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AvaI和BsoBI限制-修饰系统的克隆与序列比较

Cloning and sequence comparison of AvaI and BsoBI restriction-modification systems.

作者信息

Ruan H, Lunnen K D, Scott M E, Moran L S, Slatko B E, Pelletier J J, Hess E J, Benner J, Wilson G G, Xu S Y

机构信息

New England Biolabs, Inc., Beverly, MA 01915, USA.

出版信息

Mol Gen Genet. 1996 Oct 28;252(6):695-9.

PMID:8917312
Abstract

AvaI and BsoBI restriction endonucleases are isoschizomers which recognize the symmetric sequence 5'CYCGRG3' and cleave between the first C and second Y to generate a four-base 5' extension. The AvaI restriction endonuclease gene (avaIR) and methylase gene (avaIM) were cloned into Escherichia coli by the methylase selection method. The BsoBI restriction endonuclease gene (bsoBIR) and part of the BsoBI methylase gene (bsoBIM) were cloned by the "endo-blue" method (SOS induction assay), and the remainder of bsoBIM was cloned by inverse PCR. The nucleotide sequences of the two restriction-modification (RM) systems were determined. Comparisons of the predicted amino acid sequences indicated that AvaI and BsoBI endonucleases share 55% identity, whereas the two methylases share 41% identity. Although the two systems show similarity in protein sequence, their gene organization differs. The avaIM gene precedes avaIR in the AvaI RM system, while the bsoBI R gene is located upstream of bsoBI M in the BsoBI RM system. Both AvaI and BsoBI methylases contain motifs conserved among the N4 cytosine methylases.

摘要

AvaI和BsoBI限制性内切酶是同裂酶,它们识别对称序列5'CYCGRG3',并在第一个C和第二个Y之间切割,产生一个四碱基的5'端延伸。通过甲基化酶选择法将AvaI限制性内切酶基因(avaIR)和甲基化酶基因(avaIM)克隆到大肠杆菌中。通过“内切蓝”法(SOS诱导测定)克隆了BsoBI限制性内切酶基因(bsoBIR)和部分BsoBI甲基化酶基因(bsoBIM),其余的bsoBIM通过反向PCR克隆。测定了这两个限制修饰(RM)系统的核苷酸序列。预测氨基酸序列的比较表明,AvaI和BsoBI内切酶具有55%的同一性,而两种甲基化酶具有41%的同一性。尽管这两个系统在蛋白质序列上显示出相似性,但它们的基因组织不同。在AvaI RM系统中,avaIM基因位于avaIR之前,而在BsoBI RM系统中,bsoBI R基因位于bsoBI M的上游。AvaI和BsoBI甲基化酶都含有在N4胞嘧啶甲基化酶中保守的基序。

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