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Aromatic amino acids biosynthesis genes identification and expression analysis under salt and drought stresses in Solanum lycopersicum L.

机译:Solanum Lycopersicum L中盐和干旱胁迫下芳族氨基酸生物合成基因鉴定及表达分析。

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摘要

Aromatic amino acids (AAA), phenylalanine (Phe), tyrosine (Tyr) and tryptophan (Trp), are essential molecules in the plant metabolism. In this study, three AAA biosynthesis genes, chorismate synthase (CS), chorismate mutase (CM) and anthranilate synthase (AS), were identified in genome-wide scale in tomato (Solanum lycopersicum) genome. Also, bioinformatics analyses including sequence and phylogenetic analyses, predicted microRNAs targeting, digital expression and co-expression analyses and seconder and tertiary structure analyses of AAA proteins were performed. The expressions of AAA genes under drought and salt stresses were evaluated using Real Time-quantitative PCR (RT-qPCR). The promotor sequence analyses of the genes showed the presence of diverse cis-regularity elements, including light responsive, hormone responsiveness, heat stress responsiveness and elicitor-responsive elements. Based on the digital expression data, CS1 is more consistently expressed over CM1 and ASA1 through developmental stages in tomato. Co-expression network analyses revealed complex interactions between AAA genes and genes in other metabolic pathways. The expressions of AAA genes fluctuated between 0.93-2.23 fold under drought and salt stresses. Over all, it can be proposed that data obtained from this study could contribute to identification and functions of AAA genes under abiotic stress conditions for plants, particularly tomato.
机译:芳族氨基酸(AAA),苯丙氨酸(PHE),酪氨酸(TYR)和色氨酸(TRP)是植物代谢中的必需分子。在该研究中,以番茄(Solanum Lycopersicum)基因组的基因组 - 范围为基因组尺度,鉴定了三种AAA生物合成基因,酸酸合酶(Cs),酸酸酯异位异质(CM)和邻苯胺合酶(AS)。此外,在包括序列和系统发育分析,预测的MicroRNA靶向,数字表达和共表达分析以及SEAA蛋白的二级结构分析的生物信息学分析。使用实时定量PCR(RT-QPCR)评估干旱和盐胁迫下AAA基因的表达。该基因的促进序列分析显示了不同的顺式规则性元素,包括光响应性,激素响应性,热应激响应性和Elicitor响应性元件。基于数字表达数据,CS1通过番茄中的发育阶段更始终如一地表达CM1和ASA1。共表达网络分析显示了其他代谢途径中AAA基因和基因之间的复杂相互作用。在干旱和盐胁迫下,AAA基因的表达波动波动在0.93-2.23折之间。总之,可以提出从本研究中获得的数据可以有助于植物,特别是番茄的非生物胁迫条件下的AAA基因的鉴定和功能。

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