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细菌和古菌中的毒素-抗毒素系统。

Toxin-antitoxin systems in bacteria and archaea.

机构信息

Department of Biochemistry, Center for Advanced Biotechnology and Medicine, Robert Wood Johnson Medical School, Piscataway, New Jersey 08854, USA.

出版信息

Annu Rev Genet. 2011;45:61-79. doi: 10.1146/annurev-genet-110410-132412.

Abstract

Almost all bacteria and many archaea contain genes whose expression inhibits cell growth and may lead to cell death when overproduced, reminiscent of apoptotic genes in higher systems. The cellular targets of these toxins are quite diverse and include DNA replication, mRNA stability, protein synthesis, cell-wall biosynthesis, and ATP synthesis. These toxins are co-expressed and neutralized with their cognate antitoxins from a TA (toxin-antitoxin) operon in normally growing cells. Antitoxins are more labile than toxins and are readily degraded under stress conditions, allowing the toxins to exert their toxic effect. Presence of at least 33 TA systems in Escherichia coli and more than 60 TA systems in Mycobacterium tuberculosis suggests that the TA systems are involved not only in normal bacterial physiology but also in pathogenicity of bacteria. The elucidation of their cellular function and regulation is thus crucial for our understanding of bacterial physiology under various stress conditions.

摘要

几乎所有细菌和许多古菌都含有表达抑制细胞生长的基因,当这些基因过量表达时,可能会导致细胞死亡,这让人联想到高等生物系统中的凋亡基因。这些毒素的细胞靶标非常多样化,包括 DNA 复制、mRNA 稳定性、蛋白质合成、细胞壁生物合成和 ATP 合成。在正常生长的细胞中,这些毒素与其同源的抗毒素一起从 TA(毒素-抗毒素)操纵子中共同表达并中和。抗毒素比毒素更不稳定,在应激条件下容易降解,从而使毒素发挥其毒性作用。大肠杆菌中至少存在 33 个 TA 系统,结核分枝杆菌中存在 60 多个 TA 系统,这表明 TA 系统不仅参与细菌的正常生理过程,而且参与细菌的致病性。因此,阐明它们的细胞功能和调节机制对于我们理解各种应激条件下的细菌生理至关重要。

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