Boubakri Hatem, Chihaoui Saif-Allah, Najjar Eya, Barhoumi Fathi, Jebara Moez
Laboratory of Legumes and Sustainable Agrosystems, Centre of Biotechnology of Borj-Cedria, BP 901, 2050 Hammam-Lif, Tunisia.
3 Biotech. 2022 Aug;12(8):175. doi: 10.1007/s13205-022-03246-8. Epub 2022 Jul 16.
Peroxiredoxins (Prxs) are novel cysteine-based peroxidases which are involved in protecting cells from oxidative damage by catalyzing the reduction of different peroxides. The present study addressed, for the first time, genome-wide identification, evolutionary patterns and expression dynamics of gene family (). Nine Prx proteins were identified in based on homology searches. The phylogeny analysis of Prxs from seven plant species revealed that Prx proteins can be clustered into four groups (1C-Prx, 2C-Prxs, PrxQ and type II Prxs). Both tandem and segmental duplication contributed to gene family expansion. Intragenic reorganizations including gain/loss of exon/intron and insertions/deletions have also contributed to gene diversification. The collinearity analysis revealed the presence of some orthologous gene pairs between and genomes. The Ka/Ks ratio indicated that two of the three duplicated gene pairs have undergone a purifying selection. Redundant stress-related cis-acting elements were also found in the promoters of most genes. RT q-PCR analysis revealed an upregulation of key members in response to symbiosis and different abiotic factors. The upregulation of targeted members, particularly in leaves exposed to salinity or drought, was accompanied by an accumulation of hydrogen peroxide (HO). When exogenously applied, HO modulated almost all genes, suggesting a potential HO-scavenging role for these proteins. Collectively, our analysis provided valuable information for further functional analysis of key members to improve common bean stress tolerance and/or its symbiotic performance.
The online version contains supplementary material available at 10.1007/s13205-022-03246-8.
过氧化物酶(Prxs)是一类新型的基于半胱氨酸的过氧化物酶,通过催化不同过氧化物的还原参与保护细胞免受氧化损伤。本研究首次对基因家族进行了全基因组鉴定、进化模式和表达动态分析。基于同源性搜索在[研究对象]中鉴定出9种Prx蛋白。对来自7种植物的Prxs进行系统发育分析表明,Prx蛋白可分为4组(1C-Prx、2C-Prxs、PrxQ和II型Prxs)。串联重复和片段重复都促成了基因家族的扩张。包括外显子/内含子的获得/丢失以及插入/缺失在内的基因内重组也促成了基因的多样化。共线性分析揭示了[研究对象]和[对比对象]基因组之间存在一些直系同源基因对。Ka/Ks比值表明,三个重复基因对中的两个经历了纯化选择。在大多数基因的启动子中也发现了冗余的胁迫相关顺式作用元件。RT-qPCR分析表明,关键基因成员在共生和不同非生物因子作用下上调。靶向基因成员的上调,特别是在暴露于盐度或干旱的叶片中,伴随着过氧化氢(H₂O₂)的积累。当外源施加时,H₂O₂调节几乎所有基因,表明这些蛋白具有潜在的H₂O₂清除作用。总体而言,我们的分析为进一步对关键基因成员进行功能分析提供了有价值的信息,以提高普通菜豆的胁迫耐受性和/或其共生性能。
在线版本包含可在10.1007/s13205-022-03246-8获取的补充材料。