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质体基因组不稳定性导致拟南芥中活性氧的产生和质体到细胞核的逆行信号转导。

Plastid genome instability leads to reactive oxygen species production and plastid-to-nucleus retrograde signaling in Arabidopsis.

机构信息

Department of Biochemistry, Université de Montréal, Montreal, Quebec, Canada H3C 3J7.

出版信息

Plant Physiol. 2013 Oct;163(2):867-81. doi: 10.1104/pp.113.223560. Epub 2013 Aug 22.

Abstract

The plastid genome is highly conserved among plant species, suggesting that alterations of its structure would have dramatic impacts on plant fitness. Nevertheless, little is known about the direct consequences of plastid genome instability. Recently, it was reported that the plastid Whirly proteins WHY1 and WHY3 and a specialized type-I polymerase, POLIB, act as safeguards against plastid genome instability in Arabidopsis (Arabidopsis thaliana). In this study, we use ciprofloxacin, an organelle double-strand break-inducing agent, and the why1why3polIb-1 variegated mutant to evaluate the impact of generalized plastid DNA instability. First, we show that in why1why3polIb-1 and ciprofloxacin-treated plants, plastid genome instability is associated with increased reactive oxygen species production. Then, using different light regimens, we show that the elevated reactive oxygen species production correlates with the appearance of a yellow-variegated phenotype in the why1why3polIb-1 population. This redox imbalance also correlates to modifications of nuclear gene expression patterns, which in turn leads to acclimation to high light. Taken together, these results indicate that plastid genome instability induces an oxidative burst that favors, through nuclear genetic reprogramming, adaptation to subsequent oxidative stresses.

摘要

质体基因组在植物物种中高度保守,这表明其结构的改变将对植物的适应性产生巨大影响。然而,关于质体基因组不稳定性的直接后果知之甚少。最近,有报道称质体 Whirly 蛋白 WHY1 和 WHY3 以及一种特殊类型的 I 型聚合酶 POLIB,在拟南芥(Arabidopsis thaliana)中作为质体基因组不稳定性的保护因子。在这项研究中,我们使用环丙沙星(一种诱导细胞器双链断裂的试剂)和 why1why3polIb-1 斑驳突变体来评估广义质体 DNA 不稳定性的影响。首先,我们表明在 why1why3polIb-1 和环丙沙星处理的植物中,质体基因组不稳定性与活性氧物质产生的增加有关。然后,我们使用不同的光照方案表明,活性氧物质的产生与 why1why3polIb-1 群体中出现黄色斑驳表型有关。这种氧化还原失衡也与核基因表达模式的改变有关,这反过来又导致了对高光的适应。总之,这些结果表明,质体基因组不稳定性诱导了氧化爆发,通过核遗传重编程,有利于适应随后的氧化应激。

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