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MYBD employed by HY5 increases anthocyanin accumulation via repression of MYBL2 in Arabidopsis

Authors
Nguyen Hoai NguyenJeong, Chan YoungKang, Geun-HoYoo, Sang-DongHong, Suk-WhanLee, Hojoung
Issue Date
12월-2015
Publisher
WILEY
Keywords
MYBD (AT1G70000); anthocyanin; cytokinin; MYBL2 (AT1G71030); photomorphogenesis; histone acetylation; Arabidopsis thaliana
Citation
PLANT JOURNAL, v.84, no.6, pp.1192 - 1205
Indexed
SCIE
SCOPUS
Journal Title
PLANT JOURNAL
Volume
84
Number
6
Start Page
1192
End Page
1205
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/91804
DOI
10.1111/tpj.13077
ISSN
0960-7412
Abstract
Photomorphogenesis is an essential program in plant development. This process is effected by the balanced cooperation of many factors under light and dark conditions. In a previous study, we showed that MYB hypocotyl elongation-related (MYBH) is involved in cell elongation. To expand our understanding of MYBH function, we performed a yeast two-hybrid assay and identified an MYB-like Domain transcription factor (MYBD). In this study, we investigated the function of MYBD, which is an MYBH homolog involved in anthocyanin accumulation. MYBD expression increased in response to light or cytokinin, and MYBD enhanced anthocyanin biosynthesis via repression of MYBL2, which encodes a transcription factor that has a negative effect on this process. In addition, MYBD binding in vivo to the MYBL2 promoter and the lower level of histone H3K9 acetylation at the upstream region of MYBL2 in MYBD over-expressing plants in comparison with wild-type plants imply that MYBD represses MYBL2 expression via an epigenetic mechanism. HY5 directly binds to the MYBD promoter, which indicates that MYBD acts on HY5-downstream in light-or cytokinintriggered signaling pathways, leading to anthocyanin accumulation. Our results suggest that, although MYBD and MYBH are homologs, they act in opposite ways during plant photomorphogenesis, and these functions should be examined in further studies.
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