The majority of species in the large genus Solanum (ca. 1500 species) have five-merous, radially symmetrical flowers with equal stamens. However, some Solanum species and groups are characterized by four-merous and/or zygomorphic flowers, unequal stamens and enantiostyly (styles deflected to one side of the flower). Previous workers have used flower and seed coat morphology in these unusual Sol...

Studies of floral organ development in two dicotyledonous plants, Arabidopsis thaliana and Antirrhinum majus, have shown that three sets of genes (A, B and C) can pattern sepals, petals, stamens and carpels [1] [2]. Mechanisms that define boundaries between these floral whorls are unclear, however. The Arabidopsis gene SUPERMAN (SUP), which encodes a putative transcription factor, maintains the...

The Arabidopsis floral organ identity gene APETALA3 (AP3) specifies the identity of petals and stamens in the flower. In flowers mutant for the temperature-sensitive ap3-1 allele, the petals and stamens are partially converted to sepals and carpels, respectively. ap3-1 contains a single nucleotide change in the AP3 gene that alters both an amino acid in the AP3 protein and the 5' splice consens...

BACKGROUND AND AIMS Flower morphology and inflorescence architecture affect pollinator foraging behaviour and thereby influence the process of pollination and the reproductive success of plants. This study explored possible ecological functions of the lever-like stamens and the floral design in Salvia cyclostegia. METHODS Flower construction was experimentally manipulated by removing either t...

Differential growth of tissues during lateral organ development is essential for producing variation in shape and size. Previous studies have identified JAGGED (JAG), a gene that encodes a putative C2H2 zinc-finger transcription factor, as a key regulator of shape that promotes growth in lateral organs. Although JAG expression is detected in all floral organs, loss-of-function jag alleles have ...

The ABC model of flower organ identity is widely recognized as providing a framework for understanding the specification of flower organs in diverse plant species. Recent studies in Arabidopsis thaliana have shown that three closely related MADS-box genes, SEPALLATA1 (SEP1), SEP2 and SEP3, are required to specify petals, stamens, and carpels because these organs are converted into sepals in sep...

An open question in developmental biology is how groups of dividing cells can generate specific numbers of segments or organs. We describe the phenotypic effects of mutations in PERIANTHIA, a gene specifically required for floral organ patterning in Arabidopsis thaliana. Most wild-type Arabidopsis flowers have 4 sepals, 4 petals, 6 stamens, and 2 carpels. Flowers of perianthia mutant plants mos...