Abstract

Aristolochia fimbriata (Aristolochiaceae: Piperales) exhibits highly synorganized flowers with a single convoluted structure forming a petaloid perianth that surrounds the gynostemium, putatively formed by the congenital fusion between stamens and the upper portion of the carpels. Here we present the flower development and morphology of A. fimbriata, together with the expression of the key regulatory genes that participate in flower development, particularly those likely controlling perianth identity. A. fimbriata is a member of the magnoliids, and thus gene expression detected for all ABCE MADS-box genes in this taxon, can also help to elucidate patterns of gene expression prior the independent duplications of these genes in eudicots and monocots. Using both floral development and anatomy in combination with the isolation of MADS-box gene homologs, gene phylogenetic analyses and expression studies (both by reverse transcription PCR and in situ hybridization), we present hypotheses on floral organ identity genes involved in the formation of this bizarre flower. We found that most MADS-box genes were expressed in vegetative and reproductive tissues with the exception of AfimSEP2, AfimAGL6, and AfimSTK transcripts that are only found in flowers and capsules but are not detected in leaves. Two genes show ubiquitous expression; AfimFUL that is found in all floral organs at all developmental stages as well as in leaves and capsules, and AfimAG that has low expression in leaves and is found in all floral organs at all stages with a considerable reduction of expression in the limb of anthetic flowers. Our results indicate that expression of AfimFUL is indicative of pleiotropic roles and not of a perianth identity specific function. On the other hand, expression of B-class genes, AfimAP3 and AfimPI, suggests their conserved role in stamen identity and corroborates that the perianth is sepal and not petal-derived. Our data also postulates an AGL6 ortholog as a candidate gene for sepal identity in the Aristolochiaceae and provides testable hypothesis for a modified ABCE model in synorganized magnoliid flowers.

Highlights

  • With approximately 550 species, Aristolochia is the largest genus in the Aristolochiaceae, one of the families of the monophyletic order Piperales (APG, 2009)

  • At stage 2 (S2) the individual sepal primordia become fused in a dome-shaped perianth, which begins to undergo asymmetric intercalary growth, as the abaxial region corresponding to the median sepal grows noticeably faster (Figures 2E,F)

  • By Stage 5 (S5), the future abscission zone between the perianth and the inferior ovary is formed, and a proper utricle, tube and limb can be distinguished (Figure 2I); simultaneously, the six stigmatic lobes gradually elongate fused to the inner side of the anthers, overtopping them, forming the gynostemium (Figures 3E–H)

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Summary

Introduction

With approximately 550 species, Aristolochia is the largest genus in the Aristolochiaceae, one of the families of the monophyletic order Piperales (APG, 2009). Flowers in the genus differ from those of the other members of the family (Asarum L., Thottea Rottb., Lactoris Phil., Hydnora Thunb., and Saruma Oliver) in that its perianth is monosymmetric, and formed by a trimerous whorl of petaloid sepals fused to form a variously convoluted and tubular structure, differentiated in three regions: a basal, inflated portion called the utricle; a narrow, tubular portion called the tube; and an expanded, laminar portion called the limb (Figure 1). Ontogenetic studies have shown that the gynostemium is formed by the congenital fusion of stamens and stigmas (González and Stevenson, 2000a,b). This suite of floral characters is unique among early diverging flowering plants, and strongly differ from the predominant floral construction among magnoliids based on a large number of spirally arranged organs and a predominantly apocarpic and superior ovary (Endress and Doyle, 2007). The floral construction in Aristolochia poses a number of questions regarding the origin, development, and genetic identity of whorls in early diverging synorganized flowers

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