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THE PLANT CELL, Vol 8, Issue 12 2155-2168, Copyright © 1996 by American Society of Plant Biologists
Identification of a Meristem L1 Layer-Specific Gene in Arabidopsis That Is Expressed during Embryonic Pattern Formation and Defines a New Class of Homeobox Genes
P. Lu, R. Porat, J. A. Nadeau and S. D. O'Neill
Section of Plant Biology, Division of Biological Sciences, University of California at Davis, Davis, California 95616
Homeobox genes are master regulatory genes that specify the body plan and
control development of many eukaryotic organisms, including plants. We
isolated and characterized a cDNA designated ATML1 (for Arabidopsis
thaliana meristem L1 layer) that encodes a novel homeodomain protein. The
ATML1 protein shares high sequence homology inside and outside of the
homeodomain with both the Phalaenopsis O39 and the Arabidopsis GLABRA2
(GL2) homeodomain proteins, which together define a new class of plant
homeodomain-containing proteins, designated HD-GL2. The ATML1 gene was
first expressed in the apical cell after the first asymmetric division of
the zygote and continued to be expressed in all proembryo cells until the
eight-cell stage. In the 16-cell proembryo, the ATML1 gene showed a
distinct pattern of expression, with its mRNA becoming restricted to the
protoderm. In the torpedo stage of embryo development, ATML1 mRNA
disappeared altogether but reappeared later only in the L1 layer of the
shoot apical meristem in the mature embryo. After germination, this L1
layer-specific pattern of expression was maintained in the vegetative shoot
apical meristem, inflorescence, and floral meristems, as well as in the
young floral organ primordia. Finally, ATML1 mRNA accumulated in the
protoderm of the ovule primordia and integuments and gradually became
restricted in its expression to the endothelium surrounding the embryo sac.
We propose that ATML1 may be involved in setting up morphogenetic
boundaries of positional information necessary for controlling cell
specification and pattern formation. In addition, ATML1 provides an early
molecular marker for the establishment of both apical-basal and radial
patterns during plant embryogenesis.
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