sites from a modification methyltransferase that inactivates all other restriction sites. The technique was applied to a small plasmid and shown to work efficiently with two repressor/operator systems: lac repressor/lacO operator and lambda repressor/lambda oL1 operator. Here, we have extended these results to a lac operator carried by a much larger vector, namely a 44-kb phage lambda construct. In addition, we have evaluated the effect of altering the stability of the lac repressor/lac operator complex by varying both the operator and the repressor. We have also evaluated several more restriction/modification systems (MboI, Dam, MspI and AluI) in addition to HhaI and HaeII used earlier. Finally, we extended the AC technique to a third system, that of the phage 434 repressor and a synthetic 434 operator. From our results we conclude that the AC method should be applicable to the mapping of large genomes and to measuring the strength of operator-repressor interactions. AC could also be applied to identifying and evaluating many different DNA-binding proteins and their sites of action.

摘要

相似文献

1
Achilles' heel cleavage: creation of rare restriction sites in lambda phage genomes and evaluation of additional operators, repressors and restriction/modification systems.
Gene. 1990 May 31;90(1):1-7. doi: 10.1016/0378-1119(90)90432-q.
2
Conferring operator specificity on restriction endonucleases.
Science. 1988 Aug 26;241(4869):1084-6. doi: 10.1126/science.2842862.
3
DNA sequence dependent and independent conformational changes in multipartite operator recognition by lambda-repressor.λ阻遏蛋白对多部分操纵子识别过程中依赖和不依赖DNA序列的构象变化
Biochemistry. 2000 Mar 28;39(12):3377-83. doi: 10.1021/bi9919955.
4
Lac repressor with the helix-turn-helix motif of lambda cro binds to lac operator.带有λ噬菌体cro蛋白螺旋-转角-螺旋基序的乳糖阻遏蛋白与乳糖操纵基因结合。
EMBO J. 1992 Aug;11(8):3031-8. doi: 10.1002/j.1460-2075.1992.tb05373.x.
5
A novel method for converting common restriction enzymes into rare cutters: integration host factor-mediated Achilles' cleavage (IHF-AC).一种将常用限制酶转化为稀有切割酶的新方法:整合宿主因子介导的阿喀琉斯切割(IHF-AC)。
Gene. 1992 Jan 2;110(1):1-7. doi: 10.1016/0378-1119(92)90437-t.
6
How Lac repressor finds lac operator in vitro.乳糖阻遏蛋白在体外如何找到乳糖操纵基因。
J Mol Biol. 1992 Jul 5;226(1):59-68. doi: 10.1016/0022-2836(92)90124-3.
7
The interaction of the recognition helix of lac repressor with lac operator.乳糖阻遏蛋白的识别螺旋与乳糖操纵基因的相互作用。
EMBO J. 1987 Oct;6(10):3145-53. doi: 10.1002/j.1460-2075.1987.tb02625.x.
8
DNA recognition by the helix-turn-helix motif: investigation by laser Raman spectroscopy of the phage lambda repressor and its interaction with operator sites OL1 and OR3.通过螺旋-转角-螺旋基序进行的DNA识别:利用激光拉曼光谱对噬菌体λ阻遏物及其与操纵子位点OL1和OR3的相互作用进行研究。
Biochemistry. 1991 Jun 18;30(24):5955-63. doi: 10.1021/bi00238a020.
9
Lac repressor - lac operator interaction. Circular dichroism study.乳糖阻遏蛋白-乳糖操纵基因相互作用。圆二色性研究。
Nucleic Acids Res. 1981 Oct 10;9(19):5175-84. doi: 10.1093/nar/9.19.5175.
10
NMR studies of DNA recognition sequences and their interaction with proteins. The phage lambda OR1 operator, a symmetric lac operator and their specific complexes with cro protein and lac repressor "headpiece".DNA识别序列及其与蛋白质相互作用的核磁共振研究。噬菌体λ OR1操纵子、对称的乳糖操纵子及其与cro蛋白和乳糖阻遏物“头部”的特异性复合物。
J Biomol Struct Dyn. 1986 Apr;3(5):899-911. doi: 10.1080/07391102.1986.10508472.

引用本文的文献

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J Bacteriol. 2010 Feb;192(4):1113-21. doi: 10.1128/JB.01515-09. Epub 2009 Dec 18.
2
Neomycin- and hygromycin-resistance expression cassettes containing an artificial triple-helix site and a synthetic lac operator facilitate restriction endonuclease cleavage at pre-defined sites and recovery of specific fragments from mammalian genomes.含有人工三链螺旋位点和合成乳糖操纵子的新霉素和潮霉素抗性表达盒有助于在预定义位点进行限制性内切酶切割,并从哺乳动物基因组中回收特定片段。
Mamm Genome. 1994 Mar;5(3):183-6. doi: 10.1007/BF00352354.
3
RecA-AC: single-site cleavage of plasmids and chromosomes at any predetermined restriction site.
RecA-AC:在任何预定的限制位点对质粒和染色体进行单一位点切割。
Nucleic Acids Res. 1992 Nov 11;20(21):5831-6. doi: 10.1093/nar/20.21.5831.