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Cas10 蛋白的功能和系统发育多样性。

Functional and Phylogenetic Diversity of Cas10 Proteins.

机构信息

Department of Microbiology and Cell Biology, Montana State University, Bozeman, Montana, USA.

Department of Chemistry and Biochemistry, Montana State University, Bozeman, Montana, USA.

出版信息

CRISPR J. 2023 Apr;6(2):152-162. doi: 10.1089/crispr.2022.0085. Epub 2023 Mar 13.

Abstract

Cas10 proteins are large subunits of type III CRISPR RNA (crRNA)-guided surveillance complexes, many of which have nuclease and cyclase activities. Here, we use computational and phylogenetic methods to identify and analyze 2014 Cas10 sequences from genomic and metagenomic databases. Cas10 proteins cluster into five distinct clades that mirror previously established CRISPR-Cas subtypes. Most Cas10 proteins (85.0%) have conserved polymerase active-site motifs, while HD-nuclease domains are less well conserved (36.0%). We identify Cas10 variants that are split over multiple genes or genetically fused to nucleases activated by cyclic nucleotides (i.e., NucC) or components of toxin-antitoxin systems (i.e., AbiEii). To clarify the functional diversification of Cas10 proteins, we cloned, expressed, and purified five representatives from three phylogenetically distinct clades. None of the Cas10s are functional cyclases in isolation, and activity assays performed with polymerase domain active site mutants indicate that previously reported Cas10 DNA-polymerase activity may be a result of contamination. Collectively, this work helps clarify the phylogenetic and functional diversity of Cas10 proteins in type III CRISPR systems.

摘要

Cas10 蛋白是 III 型 CRISPR RNA(crRNA)引导的监测复合物的大亚基,其中许多具有核酸酶和环化酶活性。在这里,我们使用计算和系统发育方法从基因组和宏基因组数据库中鉴定和分析了 2014 个 Cas10 序列。Cas10 蛋白聚类为五个不同的分支,与先前建立的 CRISPR-Cas 亚型相对应。大多数 Cas10 蛋白(85.0%)具有保守的聚合酶活性位点基序,而 HD-核酸酶结构域的保守性较差(36.0%)。我们鉴定了 Cas10 变体,这些变体分布在多个基因上,或者与由环核苷酸(即 NucC)激活的核酸酶或毒素-抗毒素系统的组成部分(即 AbiEii)发生基因融合。为了阐明 Cas10 蛋白的功能多样化,我们从三个系统发育上不同的分支中克隆、表达和纯化了五个代表。没有一个 Cas10 蛋白在单独存在时是功能性的环化酶,并且聚合酶结构域活性位点突变体的活性测定表明,先前报道的 Cas10 DNA 聚合酶活性可能是污染的结果。总的来说,这项工作有助于阐明 III 型 CRISPR 系统中 Cas10 蛋白的系统发育和功能多样性。

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