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两个结构相似的玉米胞质超氧化物歧化酶基因Sod4和Sod4A,对脱落酸和高渗胁迫的反应不同。

Two structurally similar maize cytosolic superoxide dismutase genes, Sod4 and Sod4A, respond differentially to abscisic acid and high osmoticum.

作者信息

Guan L, Scandalios J G

机构信息

Department of Genetics, Box 7614, North Carolina State University, Raleigh, North Carolina 27695-7614, USA.

出版信息

Plant Physiol. 1998 May;117(1):217-24. doi: 10.1104/pp.117.1.217.

Abstract

The maize (Zea mays) superoxide dismutase genes Sod4 and Sod4A are highly similar in structure but each responds differentially to environmental signals. We examined the effects of the hormone abscisic acid (ABA) on the developmental response of Sod4 and Sod4A. Although both Sod4 and Sod4A transcripts accumulate during late embryogenesis, only Sod4 is up-regulated by ABA and osmotic stress. Accumulation of Sod4 transcript in response to osmotic stress is a consequence of increased endogenous ABA levels in developing embryos. Sod4 mRNA is up-regulated by ABA in viviparous-1 mutant embryos. Sod4 transcript increases within 4 h with ABA not only in developing embryos but also in mature embryos and in young leaves. Sod4A transcript is up-regulated by ABA only in young leaves, but neither Sod4 nor Sod4A transcripts changed in response to osmotic stress. Our data suggest that in leaves Sod4 and Sod4A may respond to ABA and osmotic stress via alternate pathways. Since the Sod genes have a known function, we hypothesize that the increase in Sod mRNA in response to ABA is due in part to ABA-mediated metabolic changes leading to changes in oxygen free radical levels, which in turn lead to the induction of the antioxidant defense system.

摘要

玉米(Zea mays)超氧化物歧化酶基因Sod4和Sod4A在结构上高度相似,但对环境信号的反应各不相同。我们研究了激素脱落酸(ABA)对Sod4和Sod4A发育反应的影响。尽管Sod4和Sod4A转录本在胚胎发育后期都会积累,但只有Sod4会被ABA和渗透胁迫上调。发育中的胚胎内源性ABA水平升高导致Sod4转录本在渗透胁迫下积累。Sod4 mRNA在 viviparous-1突变体胚胎中被ABA上调。Sod4转录本不仅在发育中的胚胎中,而且在成熟胚胎和幼叶中,在4小时内随着ABA增加。Sod4A转录本仅在幼叶中被ABA上调,但Sod4和Sod4A转录本对渗透胁迫均无变化。我们的数据表明,在叶片中,Sod4和Sod4A可能通过不同途径对ABA和渗透胁迫作出反应。由于Sod基因具有已知功能,我们推测Sod mRNA对ABA的增加部分归因于ABA介导的代谢变化,导致氧自由基水平改变,进而导致抗氧化防御系统的诱导。

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