郭志英, 李卿, 吴循循, 陈军峰, 黄玉香, 马晓娟, 刁勇, 张磊. 马蓝WRKY转录因子家族生物信息学及表达特征分析J. 药学学报, 2022, 57(9): 2864-2875. DOI: 10.16438/j.0513-4870.2022-0433
引用本文: 郭志英, 李卿, 吴循循, 陈军峰, 黄玉香, 马晓娟, 刁勇, 张磊. 马蓝WRKY转录因子家族生物信息学及表达特征分析J. 药学学报, 2022, 57(9): 2864-2875. DOI: 10.16438/j.0513-4870.2022-0433
GUO Zhi-ying, LI Qing, WU Xun-xun, CHEN Jun-feng, HUANG Yu-xiang, MA Xiao-juan, DIAO Yong, ZHANG Lei. Bioinformatics and expressional analysis of WRKY transcription factor family in Baphicacanthus cusiaJ. Acta Pharmaceutica Sinica, 2022, 57(9): 2864-2875. DOI: 10.16438/j.0513-4870.2022-0433
Citation: GUO Zhi-ying, LI Qing, WU Xun-xun, CHEN Jun-feng, HUANG Yu-xiang, MA Xiao-juan, DIAO Yong, ZHANG Lei. Bioinformatics and expressional analysis of WRKY transcription factor family in Baphicacanthus cusiaJ. Acta Pharmaceutica Sinica, 2022, 57(9): 2864-2875. DOI: 10.16438/j.0513-4870.2022-0433

马蓝WRKY转录因子家族生物信息学及表达特征分析

Bioinformatics and expressional analysis of WRKY transcription factor family in Baphicacanthus cusia

  • 摘要: WRKY转录因子是植物中一类保守的转录因子, 在植物生长发育和次生代谢过程中发挥重要的调控作用。本研究对马蓝(Baphicacanthus cusia) 不同组织(根、茎和叶) 的转录组数据进行分析, 共鉴定了65个马蓝WRKY (BcWRKY) 家族成员。其编码氨基酸长度约为221~706 aa, 等电点为4.68~9.68, 分子质量为25 711.8~75 475 Da, 二级结构主要为无规则卷曲, 亚细胞定位预测显示多数BcWRKYs定位在细胞核中。系统进化分析将其分为3大族, 其中第二大族(Group II) 又可分为5个亚族(Group IIa、Group IIb、Group IIc、Group IId和Group IIe)。结构域分析显示BcWRKY均含有高度保守的WRKYGQK基序。利用实时荧光定量PCR (RT-PCR) 对马蓝根、茎和叶中高表达的10个WRKY基因进行检测, 发现均可响应脱落酸(abscisic acid, ABA)、茉莉酸甲酯(methyl jasmonate, MeJA) 和水杨酸(salicylic acid, SA) 的诱导。本研究为进一步阐明马蓝中吲哚生物碱生物合成中WRKY转录因子的分子机制提供基础。

     

    Abstract: WRKY, a class of conserved transcription factors in plants, plays important roles in plant growth, development and secondary metabolism. In the present study, 65 WRKY members were identified from de novo transcriptome sequencing data of three different tissues (root, stems and leaves) of Baphicacanthus cusia. BcWRKY proteins contained from 221 to 706 amino acids and the isoelectric point is from 4.68 to 9.68. Molecular weights range from 25 711.8 to 75 475 Da. The main secondary structures of BcWRKYs protein are random coil. A subcellular localization prediction indicated that the putative BcWRKY proteins were enriched in the nuclear region. Phylogenetic analysis showed that BcWRKYs could be categorized into three groups and five subgroups (Group IIa, Group IIb, Group IIc, Group IId and Group IIe) in Group II. Structural analysis found that all BcWRKY proteins contained a highly conserved motif WRKYGQK. Finally, the transcriptional profiles of ten BcWRKY genes highly expressed in root, stem and leaf tissues under abscisic acid (ABA), methyl jasmonate (MeJA), or salicylic acid (SA) treatment were systematically investigated using qRT-PCR analysis. Results showed that a total of ten BcWRKY genes were differentially expressed in response to ABA, MeJA, and SA treatment. This work would be provided a basis for further elucidating the molecular mechanism of WRKY transcription factors in the biosynthesis of indole alkaloids in B. cusia.

     

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