category
NAR
date
Feb 23, 2026
slug
status
Published
summary
首次系统解析3000余种细菌DNA聚合酶的丰度分布规律,发现Y家族最丰富且存在11种新型多聚错误易错复合物,揭示了不同细菌谱系、复制系统类型和环境因素对聚合酶分布模式的塑造作用。
tags
蛋白质组学
蛋白质进化
核酸蛋白工具酶
type
Post

📄 原文题目

Diversity and distribution of bacterial DNA polymerases

🔗 原文链接

💡 AI 核心解读

首次系统解析3000余种细菌DNA聚合酶的丰度分布规律,发现Y家族最丰富且存在11种新型多聚错误易错复合物,揭示了不同细菌谱系、复制系统类型和环境因素对聚合酶分布模式的塑造作用。

📝 英文原版摘要

<span class="paragraphSection"><div class="boxTitle">Abstract</div>DNA polymerases are key players in DNA replication, repair, and maintenance. However, the overall abundance, diversity, and distribution of bacterial DNA polymerases have not been systematically explored. To close this knowledge gap, we computationally identified and characterized DNA polymerases and their homologs from A, B, C, X, and Y families in over 3000 representative bacterial species with complete genomes. We found that Y-family is the most abundant, followed by C and A families, whereas B and X families are rare. All species have replicative C-family polymerases, 96% have A-family polymerases, and 88% have Y-family members. In each family, we identified and annotated distinct groups, proofreading nucleases, and interaction motifs. Based on conserved associations for DnaE2 and Y-family groups, we identified 11 types of putative multimeric error-prone DNA polymerases supported by AlphaFold modeling. Approximately 90% of the complexes belong to four major types, exemplified by <span style="font-style: italic;">Meiothermus silvanus</span> PolY–RecA complex, <span style="font-style: italic;">Mycobacterium tuberculosis</span> ImuA–ImuB–DnaE2, <span style="font-style: italic;">Escherichia coli</span> Pol V (UmuC–UmuD′<sub>2</sub>–RecA), and <span style="font-style: italic;">Bacillus subtilis</span> YqjW–YqjX–RecA. We found that distribution patterns of distinct polymerase groups and multimeric complexes are shaped by bacterial lineages, replication-system types, and environmental factors. Our results thus provide a comprehensive picture of DNA polymerase diversity and distribution across the bacterial domain.</span>
CFP1介导的H3K4me3广域结构控制早期B细胞谱系命运决定保守的古菌核糖体相关因子连接细菌休眠与真核生物能量感知
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