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Plant and Cell Physiology Advance Access originally published online on October 6, 2009
Plant and Cell Physiology 2009 50(11):1950-1964; doi:10.1093/pcp/pcp139
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© The Author 2009. Published by Oxford University Press on behalf of Japanese Society of Plant Physiologists. All rights reserved. For permissions, please email: journals.permissions@oxfordjournals.org

MYB83 Is a Direct Target of SND1 and Acts Redundantly with MYB46 in the Regulation of Secondary Cell Wall Biosynthesis in Arabidopsis

Ryan L. McCarthy, Ruiqin Zhong and Zheng-Hua Ye*

Department of Plant Biology, University of Georgia, 2502 Miller Plant Sciences, Athens, GA 30602, USA

*Corresponding author: E-mail, zhye{at}plantbio.uga.edu; Fax, +1-706-542-1805.


   Abstract

It has been proposed that the transcriptional regulation of secondary wall biosynthesis in Arabidopsis is controlled by a transcriptional network mediated by SND1 and its close homologs. Uncovering all the transcription factors and deciphering their interrelationships in the network are essential for our understanding of the molecular mechanisms underlying the transcriptional regulation of biosynthesis of secondary walls, the major constituent of wood and fibers. Here, we present functional evidence that the MYB83 transcription factor is another molecular switch in the SND1-mediated transcriptional network regulating secondary wall biosynthesis. MYB83 is specifically expressed in fibers and vessels where secondary wall thickening occurs. Its expression is directly activated by SND1 and its close homologs, including NST1, NST2, VND6 and VND7, indicating that MYB83 is their direct target. MYB83 overexpression is able to activate a number of the biosynthetic genes of cellulose, xylan and lignin and concomitantly induce ectopic secondary wall deposition. In addition, its overexpression upregulates the expression of several transcription factors involved in regulation of secondary wall biosynthesis. Dominant repression of MYB83 functions or simultaneous RNAi inhibition of MYB83 and MYB46 results in a reduction in secondary wall thickening in fibers and vessels and a deformation of vessels. Furthermore, double T-DNA knockout mutations of MYB83 and MYB46 cause a lack of secondary walls in vessels and an arrest in plant growth. Together, these results demonstrate that MYB83 and MYB46, both of which are SND1 direct targets, function redundantly in the transcriptional regulatory cascade leading to secondary wall formation in fibers and vessels.

Keywords: Arabidopsis - Secondary wall - Transcription factor - Transcriptional regulation

Abbreviations: CaMV, cauliflower mosaic virus; CFP, cyan fluorescent protein; GUS, β-glucuronidase; HER, human estrogen receptor; NST, NAC secondary wall thickening promoting factor; NOS, nopaline synthase; RNAi, RNA interference; SND, secondary wall-associated NAC domain protein; VND, vascular-related NAC domain; YFP, yellow fluorescent protein.

(Received September 8, 2009; Accepted September 28, 2009)
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