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Genetic determinants of PAM-dependent DNA targeting and pre-crRNA processing in Sulfolobus islandicus

机译:岛S对PAM依赖的DNA靶向和crRNA前加工的遗传决定因素。

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Bacteria and Archaea encode clustered, regularly interspaced, short palindromic repeat (CRISPR) systems to confer adaptive immunity to invasive viruses and plasmids. Recent studies of CRISPR systems revealed that diverse CRISPR-associated (Cas) interference modules often coexist in different organisms but functions of cas genes have not been dissected in any of these systems. The crenarchaeon Sulfolobus islandicus encodes three distinct CRISPR interference modules, including a type IA system and two type IIIB systems: Cmr-α and Cmr-β. To study the genetic determinants of protospacer-adjacent motif (PAM)-dependent DNA targeting activity and mature CRISPR RNA (crRNA) production in this organism, mutants deleting individual genes of the type IA system or removing each of other Cas modules were constructed. Characterization of these mutants revealed that Cas7, Cas5, Cas6, Cas3′ and Cas3″ are essential for PAM-dependent DNA targeting activity, whereas Csa5, along with all other Cas modules, is dispensable for the targeting in the crenarchaeon. Cas6 is implicated as the only enzyme for pre-crRNA processing and the crRNA maturation is independent of the DNA targeting activity. Importantly, we show that Cas7 and Cas5 are essential for stabilizing the processing intermediates and mature crRNAs, respectively, and that depleting the helicase or nuclease domain of Cas3 leads to the accumulation of processing intermediates. This demonstrates that in addition to Cas6, other Cas proteins of an archaeal type IA system also contribute to crRNA processing.
机译:细菌和古细菌编码成簇的,规则间隔的短回文重复(CRISPR)系统,以赋予对侵入性病毒和质粒的适应性免疫力。 CRISPR系统的最新研究表明,多种CRISPR相关(Cas)干扰模块通常共存于不同生物中,但是cas基因的功能尚未在任何这些系统中进行剖析。 Crnarchaeon Sulfolobus islandicus编码三个不同的CRISPR干扰模块,包括IA型系统和两个IIIB型系统:Cmr-α和Cmr-β。为了研究这种生物中前间隔物相邻基序(PAM)依赖性DNA靶向活性和成熟CRISPR RNA(crRNA)产生的遗传决定因素,构建了删除IA型系统单个基因或删除其他Cas模块的突变体。这些突变体的表征表明,Cas7,Cas5,Cas6,Cas3'和Cas3''对于依赖PAM的DNA靶向活性必不可少,而Csa5以及所有其他Cas模块对于在鱼骨中靶向是必不可少的。 Cas6被认为是crrRNA加工前的唯一酶,而crRNA的成熟与DNA靶向活性无关。重要的是,我们显示Cas7和Cas5分别对稳定加工中间体和成熟crRNA至关重要,并且耗尽Cas3的解旋酶或核酸酶结构域会导致加工中间体的积累。这表明除了Cas6之外,古细菌IA型系统的其他Cas蛋白也有助于crRNA加工。

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