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苯基汞胁迫通过破坏生长素稳态诱导根尖肿胀。

Phenylmercury stress induces root tip swelling through auxin homeostasis disruption.

作者信息

Uraguchi Shimpei, Sato Masakazu, Hagai Chihiro, Hirakawa Momoko, Ogawa Kotomi, Odagiri Miyu, Sato Haruka, Ohmori Ayaka, Ohshiro Yuka, Nakamura Ryosuke, Takanezawa Yasukazu, Kiyono Masako

机构信息

Department of Public Health, School of Pharmacy, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo, 108-8641, Japan.

出版信息

Plant Mol Biol. 2024 Dec 18;115(1):8. doi: 10.1007/s11103-024-01538-6.

Abstract

We previously reported that in Arabidopsis, the phytochelatin-mediated metal-detoxification machinery is also essential for organomercurial phenylmercury (PheHg) tolerance. PheHg treatment causes severe root growth inhibition in cad1-3, an Arabidopsis phytochelatin-deficient mutant, frequently accompanied by abnormal root tip swelling. Here, we examine morphological and physiological characteristics of PheHg-induced abnormal root tip swelling in comparison to Hg(II) stress and demonstrate that auxin homeostasis disorder in the root is associated with the PheHg-induced root tip swelling. Both Hg(II) and PheHg treatments severely inhibited root growth in cad1-3 and simultaneously induced the disappearance of starch-containing plastid amyloplasts in columella cells. However, further confocal imaging of the root tip revealed distinct effects of Hg(II) and PheHg toxicity on root cell morphology. PheHg treatment suppressed most major genes involved in auxin homeostasis, whereas these expression levels were up-regulated after 24 h of Hg(II) treatment. PheHg-triggered suppression of auxin transporters PIN1, PIN2, and PIN3 as GFP-fusion proteins was observed in the root tip, accompanied by an auxin reporter DR5rev::GFP signal reduction. Supplementation of indole-3-acetic acid (IAA) drastically canceled the PheHg-induced root swelling, however, Hg(II) toxicity was not mitigated by IAA. The presented results show that the collapse of auxin homeostasis especially in root tips is a cause for the abnormal root tip swelling under PheHg stress conditions.

摘要

我们之前报道过,在拟南芥中,植物螯合肽介导的金属解毒机制对于有机汞苯基汞(PheHg)耐受性也至关重要。PheHg处理会导致拟南芥植物螯合肽缺陷型突变体cad1-3的根生长严重受抑制,且常伴有根尖肿胀异常。在此,我们比较了PheHg诱导的根尖肿胀与Hg(II)胁迫下的形态和生理特征,并证明根中生长素稳态失调与PheHg诱导的根尖肿胀有关。Hg(II)和PheHg处理均严重抑制了cad1-3的根生长,并同时导致根冠细胞中含淀粉质体淀粉体消失。然而,根尖的进一步共聚焦成像揭示了Hg(II)和PheHg毒性对根细胞形态的不同影响。PheHg处理抑制了大多数参与生长素稳态的主要基因,而这些基因的表达水平在Hg(II)处理24小时后上调。在根尖观察到PheHg引发的生长素转运蛋白PIN1、PIN2和PIN3作为绿色荧光蛋白融合蛋白的抑制,同时生长素报告基因DR5rev::GFP信号降低。吲哚-3-乙酸(IAA)的补充极大地消除了PheHg诱导的根肿胀,然而,IAA并不能减轻Hg(II)的毒性。研究结果表明,生长素稳态的破坏,尤其是根尖部位,是PheHg胁迫条件下根尖肿胀异常的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d976/11655593/fd9501b1c665/11103_2024_1538_Fig1_HTML.jpg

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