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通过解决同一菌株的两个完整基因组之间的差异,并揭示粘球菌门中Mx-α原噬菌体区域的多样性,创建DZ2的一致性基因组组装。

Creating a consensus genome assembly of DZ2 by resolving discrepancies between two complete genomes of the same strain and uncovering the Mx-alpha prophage region diversity across phylum Myxococcota.

作者信息

Mahanta Utkarsha, Sharma Gaurav

机构信息

Department of Biotechnology, Indian Institute of Technology Hyderabad, Sangareddy, Telangana, India.

出版信息

NAR Genom Bioinform. 2025 Aug 27;7(3):lqaf112. doi: 10.1093/nargab/lqaf112. eCollection 2025 Sep.

Abstract

DZ2, a model myxobacterium, has three reported genome assemblies, including two recent complete assemblies (MxDZ2_Tam and MxDZ2_Nan) from the same culture stock. These assemblies misreported their circular nature and differed by 6.4 kb, raising questions about their accuracy. After removing duplicate ends, aligning genomes to the origin of replication, and circularization, this computational analysis revealed a minimal 32 bp difference, with MxDZ2_Tam being slightly larger. Forty sequence variations including 38 indels and two substitutions, were impacting 18 coding genes via frameshift mutations. Although PacBio-HiFi technology boasts a low error rate, it remains higher than the 454-platform used for the earlier MxDZ2_Kirby draft assembly. Therefore, using MxDZ2_Kirby as a reference, we constructed a "truly circular" genome for DZ2. Additionally, analysis of Mx-alpha regions, involved in antagonism via the toxin gene , across 61 myxobacterial genomes identified their presence in five taxonomically polyphyletic species, potentially influencing their physiology, development, and ecological interactions beyond predation. Only DZ2 and DZF1 contained all three Mx-alpha regions, whereas DK1622 has only one. Overall, this study underscores the need for meticulous validation of sequencing-based genome assemblies and their variations and provides novel insights into Mx-alpha regions as potential adaptive elements in myxobacteria.

摘要

模式黏细菌DZ2有三个已报道的基因组组装结果,包括来自同一培养株系的两个近期完整组装结果(MxDZ2_Tam和MxDZ2_Nan)。这些组装结果错误地报告了它们的环状性质,且相差6.4 kb,这引发了对其准确性的质疑。在去除重复末端、将基因组与复制起点比对并环化后,这项计算分析揭示出最小差异为32 bp,其中MxDZ2_Tam略大。40个序列变异,包括38个插入缺失和两个替换,通过移码突变影响了18个编码基因。尽管PacBio-HiFi技术的错误率较低,但仍高于用于早期MxDZ2_Kirby草图组装的454平台。因此,以MxDZ2_Kirby为参考,我们构建了DZ2的“真正环状”基因组。此外,通过对61个黏细菌基因组中涉及通过毒素基因进行拮抗作用的Mx-α区域的分析,发现在五个分类学上多系的物种中存在这些区域,这可能会影响它们除捕食之外的生理、发育和生态相互作用。只有DZ2和DZF1包含所有三个Mx-α区域,而DK1622只有一个。总体而言,这项研究强调了对基于测序的基因组组装及其变异进行细致验证的必要性,并为Mx-α区域作为黏细菌潜在适应性元件提供了新见解。

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