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JXB Advance Access originally published online on September 12, 2008
Journal of Experimental Botany 2008 59(13):3753-3765; doi:10.1093/jxb/ern228
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© 2008 The Author(s).
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. This paper is available online free of all access charges (see
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RESEARCH PAPER

The defective seed5 (des5) mutant: effects on barley seed development and HvDek1, HvCr4, and HvSal1 gene regulation

Lene T. Olsen, Hege H. Divon, Ronald Al, Kjetil Fosnes, Stein Erik Lid and Hilde-Gunn Opsahl-Sorteberg*

Department of Plant and Environmental Sciences, Norwegian University of Life Sciences, PO Box 5003 N-1432 Ås, Norway

* To whom correspondence should be addressed: E-mail: hildop{at}umb.no

Barley, one of the major small grain crops, is especially important in climatically demanding agricultural areas of the world, with multiple uses within food, feed, and beverage. The barley endosperm is further of special scientific interest due to its three aleurone cell layers, with the potential of bringing forward the molecular understanding of seed development and cell specification from Arabidopsis and maize. Work done in Arabidopsis and maize indicate the presence of conserved seed developmental pathways where Crinkly4 (Cr4), Defective kernel1 (Dek1), and Supernumerary aleurone layer1 (Sal1) are key players. With the use of microscopy, a comprehensive phenotypic characterization of the barley defective seed5 (des5) mutant is presented here. The analysis further extends to molecular quantification of gene expression changes in the des5 mutant by qRT-PCR. Moreover, full-length genomic sequences of the barley orthologues were generated and these were annotated as HvDek1, HvCr4, and HvSal1. The most striking results in this study are the patchy reduction in number of aleurone cells, rudimentary anticlinal aleurone cell walls, and the specific change of HvCr4 expression compared to HvDek1 and HvSal1. The data presented support the involvement of Hvdes5 in establishing aleurone cells. Finally, how these results might affect the current model of aleurone and epidermal cell identity and development is discussed with a speculation regarding a possible role of Des5 in regulating cell division/ secondary cell wall building.

Key words: Aleurone cell development, anticlinal cell wall mutation, barley endosperm, Crinkly4, Defective kernel1

Received 4 July 2008; Revised 31 July 2008 Accepted 5 August 2008


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