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I 型-E 大肠埃希菌 CRISPR-Cas PAM 序列促进干扰和引物适应能力的系统分析。

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

机构信息

Center of Life Sciences, Skolkovo Institute of Science and Technology, Moscow, 121205, Russia.

Institute of Molecular Genetics, Russian Academy of Sciences, Moscow, 123182, Russia.

出版信息

Mol Microbiol. 2019 Jun;111(6):1558-1570. doi: 10.1111/mmi.14237. Epub 2019 Apr 6.

Abstract

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 «primed adaptation» - 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 «attenuated» PAM variants provides a continuous source of new spacers leading to high overall level of spacer acquisition.

摘要

当被 CRISPR RNA 识别的原间隔序列被 Cas 效应子破坏时,就会发生 CRISPR 干扰。在 I 型 CRISPR-Cas 系统中,原间隔序列的识别可导致“引物适应”——从顺式定位的序列中获取新的间隔序列。I 型 CRISPR-Cas 系统需要三核苷酸原间隔序列相邻基序(PAM)的存在才能进行有效的干扰。在这里,我们研究了 64 种可能的三核苷酸在 PAM 位置的每个核苷酸,以诱导大肠杆菌 I 型-E CRISPR-Cas 系统的 CRISPR 干扰和引物适应。我们观察到 PAM 变体明显分为三组:那些不能引起干扰的、那些支持快速干扰的和那些导致干扰时间延长的。不能支持干扰的 PAM 变体也不支持引物适应;那些支持快速干扰的不会导致适应,而那些导致干扰减弱的则会导致最高水平的适应。结果表明,引物适应是由 CRISPR 干扰的产物驱动的。随着时间的推移,对含有“衰减”PAM 变体的靶标的干扰提供了一个新的间隔序列的连续来源,从而导致总体水平的间隔序列获取较高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad5c/6865019/a8e18f1dd9f5/MMI-111-1558-g001.jpg

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