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Statistical modeling and analysis of the LAGLIDADG family of site-specific endonucleases and identification of an intein that encodes a site-specific endonuclease of the HNH family

机译:LAGLIDADG位点特异性内切核酸酶家族的统计模型和分析,以及编码HNH家族位点特异性内切核酸酶的内含肽的鉴定

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The LAGLIDADG and HNH families of site-specific DNA endonucleases encoded by viruses, bacteriophages as well as archaeal, eucaryotic nuclear and organellar genomes are characterized by the sequence motifs ‘LAGLIDADG' and ‘HNH', respectively. These endonucleases have been shown to occur in different environments: LAGLIDADG endonucleases are found in inteins, archaeal and group I introns and as free standing open reading frames (ORFs); HNH endonucleases occur in group I and group II introns and as ORFs. Here, statistical models (hidden Markov models, HMMs) that encompass both the conserved motifs and more variable regions of these families have been created and employed to characterize known and potential new family members. A number of new, putative LAGLIDADG and HNH endonucleases have been identified including an intein-encoded HNH sequence. Analysis of an HMM-generated multiple alignment of 130 LAGLIDADG family members and the three-dimensional structure of the I-CreI endonuclease has enabled definition of the core elements of the repeated domain (~90 residues) that is present in this family of proteins. A conserved negatively charged residue is proposed to be involved in catalysis. Phylogenetic analysis of the two families indicates a lack of exchange of endonucleases between different mobile elements (environments) and between hosts from different phylogenetic kingdoms. However, there does appear to have been considerable exchange of endonuclease domains amongst elements of the same type. Such events are suggested to be important for the formation of elements of new specficity.
机译:由病毒,噬菌体以及古细菌,真核细胞和细胞器基因组编码的定点DNA内切核酸酶的LAGLIDADG和HNH家族分别以序列基序“ LAGLIDADG”和“ HNH”为特征。这些内切核酸酶已显示在不同的环境中发生:LAGLIDADG内切核酸酶存在于内含子,古细菌和I组内含子中,并以自由开放阅读框架(ORF)的形式存在。 HNH核酸内切酶存在于I组和II组内含子中,并以ORF形式出现。在这里,已经创建了涵盖这些家族的保守基序和更多可变区域的统计模型(隐马尔可夫模型,HMM),并用于表征已知和潜在的新家族成员。已经鉴定出许多新的推定的LAGLIDADG和HNH核酸内切酶,包括内含肽编码的HNH序列。对HMM产生的130个LAGLIDADG家族成员的多重比对和I-CreI核酸内切酶的三维结构的分析,使得能够定义该蛋白家族中存在的重复结构域(约90个残基)的核心元件。建议保守的带负电荷的残基参与催化。对这两个家族的系统发育分析表明,在不同的移动元件(环境)之间以及来自不同系统发育王国的宿主之间缺乏内切核酸酶的交换。然而,似乎在相同类型的元件之间已经存在相当大的核酸内切酶结构域交换。这类事件被认为对于形成新的特异性元素很重要。

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