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一种泛基因组方法来确定 和 基因组的核心区域。

A pan-genome method to determine core regions of the and genomes.

机构信息

J. Craig Venter Institute, Rockville, Maryland, 20850, USA.

Natural Selection, Inc., San Diego, CA, 92121, USA.

出版信息

F1000Res. 2021 Apr 13;10:286. doi: 10.12688/f1000research.51873.2. eCollection 2021.

Abstract

Synthetic engineering of bacteria to produce industrial products is a burgeoning field of research and application. In order to optimize genome design, designers need to understand which genes are essential, which are optimal for growth, and locations in the genome that will be tolerated by the organism when inserting engineered cassettes. We present a pan-genome based method for the identification of core regions in a genome that are strongly conserved at the species level. We show that the core regions determined by our method contain all or almost all essential genes. This demonstrates the accuracy of our method as essential genes should be core genes. We show that we outperform previous methods by this measure. We also explain why there are exceptions to this rule for our method. We assert that synthetic engineers should avoid deleting or inserting into these core regions unless they understand and are manipulating the function of the genes in that region. Similarly, if the designer wishes to streamline the genome, non-core regions and in particular low penetrance genes would be good targets for deletion. Care should be taken to remove entire cassettes with similar penetrance of the genes within cassettes as they may harbor toxin/antitoxin genes which need to be removed in tandem. The bioinformatic approach introduced here saves considerable time and effort relative to knockout studies on single isolates of a given species and captures a broad understanding of the conservation of genes that are core to a species.

摘要

细菌的合成工程是一个新兴的研究和应用领域。为了优化基因组设计,设计师需要了解哪些基因是必需的,哪些基因最适合生长,以及在向生物体中插入工程化盒时基因组中哪些位置是可以容忍的。我们提出了一种基于泛基因组的方法,用于识别基因组中在物种水平上强烈保守的核心区域。我们表明,我们的方法确定的核心区域包含所有或几乎所有必需基因。这证明了我们方法的准确性,因为必需基因应该是核心基因。我们通过这一指标表明我们优于以前的方法。我们还解释了为什么我们的方法存在例外。我们断言,合成工程师应该避免删除或插入这些核心区域,除非他们了解并正在操作该区域中的基因的功能。同样,如果设计师希望简化基因组,非核心区域,特别是低渗透率基因将是删除的良好目标。应该小心地去除具有相似渗透率的整个盒中的基因,因为它们可能含有需要串联去除的毒素/抗毒素基因。这里介绍的生物信息学方法相对于对给定物种的单个分离株进行敲除研究节省了大量的时间和精力,并广泛了解了对物种核心至关重要的基因的保守性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae8b/8420889/361e541a8bd0/f1000research-10-76417-g0000.jpg

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