Ectopic Expression of a R2R3-MYB Transcription Factor Gene LjaMYB12 from Lonicera japonica Increases Flavonoid Accumulation in Arabidopsis thaliana

Thunb. is a widely used medicinal plant and is rich in a variety of active ingredients. Flavonoids are one of the important components in and their content is an important indicator for evaluating the quality of this herb. To study the regulation of flavonoid biosynthesis in , an R2R3-MYB transcript...

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Veröffentlicht in:International journal of molecular sciences 2019-09, Vol.20 (18), p.4494
Hauptverfasser: Qi, Xiwu, Fang, Hailing, Chen, Zequn, Liu, Zhiqi, Yu, Xu, Liang, Chengyuan
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Sprache:eng
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Zusammenfassung:Thunb. is a widely used medicinal plant and is rich in a variety of active ingredients. Flavonoids are one of the important components in and their content is an important indicator for evaluating the quality of this herb. To study the regulation of flavonoid biosynthesis in , an R2R3-MYB transcription factor gene was isolated and characterized. Bioinformatics analysis indicated that belonged to the subgroup 7, with a typical R2R3 DNA-binding domain and conserved subgroup 7 motifs. The transcriptional level of was proportional to the total flavonoid content during the development of flowers. Subcellular localization analysis revealed that LjaMYB12 localized to the nucleus. Transactivation activity assay indicated that LjaMYB12 was a transcriptional activator. Then, ectopic expression of in Arabidopsis could increase PAL activity and flavonoid content and promote transcription of a range of flavonoid biosynthetic genes. Interestingly, the fold changes of downstream genes in the flavonoid biosynthetic pathway were significantly higher than that of the upstream genes, which suggested that may have different regulatory patterns for the upstream and downstream pathways of flavonoid biosynthesis. The results provided here will effectively facilitate the study of subgroup 7 MYBs and transcriptional regulation of flavonoid biosynthesis in .
ISSN:1422-0067
1661-6596
1422-0067
DOI:10.3390/ijms20184494