Transcriptome-Wide Identification and Characterization of the JAZ Gene Family in Mentha canadensis L.

茉莉酸 生物 茉莉酸甲酯 拟南芥 茉莉酸 基因 基因家族 转录组 脱落酸 遗传学 亚细胞定位 蛋白质结构域 基因表达 突变体
作者
Dongbei Xu,Yong Ma,Tengfei Qin,Wu‐Neng Tang,Xiwu Qi,Xia Wang,Rui-Cen Liu,Hailing Fang,Zequn Chen,Chengyuan Liang,Wei Wu
出处
期刊:International Journal of Molecular Sciences [MDPI AG]
卷期号:22 (16): 8859-8859 被引量:7
标识
DOI:10.3390/ijms22168859
摘要

Jasmonate ZIM-domain (JAZ) proteins are the crucial transcriptional repressors in the jasmonic acid (JA) signaling process, and they play pervasive roles in plant development, defense, and plant specialized metabolism. Although numerous JAZ gene families have been discovered across several plants, our knowledge about the JAZ gene family remains limited in the economically and medicinally important Chinese herb Mentha canadensis L. Here, seven non-redundant JAZ genes named McJAZ1–McJAZ7 were identified from our reported M. canadensis transcriptome data. Structural, amino acid composition, and phylogenetic analysis showed that seven McJAZ proteins contained the typical zinc-finger inflorescence meristem (ZIM) domain and JA-associated (Jas) domain as conserved as those in other plants, and they were clustered into four groups (A-D) and distributed into five subgroups (A1, A2, B1, B2, and D). Quantitative real-time PCR (qRT-PCR) analysis showed that seven McJAZ genes displayed differential expression patterns in M. canadensis tissues, and preferentially expressed in flowers. Furthermore, the McJAZ genes expression was differentially induced after Methyl jasmonate (MeJA) treatment, and their transcripts were variable and up- or down-regulated under abscisic acid (ABA), drought, and salt treatments. Subcellular localization analysis revealed that McJAZ proteins are localized in the nucleus or cytoplasm. Yeast two-hybrid (Y2H) assays demonstrated that McJAZ1-5 interacted with McCOI1a, a homolog of Arabidopsis JA receptor AtCOI1, in a coronatine-dependent manner, and most of McJAZ proteins could also form homo- or heterodimers. This present study provides valuable basis for functional analysis and exploitation of the potential candidate McJAZ genes for developing efficient strategies for genetic improvement of M. canadensis.
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