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过氧化氢酶、谷胱甘肽和蛋白磷酸酶 2A 依赖性细胞器氧化还原信号调节中强光照下和高光强下蚜虫的繁殖力。

Catalase, glutathione, and protein phosphatase 2A-dependent organellar redox signalling regulate aphid fecundity under moderate and high irradiance.

机构信息

School of Biosciences, College of Life and Environmental Sciences, University of Birmingham, Edgbaston, B15 2TT, UK.

Technical College of Applied Science, Sulaimani Polytechnic University, 46001, Sulaymaniyah, Iraq.

出版信息

Plant Cell Environ. 2020 Jan;43(1):209-222. doi: 10.1111/pce.13669. Epub 2019 Nov 14.

Abstract

Redox processes regulate plant/insect responses, but the precise roles of environmental triggers and specific molecular components remain poorly defined. Aphid fecundity and plant responses were therefore measured in Arabidopsis thaliana mutants deficient in either catalase 2 (cat2), different protein phosphatase 2A (PP2A) subunits or glutathione (cad2, pad2, and clt1) under either moderate (250 μmol m s ) or high (800 μmol m s ) light. Aphid fecundity was decreased in pp2a-b'γ, cat2 and the cat2 pp2a-b'γ double mutants relative to the wild type under moderate irradiance. High light decreased aphid numbers in all genotypes except for cat2. Aphid fecundity was similar in the cat2 and glutathione-, phytoalexin-, and glucosinolate-deficient cat2cad2 double mutants under both irradiances. Aphid-induced increases in transcripts encoding the abscisic acid-related ARABIDOPSIS ZINC-FINGER PROTEIN 1 transcription factor were observed only under moderate light. Conversely, aphid induced increases in transcripts encoding the jasmonate-synthesis enzyme ALLENE OXIDE CYCLASE 3 was observed in all genotypes only under high light. Aphid-induced increases in REDOX RESPONSIVE TRANSCRIPTION FACTOR 1 mRNAs were observed in all genotypes except pp2a-b'ζ1-1 under both irradiances. Aphid fecundity is therefore regulated by cellular redox signalling that is mediated, at least in part, through PP2A-dependent mitochondria to nucleus signalling pathways.

摘要

氧化还原过程调节植物/昆虫的反应,但环境触发因素和特定分子成分的确切作用仍未得到明确界定。因此,在中度(250 μmol m s)或高光(800 μmol m s)下,在拟南芥突变体中测量了过氧化氢酶 2(cat2)、不同蛋白磷酸酶 2A(PP2A)亚基或谷胱甘肽(cad2、pad2 和 clt1)缺陷的拟南芥突变体中的蚜虫繁殖力和植物反应。与野生型相比,在中等光照下,pp2a-b'γ、cat2 和 cat2 pp2a-b'γ 双突变体中的蚜虫繁殖力降低。高光降低了所有基因型中的蚜虫数量,但 cat2 除外。在两种光照下,cat2 和谷胱甘肽、植物抗毒素和硫代葡萄糖苷缺乏的 cat2cad2 双突变体中的蚜虫繁殖力相似。只有在中等光照下,才观察到编码与脱落酸相关的拟南芥锌指蛋白 1 转录因子的转录物的蚜虫诱导增加。相反,只有在高光下,才观察到编码茉莉酸合成酶 ALLENE OXIDE CYCLASE 3 的转录物在所有基因型中均增加。只有在两种光照下,除了 pp2a-b'ζ1-1 之外,所有基因型中的 REDOX RESPONSIVE TRANSCRIPTION FACTOR 1 mRNAs 的蚜虫诱导增加。因此,蚜虫繁殖力受细胞氧化还原信号调节,至少部分通过 PP2A 依赖的线粒体到细胞核信号通路进行调节。

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