Expression of floral MADS-box genes in basal angiosperms: implications for the evolution of floral regulators
Article first published online: 10 AUG 2005
The Plant Journal
Volume 43, Issue 5, pages 724–744, September 2005
How to Cite
Kim, S., Koh, J., Yoo, M.-J., Kong, H., Hu, Y., Ma, H., Soltis, P. S. and Soltis, D. E. (2005), Expression of floral MADS-box genes in basal angiosperms: implications for the evolution of floral regulators. The Plant Journal, 43: 724–744. doi: 10.1111/j.1365-313X.2005.02487.x
- Issue published online: 10 AUG 2005
- Article first published online: 10 AUG 2005
- Received 16 February 2005; revised 5 June 2005; accepted 10 June 2005.
- basal angiosperms;
- plant evolution;
- relative-quantitative RT-PCR;
- in situ hybridization
The ABC model of floral organ identity is based on studies of Arabidopsis and Antirrhinum, both of which are highly derived eudicots. Most of the genes required for the ABC functions in Arabidopsis and Antirrhinum are members of the MADS-box gene family, and their orthologs are present in all major angiosperm lineages. Although the eudicots comprise 75% of all angiosperms, most of the diversity in arrangement and number of floral parts is actually found among basal angiosperm lineages, for which little is known about the genes that control floral development. To investigate the conservation and divergence of expression patterns of floral MADS-box genes in basal angiosperms relative to eudicot model systems, we isolated several floral MADS-box genes and examined their expression patterns in representative species, including Amborella (Amborellaceae), Nuphar (Nymphaeaceae) and Illicium (Austrobaileyales), the successive sister groups to all other extant angiosperms, plus Magnolia and Asimina, members of the large magnoliid clade. Our results from multiple methods (relative-quantitative RT-PCR, real-time PCR and RNA in situ hybridization) revealed that expression patterns of floral MADS-box genes in basal angiosperms are broader than those of their counterparts in eudicots and monocots. In particular, (i) AP1 homologs are generally expressed in all floral organs and leaves, (ii) AP3/PI homologs are generally expressed in all floral organs and (iii) AG homologs are expressed in stamens and carpels of most basal angiosperms, in agreement with the expectations of the ABC model; however, an AG homolog is also expressed in the tepals of Illicium. The broader range of strong expression of AP3/PI homologs is inferred to be the ancestral pattern for all angiosperms and is also consistent with the gradual morphological intergradations often observed between adjacent floral organs in basal angiosperms.