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首页> 外文期刊>Nucleic Acids Research >DNA motifs determining the accuracy of repeat duplication during CRISPR adaptation in Haloarcula hispanica
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DNA motifs determining the accuracy of repeat duplication during CRISPR adaptation in Haloarcula hispanica

机译:DNA基序决定了在Halolarcula hispanica中CRISPR适应过程中重复重复的准确性

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摘要

Clustered Regularly Interspaced Short Palindromic Repeats (CRISPRs) acquire new spacers to generate adaptive immunity in prokaryotes. During spacer integration, the leader-preceded repeat is always accurately duplicated, leading to speculations of a repeat-length ruler. Here in Haloarcula hispanica, we demonstrate that the accurate duplication of its 30-bp repeat requires two conserved mid-repeat motifs, AACCC and GTGGG. The AACCC motif was essential and needed to be similar to 10 bp downstream from the leader-repeat junction site, where duplication consistently started. Interestingly, repeat duplication terminated sequence-independently and usually with a specific distance from the GTGGG motif, which seemingly served as an anchor site for a molecular ruler. Accordingly, altering the spacing between the two motifs led to an aberrant duplication size (29, 31, 32 or 33 bp). We propose the adaptation complex may recognize these mid-repeat elements to enable measuring the repeat DNA for spacer integration.
机译:簇状规则间隔的短回文重复序列(CRISPR)获得了新的间隔子,以在原核生物中产生适应性免疫。在间隔器整合过程中,始终会精确复制前导序列之前的重复序列,从而推测出重复序列长度标尺。在这里,我们展示了其在Halolarcula hispanica中的30 bp重复的准确重复,需要两个保守的中间重复基序AACCC和GTGGG。 AACCC主题是必不可少的,需要与前导重复序列连接位点下游的10 bp相似,在那里重复不断地开始复制。有趣的是,重复复制独立于序列终止,通常距GTGGG基序有特定距离,后者似乎充当了分子标尺的锚定位点。因此,改变两个基序之间的间隔导致异常的重复大小(29、31、32或33bp)。我们提出,适应复合物可以识别这些中间重复元件,从而能够测量重复DNA进行间隔子整合。

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