鉴定对 MeJA 有反应的转录因子基因,确定 LaMYC2 转录因子对 Lycoris aurea 中番茄碱生物合成的正向调控特性

IF 4 3区 生物学 Q1 PLANT SCIENCES
Zhe Zhou , Mingzhu Wu , Bin Sun , Jie Li , Junde Li , Zhengtai Liu , Meng Gao , Lei Xue , Sheng Xu , Ren Wang
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引用次数: 0

摘要

茉莉酸盐(JAs)是主要的植物激素之一,调节植物的生长发育、胁迫反应和次生代谢。作为 JA 信号通路的主要调节因子,MYC2 在植物次生代谢产物的合成和积累中也发挥着重要作用。在本研究中,我们对不同处理时间的茉莉酸甲酯(MeJA)幼苗进行了转录组比较分析。通过 RNA 测序共鉴定出 31,193 个差异表达基因(DEGs)。其中,732个差异表达的转录因子(TFs)被鉴定,包括51个TF家族。数量最多的转录因子家族是WRKY蛋白(80个),其次是AP2/ERF-EFR(67个)、MYB(59个)、bHLH(52个)和NAC蛋白(49个)家族。随后,通过计算TF DEGs表达水平与番茄红素含量之间的皮尔逊相关系数(PCC),确定了41个参与番茄红素积累的潜在TF基因(|PCC| >0.8),包括36个正调控因子和5个负调控因子。此外,还根据转录组测序克隆了一个 MeJA 诱导基因(即 )。生物信息学分析表明,LaMYC2 蛋白含有 bHLH-MYC_N 结构域和 bHLH-AtAIB_like motif。LaMYC2蛋白定位于细胞核中,并能部分挽救.MYC2突变体。LaMYC2 蛋白能与之前发现的大多数 LaJAZs(尤其是 LaJAZ3 和 LaJAZ4)相互作用。花瓣中番茄红素含量的瞬时过表达增加,可能与()和()基因转录水平的激活有关。通过分离Ⅳ的起始密码子(ATG)上游887 bp长的启动子片段,我们发现Ⅴ的启动子中存在几种不同类型的E-box基序(CANNTG)。 进一步研究表明,LaMYC2确实能与启动子中的E-box(CACATG)结合,验证了参与番茄红素生物合成的途径基因可受LaMYC2调控,LaMYC2在番茄红素生物合成的调控中具有积极作用。这些研究结果表明,LaMYC2 是番茄碱生物合成的正向调控因子,可促进对该基因的进一步功能研究,特别是其在藜科植物生物碱积累中的潜在调控作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of transcription factor genes responsive to MeJA and characterization of a LaMYC2 transcription factor positively regulates lycorine biosynthesis in Lycoris aurea

Jasmonates (JAs) are among the main phytohormones, regulating plant growth and development, stress responses, and secondary metabolism. As the major regulator of the JA signaling pathway, MYC2 also plays an important role in plant secondary metabolite synthesis and accumulation. In this study, we performed a comparative transcriptome analysis of Lycoris aurea seedlings subjected to methyl jasmonate (MeJA) at different treatment times. A total of 31,193 differentially expressed genes (DEGs) were identified by RNA sequencing. Among them, 732 differentially expressed transcription factors (TFs) comprising 51 TF families were characterized. The most abundant TF family was WRKY proteins (80), followed by AP2/ERF-EFR (67), MYB (59), bHLH (52), and NAC protein (49) families. Subsequently, by calculating the Pearson's correlation coefficient (PCC) between the expression level of TF DEGs and the lycorine contents, 41 potential TF genes (|PCC| >0.8) involved in lycorine accumulation were identified, including 36 positive regulators and 5 negative regulators. Moreover, a MeJA-inducible MYC2 gene (namely LaMYC2) was cloned on the basis of transcriptome sequencing. Bioinformatic analyses revealed that LaMYC2 proteins contain the bHLH-MYC_N domain and bHLH-AtAIB_like motif. LaMYC2 protein is localized in the cell nucleus, and can partly rescue the MYC2 mutant in Arabidopsis thaliana. LaMYC2 protein could interact with most LaJAZs (especially LaJAZ3 and LaJAZ4) identified previously. Transient overexpression of LaMYC2 increased lycorine contents in L. aurea petals, which might be associated with the activation of the transcript levels of tyrosine decarboxylase (TYDC) and phenylalanine ammonia lyase (PAL) genes. By isolating the 887-bp-length promoter fragment upstream of the start codon (ATG) of LaTYDC, we found several different types of E-box motifs (CANNTG) in the promoter of LaTYDC. Further study demonstrated that LaMYC2 was indeed able to bind the E-box (CACATG) present in the LaTYDC promoter, verifying that the pathway genes involved in lycorine biosynthesis could be regulated by LaMYC2, and that LaMYC2 has positive roles in the regulation of lycorine biosynthesis. These findings demonstrate that LaMYC2 is a positive regulator of lycorine biosynthesis and may facilitate further functional research of the LaMYC2 gene, especially its potential regulatory roles in Amaryllidaceae alkaloid accumulation in L. aurea.

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来源期刊
Journal of plant physiology
Journal of plant physiology 生物-植物科学
CiteScore
7.20
自引率
4.70%
发文量
196
审稿时长
32 days
期刊介绍: The Journal of Plant Physiology is a broad-spectrum journal that welcomes high-quality submissions in all major areas of plant physiology, including plant biochemistry, functional biotechnology, computational and synthetic plant biology, growth and development, photosynthesis and respiration, transport and translocation, plant-microbe interactions, biotic and abiotic stress. Studies are welcome at all levels of integration ranging from molecules and cells to organisms and their environments and are expected to use state-of-the-art methodologies. Pure gene expression studies are not within the focus of our journal. To be considered for publication, papers must significantly contribute to the mechanistic understanding of physiological processes, and not be merely descriptive, or confirmatory of previous results. We encourage the submission of papers that explore the physiology of non-model as well as accepted model species and those that bridge basic and applied research. For instance, studies on agricultural plants that show new physiological mechanisms to improve agricultural efficiency are welcome. Studies performed under uncontrolled situations (e.g. field conditions) not providing mechanistic insight will not be considered for publication. The Journal of Plant Physiology publishes several types of articles: Original Research Articles, Reviews, Perspectives Articles, and Short Communications. Reviews and Perspectives will be solicited by the Editors; unsolicited reviews are also welcome but only from authors with a strong track record in the field of the review. Original research papers comprise the majority of published contributions.
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