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[光皮桦中miR164及其靶基因NAC1对低硝酸盐有效性响应的表达分析]

[Expression analysis of miR164 and its target gene NAC1 in response to low nitrate availability in Betula luminifera].

作者信息

Wu Jun, Zhang Jun-hong, Huang Meng-hui, Zhu Min-hui, Tong Zai-kang

出版信息

Yi Chuan. 2016 Feb;38(2):155-62. doi: 10.16288/j.yczz.15-231.

Abstract

Nitrogen, an essential macronutrient for the growth and development of plants, affects above- ground biomass accumulation dramatically. Thus, it is very important to reveal the molecular mechanisms of how plants resist or adapt to low nitrogen availability. The NAC1(NAM, ATAF, CUC 1) gene, located in the upstream regulatory network, has been reported to resist low nitrogen by regulating expression of key downstream genes and thus root growth in (Populus tremula × alba).In this study, we detected the responses of miR164 and its target gene NAC1 under nitrate-starvation condition using the Betula luminifera somaclones G49-3 as material. The NAC1 gene which contains 1497 bp sequence, encodes 358 amino acids and contains a highly conserved NAM domain at N terminal was cloned by the RACE method. The NAC1 was then validated to be the target gene of miR164 via 5'-RACE, and the cleavage site was between the 10(th) and 11(th) base. The expression patterns of miR164 and its target gene NAC1 were further detected under nitrate-starvation condition through qRT-PCR analysis. The results showed that miR164 expression was repressed by nitrate-starvation at the beginning of the treatment (4 d) and then ascended. However, the expression pattern of miR164 in roots was different from that in shoots and leaves. Moreover, the expression levels of target gene NAC1 and miR164 were negatively correlated. The expression level of miR164 in root was increased while that of NAC1 was decreased under Re treatment, which indicated that miR164 and its target gene NAC1 play a regulatory role in response to low nitrate availability. The findings of our study may help elucidate the molecular mechanisms by which miR164 regulates target gene NAC1 at post-transcriptional level, and provide valuable information for further study of the regulatory roles of miR164-NAC1 under nitrate-starvation condition.

摘要

氮是植物生长发育所必需的大量元素,对地上生物量的积累有显著影响。因此,揭示植物抵抗或适应低氮环境的分子机制非常重要。据报道,位于上游调控网络中的NAC1(NAM、ATAF、CUC 1)基因通过调节关键下游基因的表达从而影响(银白杨)根系生长,进而抵抗低氮环境。在本研究中,我们以光皮桦体细胞无性系G49 - 3为材料,检测了硝酸盐饥饿条件下miR164及其靶基因NAC1的响应。通过RACE方法克隆了包含1497 bp序列、编码358个氨基酸且在N端含有高度保守NAM结构域的NAC1基因。随后通过5'-RACE验证NAC1是miR164的靶基因,切割位点位于第10和第11个碱基之间。通过qRT-PCR分析进一步检测了硝酸盐饥饿条件下miR164及其靶基因NAC1的表达模式。结果表明,在处理开始时(4天),硝酸盐饥饿抑制了miR164的表达,随后其表达量上升。然而,miR164在根中的表达模式与茎和叶不同。此外,靶基因NAC1和miR164的表达水平呈负相关。在再处理条件下,根中miR164的表达水平升高而NAC1的表达水平降低,这表明miR164及其靶基因NAC1在响应低硝酸盐环境中发挥调节作用。我们的研究结果可能有助于阐明miR164在转录后水平调控靶基因NAC1的分子机制,并为进一步研究硝酸盐饥饿条件下miR164 - NAC1的调控作用提供有价值的信息。

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