Tidwell Alyssa K, Faust Evelyn, Eckert Carrie A, Guss Adam M, Alexander William G
Biosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA.
The Bredesen Center for Interdisciplinary Research and Graduate Education, University of Tennessee-Knoxville, Knoxville, TN, USA.
J Ind Microbiol Biotechnol. 2024 Dec 31;52. doi: 10.1093/jimb/kuaf022.
Bacterial DNA methylation is involved in diverse cellular functions, including modulation of gene expression, DNA repair, and restriction-modification systems for defense against viruses and other foreign DNA. Restriction systems hinder efforts to engineer organisms to produce fuels and chemicals from waste and renewable feedstocks by degrading DNA during transformation. Methylome analysis allows identification of motifs within a bacterial chromosome that may be targeted by native restriction enzymes. Further expression of the corresponding methyltransferases in Escherichia coli allows plasmid DNA to be protected from restriction in the target organism, thereby drastically enhancing transformation efficiency. Nanopore sequencing can detect methylated bases, but software is needed to transform modified base coordinates into methylated motifs. Here, we develop MIJAMP (MIJAMP Is Just A MethylBED Parser), a software package that was developed to discover methylated motifs from the output of ONT's Modkit or other data in the methylBED format. MIJAMP employs a human-driven refinement strategy that empirically validates all motifs against genome-wide methylation data, thus eliminating incorrect motifs. MIJAMP also reports methylation data on specific, user-defined motifs. Using MIJAMP, we determined the methylated motifs both in a control strain (wild-type E. coli) and in Synecococcus sp. strain PCC7002, laying the foundation for improved transformation in this organism. MIJAMP is available at https://code.ornl.gov/alexander-public/mijamp/. One Sentence Summary: Here we describe software written to discover DNA methylation motifs from nanopore sequencing data.
细菌DNA甲基化参与多种细胞功能,包括基因表达调控、DNA修复以及用于抵御病毒和其他外来DNA的限制修饰系统。限制系统会在转化过程中降解DNA,从而阻碍利用工程生物体从废物和可再生原料生产燃料和化学品的努力。甲基化组分析能够识别细菌染色体中可能被天然限制酶靶向的基序。在大肠杆菌中进一步表达相应的甲基转移酶可使质粒DNA在目标生物体中免受限制,从而大幅提高转化效率。纳米孔测序能够检测甲基化碱基,但需要软件将修饰碱基坐标转化为甲基化基序。在此,我们开发了MIJAMP(MIJAMP只是一个甲基化BED解析器),这是一个软件包,旨在从ONT的Modkit输出或甲基化BED格式的其他数据中发现甲基化基序。MIJAMP采用人工驱动的优化策略,根据全基因组甲基化数据对所有基序进行实证验证,从而消除错误基序。MIJAMP还会报告特定的、用户定义基序的甲基化数据。利用MIJAMP,我们确定了对照菌株(野生型大肠杆菌)和聚球藻属菌株PCC7002中的甲基化基序,为改进该生物体的转化奠定了基础。MIJAMP可在https://code.ornl.gov/alexander - public/mijamp/获取。一句话总结:我们在此描述了用于从纳米孔测序数据中发现DNA甲基化基序的软件。