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Published March 1991 | Published
Journal Article Open

AGL1-AGL6, an Arabidopsis gene family with similarity to floral homeotic and transcription factor genes

Abstract

The predicted products of floral homeotic genes, AGAMOUS (AG) from Arabidopsis thaliana and DEFICIENS A (DEF A) from Antirrhinum majus, have been shown previously to share strong sequence similarity with transcription factors from humans (SRF) and yeast (MCM1). The conserved sequence between these proteins is localized within a domain known to be necessary for the DNA binding and for the dimerization of SRF. We have isolated six new genes from A. thaliana, AGL1-AGL6, which also have this conserved sequence motif. On the basis of the sequence comparison between the AG and AGL genes, they can be assigned to two subfamilies of a large gene family. RNA dot blot analysis indicates that five of these genes (AGL1, AGL2, AGL4, AGL5, and AGL6) are preferentially expressed in flowers. In addition, in situ RNA hybridization experiments with AGL1 and AGL2 show that their mRNAs are detected in some floral organs but not in others. Our results suggest that these genes may act to control many steps of Arabidopsis floral morphogenesis. In contrast, the AGL3 gene is expressed in vegetative tissues as well as in flowers, suggesting that it functions in a broader range of tissues. We discuss possible roles of this gene family during the evolution of flowers.

Additional Information

© 1991 Cold Spring Harbor Laboratory Press. The Authors acknowledge that six months after the full-issue publication date, the Article will be distributed under a Creative Commons CC-BY-NC License (Attribution-NonCommercial 4.0 International License, http://creativecommons.org/licenses/by-nc/4.0/). Received October 30, 1990; revised version accepted December 28, 1990. We thank S. Kempin for help with RFLP mapping, L. Medrano for excellent technical assistance, G. Drews and I. Bowman for advice on the in situ hybridization experiments, D. Spector and L. Fields for help with photography of in situ slides, A. Tagle for assistance in preparation of this manuscript, and I. Bowman, L. Brockman, C. Chang, G. Drews, B. Hamilton, T. lack, L. Sieburth, V. Sundaresan, A. van der Bliek, and D.Weigel for valuable comments on this manuscript. This work was supported by grants from the National Science Foundation (DCB 8703439) and the Lucille P. Markey Charitable Trust. H.M. was supported by a postdoctoral fellowship from the Helen Hay Whitney Foundation, and M.F.Y. was supported by a postdoctoral fellowship in plant biology from the National Science Foundation {DCB 8608456).The sequence data described in this paper have been submitted to the GenBank database, and the accession numbers are AGL1, M55550; AGL2, M55551; AGL4, M55552; AGLS, M55553; and AGL6, M55554. The publication costs of this article were defrayed in part by payment of page charges. This article must therefore be hereby marked "advertisement" in accordance with 18 USC section 1734 solely to indicate this fact.

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August 22, 2023
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