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转录组范围内WRKY转录因子的鉴定及其参与洋地黄苷生物合成的功能表征 。 (你提供的原文中“in.”后面似乎信息不完整)

Transcriptome-Wide Identification of WRKY Transcription Factor and Functional Characterization of Involved in Acteoside Biosynthesis in .

作者信息

Wang Fengqing, Li Xinrong, Zuo Xin, Li Mingming, Miao Chunyan, Zhi Jingyu, Li Yajing, Yang Xu, Liu Xiangyang, Xie Caixia

机构信息

College of Agronomy, Henan Agricultural University, Zhengzhou, China.

School of Medicine, Henan University of Chinese Medicine, Zhengzhou, China.

出版信息

Front Plant Sci. 2021 Sep 29;12:739853. doi: 10.3389/fpls.2021.739853. eCollection 2021.

Abstract

WRKYs play important roles in plant metabolism, but their regulation mechanism in remains elusive. In this study, 37 putative WRKY transcription factors (TFs) with complete WRKY domain from transcriptome sequence data were identified. Based on their conserved domains and zinc finger motif, the WRKY TFs were divided into five groups. Structural feature analysis shows that the 37 RgWRKY proteins contain WRKYGQK/GKK domains and a C2H2/C2HC-type zinc finger structure. To identify the function of members involved in acteoside biosynthesis, transcriptional profiles of 37 in hairy roots under salicylic acid (SA), methyl jasmonate (MeJA), and hydrogen peroxide (HO) treatments were systematically established using RNA-seq analysis. Based on the correlationship between the expression levels of genes and acteoside content, , , , , and were suggested to be involved in acteoside biosynthesis in , and was selected for gene functional research. Overexpression of increased the content of acteoside and total phenylethanoid glycosides (PhGs) in hairy roots and enhanced the transcript abundance of seven enzyme genes involved in the acteoside biosynthesis pathway. These results strongly suggest the involvement of the WRKY transcription factor in the regulation of acteoside biosynthesis.

摘要

WRKY转录因子在植物代谢中发挥重要作用,但其在[具体植物名称未给出]中的调控机制仍不清楚。在本研究中,从[具体植物名称未给出]转录组序列数据中鉴定出37个具有完整WRKY结构域的假定WRKY转录因子(TFs)。基于其保守结构域和锌指基序,将这些WRKY TFs分为五组。结构特征分析表明,37个RgWRKY蛋白含有WRKYGQK/GKK结构域和C2H2/C2HC型锌指结构。为了鉴定参与毛蕊花糖苷生物合成的成员的功能,利用RNA测序分析系统地建立了37个[具体植物名称未给出]在水杨酸(SA)、茉莉酸甲酯(MeJA)和过氧化氢(H₂O₂)处理下毛状根中的转录谱。基于基因表达水平与毛蕊花糖苷含量之间的相关性,[具体基因名称未给出]被认为参与了[具体植物名称未给出]中毛蕊花糖苷的生物合成,并选择[具体基因名称未给出]进行基因功能研究。[具体基因名称未给出]的过表达增加了毛状根中毛蕊花糖苷和总苯乙醇苷(PhGs)的含量,并提高了参与毛蕊花糖苷生物合成途径的7个酶基因的转录丰度。这些结果有力地表明WRKY转录因子参与了毛蕊花糖苷生物合成的调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b86c/8511629/c8b82135fe47/fpls-12-739853-g001.jpg

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