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Genome-wide analysis of PHD finger gene family and identification of potential miRNA and their PHD finger gene specific targets in

机译:基因组分析PHD手指基因家族及潜在miRNA的鉴定及其PHD手指基因特异性靶标

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摘要

Rice (Oryza sativa L.) is one of the most important cereal crops for one third of the world population. However, the grain quality as well as yield of rice is severely affected by various abiotic stresses. Environmental stresses affect the expression of various microRNAs (miRNAs) which in turn negatively regulate gene expression at the post-transcriptional level either by degrading the target mRNA genes or suppressing translation in plants. Plant homeo-domain (PHD) finger proteins are known to be involved in the plant response to salinity stress. In the present study, we identified 44 putative OsPHD finger genes in Oryza sativa Indica, using Ensembl Plants Database. Using computational approach, potential miRNAs that target OsPHD finger genes were identified. Out of the 44 OsPHD finger genes only three OsPHD finger genes i.e., OsPHD2, OsPHD35 and OsPHD11, were found to be targeted by five newly identified putative miRNAs i.e., ath-miRf10010-akr, ath-miRf10110-akr, osa-miR1857–3p, osa-miRf10863-akr, and osa-miRf11806-akr. This is the first report of these five identified miRNAs on targeting PHD finger in Oryza sativa Indica. Further, expression analysis of 44 PHD finger genes under salinity was also performed using quantitative Real-Time PCR. The expression profile of 8 genes were found to be differentially regulated, among them two genes were significantly up regulated i.e., OsPHD6 and OsPHD12. In silico protein-protein interaction analysis using STRING database showed interaction of the OsPHD finger proteins with other protein partners that are directly or indirectly involved in development and abiotic stress tolerance.
机译:米(Oryza sativa L.)是世界三分之一的谷物作物之一。然而,谷物质量以及水稻产量受到各种非生物应激的严重影响。环境应力影响各种MicroRNA(miRNA)的表达,其通过使靶mRNA基因降解植物中的靶mRNA基因或抑制翻译,递转在转录后水平处的基因表达。已知植物家庭结构域(PHD)手指蛋白涉及植物对盐度应力的反应。在本研究中,我们使用Ensembl植物数据库鉴定了Oryza Sativa Indema中的44个推定的磷散手基因。使用计算方法,鉴定了靶向静脉注射指导基因的潜在miRNA。在44μSOphd指基因中仅发现三个磷基因基因,即溶液,溶液35和散氨酸,靶向5个新鉴定的推定miRNA,即Ath-MiRF10010-AKR,Ath-MiRF10110-AKR,OSA-MIR1857-3P ,OSA-MIRF10863-AKR和OSA-MIRF11806-AKR。这是本五个鉴定的miRNA对靶向博士赛斯蒂加籼稻的第一报告。此外,还使用定量实时PCR进行盐度下进行44个Phd手指基因的表达分析。发现8个基因的表达谱被差异调节,其中两个基因显着调节I.,溶氨&00.在硅蛋白 - 蛋白质 - 蛋白质 - 蛋白质蛋白质相互作用分析中,使用弦数据库显示磷蛋白与其他蛋白质合作伙伴的相互作用直接或间接地参与开发和非生物胁迫耐受性。

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