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Systematic analysis of Type I-E Escherichia coli CRISPR-Cas PAM sequences ability to promote interference and primed adaptation

机译:I-E型大肠杆菌CAM CAM序列促进干扰和灌注调整的系统分析

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CRISPR interference occurs when a protospacer recognized by the CRISPR RNA is destroyed by Cas effectors. In Type I CRISPR-Cas systems, protospacer recognition can lead to > - acquisition of new spacers from in cis located sequences. Type I CRISPR-Cas systems require the presence of a trinucleotide protospacer adjacent motif (PAM) for efficient interference. Here, we investigated the ability of each of 64 possible trinucleotides located at the PAM position to induce CRISPR interference and primed adaptation by the Escherichia coli Type I-E CRISPR-Cas system. We observed clear separation of PAM variants into three groups: those unable to cause interference, those that support rapid interference and those that lead to reduced interference that occurs over extended periods of time. PAM variants unable to support interference also did not support primed adaptation; those that supported rapid interference led to no or low levels of adaptation, while those that caused attenuated levels of interference consistently led to highest levels of adaptation. The results suggest that primed adaptation is fueled by the products of CRISPR interference. Extended over time interference with targets containing > PAM variants provides a continuous source of new spacers leading to high overall level of spacer acquisition.
机译:当CRISPR RNA识别的原始扫描器被CAS效应器销毁时,发生CRISPR干扰。在I型CRISPR-CAS系统中,ProTospacer识别可以导致> - 从CIS定位序列中获取新的垫片。 I型CRISPR-CAS系统需要存在突蛋白激素相邻的基序(PAM)以获得有效干扰。在这里,我们研究了位于PAM位置的64种可能的三核苷酸中的每一个的能力,以诱导CIScherichia Coli型I-E CRISPR-CAS系统诱导Crisp的干扰和灌注调整。我们观察到PAM变体的清晰分离为三组:无法引起干扰的那些,那些支持快速干扰的人和导致在延长的时间段发生的干扰减少干扰。 PAM Variants无法支持干扰也不支持Primed Adaption;支持快速干扰的人导致了无或低水平的适应水平,而导致减弱的干扰水平的那些始终如一地导致最高水平的适应。结果表明,CRISPR干扰的产品促进了引发的适应。随着时间的推移,与包含> PAM变体的目标的干扰提供了一个连续的新垫片来源,导致高层间隔级采集。

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