首页> 外文期刊>Journal of Plant Growth Regulation >Genome-Wide Identification and Expression Profiling of Ascorbate Peroxidase (APX) and Glutathione Peroxidase (GPX) Genes Under Drought Stress in Sorghum (Sorghum bicolor L.)
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Genome-Wide Identification and Expression Profiling of Ascorbate Peroxidase (APX) and Glutathione Peroxidase (GPX) Genes Under Drought Stress in Sorghum (Sorghum bicolor L.)

机译:抗坏血酸过氧化物酶(APX)和谷胱甘肽过氧化物酶(GPX)基因在高粱(高粱双色L.)下抗坏血酸过氧化物酶(APX)和谷胱甘肽过氧化物酶(GPX)基因的基因组鉴定及表达分析

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摘要

APX and GPX are two crucial plant antioxidant enzymes. By protein homology search, nine APX and seven GPX members were identified in Sorghum bicolor genome. They were annotated based on chromosomal localizations as SbAPX1-9 and SbGPX1-7. APXs were distributed on six Sorghum chromosomes and encoded polypeptides of 250-474 residues with characteristic "peroxidase" domain, whereas GPXs were on five chromosomes and encoded proteins of 136-232 residues characterized by a "GSHPx" domain. The first about 1-90 amino acid residues in SbAPXs and about 60-70 amino acid residues in SbGPXs from N-terminus corresponded to transit peptides, and formed the main source of sequence variations. On the other hand, APXs/GPXs appeared to be significantly conserved at the amino acid sequence level. Residues in active and/or metal binding sites of these enzymes were also revealed with inference to their Arabidopsis counterparts. The combined Sorghum-Arabidopsis APX and GPX phylogenies allowed inferring functional roles to putative Sorghum sequences at cross-species level. In digital RNA-seq data from Sorghum, APXs within sensitive genotypes were relatively more responsive to drought compared to GPXs. Differentially upregulated APX4 and downregulated GPX2 suggested that their performance was synergistic. SbAPXs/GPXs expression in drought-exposed sorghum roots and leaves were quantified by Real-Time quantitative PCR (RT-qPCR). Drought-exposed plants morphologically demonstrated reductions in stem/root elongation and size, retardation in plant growth, and erected leaves. Expressions of APXs/GPXs were mostly upregulated in aboveground parts of drought-exposed plants, e.g., leaves while they were downregulated in roots. Furthermore, APX1 and APX5 in leaves, and APX8, APX9, GPX5, and GPX6 in roots showed significant changes in expression levels; therefore, their synergetic regulation during drought should be considered.
机译:APX和GPX是两个关键的植物抗氧化酶。通过蛋白质同源性搜索,在高粱双色基因组中鉴定了九个APX和七个GPX成员。它们根据SBAPX1-9和SBGPX1-7基于染色体局部注释。 APXS在六个高粱染色体上分布,并编码了250-474个残基的多肽,具有特征“过氧化物酶”结构域,而GPX是在五种染色体上,并编码136-232残基的蛋白质,其特征在于“GSHPX”结构域。 SBAPX中的第一个约1-90个氨基酸残基与来自N-末端的SBGPX中的约60-70氨基酸残基对应于过渡肽,形成序列变化的主要来源。另一方面,APXS / GPX似乎在氨基酸序列水平上显着保守。也揭示了这些酶的活性和/或金属结合位点的残基对其拟南芥对应物揭示。合并的高粱 - 拟南芥APX和GPX文学允许在交叉物种水平下推断出推定高粱序列的功能作用。在来自高粱的数字RNA-SEQ数据中,与GPX相比,敏感基因型内的APX对干旱相对较多。差异上调的APX4和下调的GPX2表明它们的表现是协同作用。通过实时定量PCR(RT-QPCR)量化干旱暴露高粱根和叶中的SBAPX / GPX表达。干旱暴露的植物形态学上证明了茎/根伸长和尺寸的减少,植物生长的延迟,并竖立叶片。 APXS / GPX的表达大多上调在干旱暴露植物的地上,例如,叶片在根中下降。此外,叶片中的APX1和APX5和ROOTS中的APX8,APX9,GPX5和GPX6显示出表达水平的显着变化;因此,应考虑干旱期间的协同监管。

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