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The role of Arabidopsis aldehyde dehydrogenase genes in response to high temperature and stress combinations.拟南芥醛脱氢酶基因在应对高温和胁迫组合中的作用。
J Exp Bot. 2017 Jul 10;68(15):4295-4308. doi: 10.1093/jxb/erx194.
2
Extra Large G-Protein Interactome Reveals Multiple Stress Response Function and Partner-Dependent XLG Subcellular Localization.超大G蛋白相互作用组揭示多种应激反应功能及依赖伴侣的XLG亚细胞定位。
Front Plant Sci. 2017 Jun 13;8:1015. doi: 10.3389/fpls.2017.01015. eCollection 2017.
3
Membranes as Structural Antioxidants: RECYCLING OF MALONDIALDEHYDE TO ITS SOURCE IN OXIDATION-SENSITIVE CHLOROPLAST FATTY ACIDS.作为结构抗氧化剂的膜:丙二醛在对氧化敏感的叶绿体脂肪酸中的来源循环利用。
J Biol Chem. 2016 Jun 17;291(25):13005-13. doi: 10.1074/jbc.M116.729921. Epub 2016 May 3.
4
Overexpression of ALDH10A8 and ALDH10A9 Genes Provides Insight into Their Role in Glycine Betaine Synthesis and Affects Primary Metabolism in Arabidopsis thaliana.ALDH10A8和ALDH10A9基因的过表达有助于深入了解它们在甘氨酸甜菜碱合成中的作用,并影响拟南芥的初级代谢。
Plant Cell Physiol. 2015 Sep;56(9):1798-807. doi: 10.1093/pcp/pcv105. Epub 2015 Jul 13.
5
Lipid Peroxide-Derived Short-Chain Carbonyls Mediate Hydrogen Peroxide-Induced and Salt-Induced Programmed Cell Death in Plants.脂质过氧化物衍生的短链羰基化合物介导植物中过氧化氢诱导和盐诱导的程序性细胞死亡。
Plant Physiol. 2015 Jul;168(3):885-98. doi: 10.1104/pp.115.256834. Epub 2015 May 29.
6
Cytoplastic Glyceraldehyde-3-Phosphate Dehydrogenases Interact with ATG3 to Negatively Regulate Autophagy and Immunity in Nicotiana benthamiana.细胞质甘油醛-3-磷酸脱氢酶与ATG3相互作用以负向调节本氏烟草中的自噬和免疫。
Plant Cell. 2015 Apr;27(4):1316-31. doi: 10.1105/tpc.114.134692. Epub 2015 Mar 31.
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Arabidopsis glutaredoxin S17 and its partner, the nuclear factor Y subunit C11/negative cofactor 2α, contribute to maintenance of the shoot apical meristem under long-day photoperiod.拟南芥谷氧还蛋白S17及其伙伴核因子Y亚基C11/负辅因子2α,有助于在长日照光周期下维持茎尖分生组织。
Plant Physiol. 2015 Apr;167(4):1643-58. doi: 10.1104/pp.15.00049. Epub 2015 Feb 19.
8
Identification of oxidatively modified proteins in salt-stressed Arabidopsis: a carbonyl-targeted proteomics approach.盐胁迫下拟南芥中氧化修饰蛋白质的鉴定:一种针对羰基的蛋白质组学方法。
Plant Cell Physiol. 2014 Jul;55(7):1233-44. doi: 10.1093/pcp/pcu072. Epub 2014 May 21.
9
Sequence and functional analyses of the aldehyde dehydrogenase 7B4 gene promoter in Arabidopsis thaliana and selected Brassicaceae: regulation patterns in response to wounding and osmotic stress.拟南芥和选定十字花科植物中醛脱氢酶7B4基因启动子的序列和功能分析:对伤口和渗透胁迫的响应调控模式
Planta. 2014 Jun;239(6):1281-98. doi: 10.1007/s00425-014-2051-0. Epub 2014 Mar 12.
10
Interaction of aldehydes derived from lipid peroxidation and membrane proteins.脂质过氧化衍生的醛类与膜蛋白的相互作用。
Front Physiol. 2013 Sep 4;4:242. doi: 10.3389/fphys.2013.00242.

醛脱氢酶可能通过脂质过氧化衍生的生物活性醛来调节信号传导。

Aldehyde dehydrogenases may modulate signaling by lipid peroxidation-derived bioactive aldehydes.

作者信息

Tagnon Missihoun D, Simeon Kotchoni O

机构信息

a Department of Biology , Rutgers University , Camden , NJ , USA.

b Center for Computational and Integrative Biology , Rutgers University , Camden , NJ , USA.

出版信息

Plant Signal Behav. 2017 Nov 2;12(11):e1387707. doi: 10.1080/15592324.2017.1387707. Epub 2017 Oct 9.

DOI:10.1080/15592324.2017.1387707
PMID:28990846
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5703241/
Abstract

Aldehyde molecules were shown to induce gene expression but because of their toxicity, the cell expresses ALDEHYDE DEHYDROGENASES (ALDH, EC 1.2.1.3) that oxidize them to carboxylic acids. To understand how the aldehydes may be both toxic and gene activators, we expressed the ALDH7B4 gene promoter fused to the β-glucuronidase reporter gene in independent transgenic lines and found that pentanal and trans-2-hexenal activated the promoter whereas trans-2-hexenal induced the ALDH7B4 protein. Paraquat led to higher amounts of malondialdehyde compared to trans-2-hexenal and HO, and only the treatment by Paraquat activated the ALDH7B4 promoter, indicating that a threshold level of aldehydes is required for gene activation. These findings suggest that ALDH activity may also serve to fine-tune gene activation by the aldehydes.

摘要

醛分子被证明可诱导基因表达,但由于其毒性,细胞会表达醛脱氢酶(ALDH,EC 1.2.1.3),将醛氧化为羧酸。为了解醛如何既具有毒性又能激活基因,我们在独立的转基因系中表达了与β-葡萄糖醛酸酶报告基因融合的ALDH7B4基因启动子,发现戊醛和反式-2-己烯醛可激活该启动子,而反式-2-己烯醛可诱导ALDH7B4蛋白。与反式-2-己烯醛和过氧化氢相比,百草枯导致更高含量的丙二醛,并且只有百草枯处理可激活ALDH7B4启动子,这表明基因激活需要醛达到阈值水平。这些发现表明,ALDH活性也可能用于微调醛对基因的激活作用。