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电子显微镜揭示了大肠杆菌胸腺嘧啶缺乏死亡过程中出乎意料的细胞质和包膜变化。

Electron Microscopy Reveals Unexpected Cytoplasm and Envelope Changes during Thymineless Death in Escherichia coli.

机构信息

Department of Microbiology, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.

出版信息

J Bacteriol. 2021 Aug 9;203(17):e0015021. doi: 10.1128/JB.00150-21.

Abstract

Bacterial rod-shaped cells experiencing irreparable chromosome damage should filament without other morphological changes. Thymineless death (TLD) strikes thymidine auxotrophs denied external thymine/thymidine (T) supplementation. Such T-starved cells cannot produce the DNA precursor dTTP and therefore stop DNA replication. Stalled replication forks in T-starved cells were always assumed to experience mysterious chromosome lesions, but TLD was recently found to happen even without origin-dependent DNA replication, with the chromosome still remaining the main TLD target. T starvation also induces morphological changes, as if thymidine prevents cell envelope or cytoplasm problems that otherwise translate into chromosome damage. Here, we used transmission electron microscopy (TEM) to examine cytoplasm and envelope changes in T-starved Escherichia coli cells, using treatment with a DNA gyrase inhibitor as a control for "pure" chromosome death. Besides the expected cell filamentation in response to both treatments, we see the following morphological changes specific for T starvation and which might lead to chromosome damage: (i) significant cell widening, (ii) nucleoid diffusion, (iii) cell pole damage, and (iv) formation of numerous cytoplasmic bubbles. We conclude that T starvation does impact both the cytoplasm and the cell envelope in ways that could potentially affect the chromosome. Thymineless death is a dramatic and medically important phenomenon, the mechanisms of which remain a mystery. Unlike most other auxotrophs in the absence of the required supplement, thymidine-requiring E. coli mutants not only go static in the absence of thymidine, but rapidly die of chromosomal damage of unclear nature. Since this chromosomal damage is independent of replication, we examined fine morphological changes in cells undergoing thymineless death in order to identify what could potentially affect the chromosome. Here, we report several cytoplasm and cell envelope changes that develop in thymidine-starved cells but not in gyrase inhibitor-treated cells (negative control) that could be linked to subsequent irreparable chromosome damage. This is the first electron microscopy study of cells undergoing "genetic death" due to irreparable chromosome lesions.

摘要

经历不可修复染色体损伤的细菌杆状细胞应该在没有其他形态变化的情况下发生丝状化。胸腺嘧啶饥饿死亡(TLD)会影响缺乏外部胸腺嘧啶/胸苷(T)补充的胸腺嘧啶营养缺陷型。这种 T 饥饿的细胞无法产生 DNA 前体 dTTP,因此停止 DNA 复制。在 T 饥饿的细胞中,停滞的复制叉总是被认为会经历神秘的染色体损伤,但最近发现,即使没有依赖于原点的 DNA 复制,TLD 也会发生,而染色体仍然是 TLD 的主要靶点。T 饥饿还会诱导形态变化,就好像胸苷可以防止细胞包膜或细胞质问题转化为染色体损伤一样。在这里,我们使用透射电子显微镜(TEM)检查 T 饥饿的大肠杆菌细胞的细胞质和包膜变化,使用 DNA 拓扑异构酶抑制剂处理作为“纯”染色体死亡的对照。除了对两种处理都预期的细胞丝状化外,我们还观察到以下特定于 T 饥饿的形态变化,这可能导致染色体损伤:(i)细胞显著变宽,(ii)核体扩散,(iii)细胞极损伤,和(iv)形成许多细胞质泡。我们得出结论,T 饥饿确实会影响细胞质和细胞包膜,从而可能影响染色体。胸腺嘧啶饥饿死亡是一种戏剧性且具有重要医学意义的现象,其机制仍然是一个谜。与缺乏所需补充物的大多数其他营养缺陷型不同,需要胸苷的大肠杆菌突变体不仅在缺乏胸苷的情况下会静止,而且会迅速因不明性质的染色体损伤而死亡。由于这种染色体损伤独立于复制,我们检查了经历胸腺嘧啶饥饿死亡的细胞中的精细形态变化,以确定哪些可能会影响染色体。在这里,我们报告了在胸苷饥饿的细胞中发生但在拓扑异构酶抑制剂处理的细胞(阴性对照)中未发生的几种细胞质和细胞包膜变化,这些变化可能与随后不可修复的染色体损伤有关。这是首次用电镜研究由于不可修复的染色体损伤而导致的“遗传死亡”细胞。

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本文引用的文献

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Thymineless Death Lives On: New Insights into a Classic Phenomenon.胸腺嘧啶缺乏性死亡仍在继续:对经典现象的新认识。
Annu Rev Microbiol. 2015;69:247-63. doi: 10.1146/annurev-micro-092412-155749. Epub 2015 Aug 7.

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