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首页> 外文期刊>Plant Omics >Differential expression of kenaf phenylalanine ammonia-lyase (PAL) ortholog during developmental stages and in response to abiotic stresses
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Differential expression of kenaf phenylalanine ammonia-lyase (PAL) ortholog during developmental stages and in response to abiotic stresses

机译:洋麻苯丙氨酸解氨酶(PAL)直系同源物在发育阶段和响应非生物胁迫的差异表达

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Phenylalanine ammonia-lyase (PAL) is a key enzyme in the phenylpropanoid pathway. A full-length of the gene putatively encoding phenylalanine ammonia-lyase (PAL) was cloned from kenaf (Hibiscus cannabinus L.) using degenerate primers and the RACE (rapid amplification of cDNA ends) method. The full-length PAL ortholog in kenaf consists of a 2,148 bp open reading frame encoding 715 amino acids (JQ779022). The deduced amino acid sequence showed high similarity to those of PAL from Ricinus communis (88%) and Vitis vinifera (86%). The expression of the PAL transcript was examined in different tissues, developmental stages, and after treatments with abiotic stresses (wound, NaCl, cold, H2O2, ABA, SA, MeJA and drought) using quantitative real-time reverse transcriptase polymerase chain reaction (QPCR). The PAL ortholog was differentially expressed in the different tissues and developmental stages. The highest transcript level of the PAL ortholog was observed in young (4-week-old) stem and mature flower tissues, with a certain level of expression in all tissues and organs tested. Three-week-old kenaf stem tissues were used to evaluate the effects of abiotic stresses on PAL ortholog expression. The highest transcript level of the PAL ortholog was observed at an early time point (1 or 6 h) after treatments with wound (1 h), H2O2 (6 h) and SA (6 h), while the highest transcript level was detected at the late time point (24 h) after treatments with NaCl, cold and ABA. The PAL ortholog was not significantly induced by MeJA, while drought repressed the PAL ortholog.
机译:苯丙氨酸氨裂合酶(PAL)是苯丙烷途径中的关键酶。使用简并引物和RACE(cDNA末端的快速扩增)方法从洋麻(Hibiscus cannabinus L.)中克隆了假定编码苯丙氨酸氨解酶(PAL)的全长基因。洋麻中的全长PAL直向同源物由2,148 bp的开放阅读框组成,编码715个氨基酸(JQ779022)。推导的氨基酸序列显示出与来自蓖麻(88%)和葡萄(86%)的PAL具有高度相似性。使用定量实时逆转录酶聚合酶链反应(QPCR)在不同组织,发育阶段以及经过非生物胁迫(伤口,NaCl,寒冷,H2O2,ABA,SA,MeJA和干旱)处理后,检查了PAL转录的表达。 )。 PAL直向同源物在不同的组织和发育阶段中差异表达。在年轻(4周龄)茎和成熟花组织中观察到PAL直系同源物的最高转录水平,在所有测试的组织和器官中都有一定水平的表达。三周龄的洋麻干组织被用来评估非生物胁迫对PAL直向同源物表达的影响。在伤口(1 h),H2O2(6 h)和SA(6 h)处理后的早期时间点(1或6 h)观察到PAL直系同源物的最高转录水平,而在NaCl,冷水和ABA处理后的较晚时间点(24小时)。 MeJA没有明显诱导PAL直系同源物,而干旱抑制了PAL直系同源物。

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