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使用钙荧光蛋白钙传感器对钙信号峰值进行分析表明,结瘤基因表达受钙信号峰值数量和细胞发育状态的调控。

Analysis of calcium spiking using a cameleon calcium sensor reveals that nodulation gene expression is regulated by calcium spike number and the developmental status of the cell.

作者信息

Miwa Hiroki, Sun Jongho, Oldroyd Giles E D, Downie J Allan

机构信息

Department of Molecular Microbiology, John Innes Centre, Colney Lane, Norwich NR4 7UH, UK.

出版信息

Plant J. 2006 Dec;48(6):883-94. doi: 10.1111/j.1365-313X.2006.02926.x.

Abstract

Rhizobium-made Nod factors induce rapid changes in both Ca(2+) and gene expression. Mutations and inhibitors that abolish Nod-factor-induced Ca(2+) spiking block gene induction, indicating a specific role for Ca(2+) spiking in signal transduction. We used transgenic Medicago truncatula expressing a "cameleon" Ca(2+) sensor to assess the relationship between Nod-factor-induced Ca(2+) spiking and the activation of downstream gene expression. In contrast to ENOD11 induction, Ca(2+) spiking is activated in all root-hair cells and in epidermal or pre-emergent root hairs cells in the root tip region. Furthermore, cortical cells immediately below the epidermal layer also show slow Ca(2+) spiking and these cells lack Nod-factor-induced ENOD11 expression. This indicates a specialization in nodulation gene induction downstream of Nod-factor perception and signal transduction. There was a gradient in the frequency of Ca(2+) spiking along the root, with younger root-hair cells having a longer period between spikes than older root hairs. Using a Ca(2+)-pump inhibitor to block Ca(2+) spiking at various times after addition of Nod factor, we conclude that about 36 consecutive Ca(2+) spikes are sufficient to induce ENOD11-GUS expression in root hairs. To determine if the length of time of Ca(2+) spiking or the number of Ca(2+) spikes is more critical for Nod-factor-induced ENOD11 expression, jasmonic acid (JA) was added to reduce the rate of Nod-factor-induced Ca(2+) spiking. This revealed that even when the period between Ca(2+) spikes was extended, an equivalent number of Ca(2+) spikes were required for the induction of ENOD11. However, this JA treatment did not affect the spatial patterning of ENOD11-GUS expression suggesting that although a minimal number of Ca(2+) spikes are required for Nod-factor-induced gene expression, other factors restrict the expression of ENOD11 to a subset of responding cells.

摘要

根瘤菌产生的结瘤因子可迅速改变钙离子浓度和基因表达。消除结瘤因子诱导的钙离子峰的突变和抑制剂会阻断基因诱导,这表明钙离子峰在信号转导中具有特定作用。我们使用表达“cameleon”钙离子传感器的转基因蒺藜苜蓿来评估结瘤因子诱导的钙离子峰与下游基因表达激活之间的关系。与ENOD11诱导不同,钙离子峰在所有根毛细胞以及根尖区域的表皮或未伸出的根毛细胞中被激活。此外,紧挨着表皮层下方的皮层细胞也显示出缓慢的钙离子峰,并且这些细胞缺乏结瘤因子诱导的ENOD11表达。这表明在结瘤因子感知和信号转导下游的结瘤基因诱导存在特异性。沿着根,钙离子峰的频率存在梯度,较年轻的根毛细胞的峰间间隔比较老的根毛更长。在添加结瘤因子后的不同时间使用钙离子泵抑制剂来阻断钙离子峰,我们得出结论,大约36个连续的钙离子峰足以诱导根毛中ENOD11 - GUS的表达。为了确定钙离子峰的持续时间或钙离子峰的数量对于结瘤因子诱导的ENOD11表达哪个更关键,添加茉莉酸(JA)以降低结瘤因子诱导的钙离子峰的速率。这表明即使钙离子峰之间的间隔延长,诱导ENOD11仍需要等量的钙离子峰。然而,这种JA处理并不影响ENOD11 - GUS表达的空间模式,这表明尽管结瘤因子诱导的基因表达需要最少数量的钙离子峰,但其他因素将ENOD11的表达限制在一部分响应细胞中。

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