Identification of a cis-acting regulatory motif recognized by MYB46, a master transcriptional regulator of secondary wall biosynthesis

被引:94
|
作者
Kim, Won-Chan [2 ,3 ,4 ]
Ko, Jae-Heung [1 ,5 ]
Han, Kyung-Hwan [2 ,3 ,4 ,6 ]
机构
[1] Kyung Hee Univ, Dept Plant & Environm New Resources, Yongin, South Korea
[2] Michigan State Univ, Dept Hort, E Lansing, MI 48824 USA
[3] Michigan State Univ, Dept Forestry, E Lansing, MI 48824 USA
[4] Michigan State Univ, DOE Great Lakes Bioenergy Res Ctr, E Lansing, MI 48824 USA
[5] Kyung Hee Univ, Bioenergy Ctr, Yongin, South Korea
[6] Chonnam Natl Univ, Dept Bioenergy Sci & Technol, Kwangju 500757, South Korea
基金
新加坡国家研究基金会;
关键词
cis-acting motif; MYB46; Secondary wall biosynthesis; Transcription factor; ARABIDOPSIS; EXPRESSION; GENES; GENOME; DEPOSITION; PROTEINS; SYSTEM; FAMILY; MAIZE; XYLEM;
D O I
10.1007/s11103-012-9880-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
While many aspects of primary cell wall have been extensively elucidated, our current understanding of secondary wall biosynthesis is limited. Recently, transcription factor MYB46 has been identified as a master regulator of secondary wall biosynthesis in Arabidopsis thaliana. To gain better understanding of this MYB46-mediated transcriptional regulation, we analyzed the promoter region of a direct target gene, AtC3H14, of MYB46 and identified a cis-acting regulatory motif that is recognized by MYB46. This MYB46-responsive cis-regulatory element (M46RE) was further characterized and shown to have an eight-nucleotide core motif, RKTWGGTR. We used electrophoretic mobility shift assay, transient transcriptional activation assay and chromatin immunoprecipitation analysis to show that the M46RE was necessary and sufficient for MYB46-responsive transcription. Genome-wide analysis identified that the frequency of M46RE in the promoters were highly enriched among the genes upregulated by MYB46, especially in the group of genes involved in secondary wall biosynthesis.
引用
收藏
页码:489 / 501
页数:13
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