高密度 CRISPRi 筛选揭示了改善蓝藻适应性的多种途径

IF 9.1 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Andrew Hren, Nicole Lollini, Dana L. Carper, Paul E. Abraham, Jeffrey C. Cameron, Jerome M. Fox, Carrie A. Eckert
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引用次数: 0

摘要

蓝藻是地球上最古老的光合生命形式,从永久冻土到温泉,几乎所有栖息地都有蓝藻的初级生产。尽管长期以来人们对这些微生物的驯化很感兴趣,但对它们的理解仍然很差,重新布线也很有挑战性。本研究采用高密度全基因组CRISPR干扰筛选,检测极端环境下基因特异性转录变异对聚球菌PCC 7002生长的影响。令人惊讶的是,许多部分敲除增强了在寒冷单色条件下的适应性。NDH-1复合体核心亚基基因的转录抑制对光合作用和碳吸收很重要,在红光和蓝光下都提高了生长速度,但在不同的颜色特异性最佳状态下。大多数具有改善适应度敲低的基因对每种浅色都是不同的,双靶点转录抑制产生非加性效应。研究结果揭示了蓝细菌改善适应的多种途径(例如,参与CO 2吸收、光收集、翻译和嘌呤代谢的基因的衰减),并提供了一种利用sgRNA活性梯度来确定细胞中生化影响的转录变化的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High-density CRISPRi screens reveal diverse routes to improved acclimation in cyanobacteria
Cyanobacteria are the oldest form of photosynthetic life on Earth and contribute to primary production in nearly every habitat, from permafrost to hot springs. Despite longstanding interest in the acclimation of these microbes, it remains poorly understood and challenging to rewire. This study uses a high-density, genome-wide CRISPR interference screen to examine the influence of gene-specific transcriptional variation on the growth of Synechococcus sp. PCC 7002 under environmental extremes. Surprisingly, many partial knockdowns enhanced fitness under cold monochromatic conditions. Transcriptional repression of genes for core subunits of the NDH-1 complex, which are important for photosynthesis and carbon uptake, improved growth rates under both red and blue light but at distinct, color-specific optima. Most genes with fitness-improving knockdowns were distinct to each light color, and dual-target transcriptional repression produced nonadditive effects. Findings reveal diverse routes to improved acclimation in cyanobacteria (e.g., attenuation of genes involved in CO 2 uptake, light harvesting, translation, and purine metabolism) and provide an approach for using gradients in sgRNA activity to pinpoint biochemically influential transcriptional changes in cells.
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来源期刊
CiteScore
19.00
自引率
0.90%
发文量
3575
审稿时长
2.5 months
期刊介绍: The Proceedings of the National Academy of Sciences (PNAS), a peer-reviewed journal of the National Academy of Sciences (NAS), serves as an authoritative source for high-impact, original research across the biological, physical, and social sciences. With a global scope, the journal welcomes submissions from researchers worldwide, making it an inclusive platform for advancing scientific knowledge.
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