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Isolation, expression and functional analysis of a putative RNA-dependent RNA polymerase gene from maize (Zea mays L.)

机译:玉米(Zea mays L.)推定的RNA依赖性RNA聚合酶基因的分离,表达及功能分析

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RNA-dependent RNA polymerases (RdRPs) in plants have been reported to be involved in post-transcriptional gene silencing (PTGS) and antiviral defense. In this report, an RdRP gene from maize (ZmRdRP1) was obtained by rapid amplification of cDNA ends (RACE) and RT-PCR. The mRNA of ZmRdRP1 was composed of 3785 nucleotides, including a 167 nt 5o untranslated region (UTR), a 291 nt 3oUTR and a 3327 nt open reading frame (ORF), which encodes a putative protein of 1108 amino acids with an estimated molecular mass of 126.9 kDa and a predicated isoelectric point (pI) of 8.37. Real-time quantitative RT-PCR analysis showed that ZmRdRP1 was elicited by salicylic acid (SA) treatment, methyl jasmonate (MeJA) treatment and sugarcane mosaic virus (SCMV) infection. We silenced ZmRdRP1 by constitutively expressing an inverted-repeat fragment of ZmRdRP1 (ir-RdRP1) in transgenic maize plants. Further studies revealed that the ir-RdRP1 transgenic plants were more susceptible to SCMV infection than wild type plants. Virus-infected transgenic maize plants developed more serious disease symptoms and accumulated more virus than wild type plants. These findings suggested that ZmRdRP1 was involved in antiviral defense in maize.
机译:据报道,植物中依赖RNA的RNA聚合酶(RdRPs)参与转录后基因沉默(PTGS)和抗病毒防御。在本报告中,通过快速扩增cDNA末端(RACE)和RT-PCR获得了来自玉米的RdRP基因(ZmRdRP1)。 ZmRdRP1的mRNA由3785个核苷酸组成,包括一个167 nt 5o非翻译区(UTR),一个291 nt 3oUTR和一个3327 nt开放阅读框(ORF),其编码一个推测的1108个氨基酸的蛋白质,估计的分子量126.9 kDa的等电点和8.37的预测等电点(pI)。实时定量RT-PCR分析表明,ZmRdRP1是由水杨酸(SA)处理,茉莉酸甲酯(MeJA)处理和甘蔗花叶病毒(SCMV)感染引起的。我们通过在转基因玉米植物中组成型表达ZmRdRP1的反向重复片段(ir-RdRP1)使ZmRdRP1沉默。进一步的研究表明,与野生型植物相比,ir-RdRP1转基因植物更容易受到SCMV感染。与野生型植物相比,病毒感染的转基因玉米植物表现出更严重的疾病症状并且积累了更多的病毒。这些发现表明ZmRdRP1参与了玉米的抗病毒防御。

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