- Open Access
MicroRNA, sex determination and floral meristem determinacy in maize
© BioMed Central Ltd 2008
Published: 30 January 2008
Sex determination in the flowers of maize involves the abortion of stamen or pistil development. Recent work investigating genes that control this process reveals that a microRNA is involved in both the sex determination of the male inflorescence and its growth pattern.
The decision to develop as a male or female is fundamental to most life forms. In animals the genetic and environmental signals that influence this decision are diverse and the subject of intense study, yet this question has received relatively little attention in plants. Why the difference? While unisexuality is common in animals, it is not so common in flowering plants. The model plant Arabidopsis thaliana, for example, has perfect (bisexual) flowers with pollen-producing stamens and ovule-producing pistils wrapped in whorls of petals and sepals. While we have a clear understanding of how the identity of floral organs is controlled in Arabidopsis, this plant is of limited value for understanding how plant species have attained unisexuality. For the most part, flowering plants with bisexual flowers have collectively evolved a multitude of additional and interesting mechanisms to avoid self-fertilization, which most animal species avoid by making sure that each individual is unisexual and populations have equal proportions of males and females.
Of those flowering plant species that do produce unisexual flowers, some are dioecious, having strictly male or female flowers and unisexual individuals, whereas others are monoecious and produce both unisexual male and female flowers but on the same plant. Maize (Zea mays) is a monoecious plant that produces imperfect (unisexual) male flowers, or florets, in the tassel and imperfect female florets in the ear. In maize, imperfect florets arise by the arrest of stamen development in female flowers and by the abortion of pistil primordials in the male, suggesting that sex determination is not a problem of floral-organ identity, but rather a matter of what regulates the arrest of stamen or pistil development in the ear and tassel florets, respectively. In maize, the application of the plant hormone gibberellin (GA) to tassels feminizes the tassel, whereas depletion of endogenous GA masculinizes ear florets , indicating that stamen and pistil development are under hormonal control. Given the rich history of maize genetics and the agronomic importance of its seeds, maize is an excellent and important system for understanding how unisexuality can evolve in flowering plants.
The architecture of the maize tassel is fairly complex (Figure 1a), even though the hundreds of individual tassel florets are extremely reduced in size and simple in structure, as illustrated in Figure 1b. Each male floret consists of two bracts (the lemma and palea), two minute scales called lodicules, and three stamens. Florets are organized into units, called spikelets, with each spikelet enclosed by two bracts called glumes. In maize, each male spikelet contains two florets, while those in the ear contain one. The spikelets are collectively organized into units called spikes, with many spikes collectively making up the tassel. The organization of spike, spikelets and florets is engineered by the inflorescence apical meristem, which contains the population of stem cells that deliver new daughter cells to the growing plant. As the spike inflorescence develops, the inflorescence meristem continuously forms new branch derivatives that initiate spikelet pair meristems; after branching, each spikelet pair meristem undergoes a transition to produce two spikelet meristems; each spikelet meristem then undergoes a transition to produce two floret meristems that initiate the organs of the floret. Eventually, all meristems terminate, the florets mature, open and shed their pollen.
The tassels of mutant ts4 plants differ from wild type in several ways (see Figure 1a): they have feminized florets, show increased spikelet branching and typically produce more than two florets per spikelet. The increase in branching and floret number reflects an inability of the meristems to switch from an indeterminate to a determinate state as the tassel develops. Thus, in addition to promoting male development, the wild-type ts4 gene functions to impose determinacy on the spikelet and spikelet pair meristems.
To understand how these tasselseed genes control sex determination in the male floret, Chuck and colleagues  cloned the ts4 gene and discovered that it is a member of the miR172 family of microRNAs (miRNAs) that is known to regulate the APETALA2 (AP2) family of transcription factors [4, 5]. As it turns out, the same authors had previously shown that the maize indeterminate spikelet1 (ids1) gene encodes an AP2-like gene . Like ts4 tassels, ids1 tassels produce additional florets; however, ids1 florets in the tassel are not feminized like the ts4 florets.
How ids1 affects branching and meristem transitions is not clear, although some clues are provided by the characterization of ap2 mutations in Arabidopsis. In Arabidopsis, ectopic expression of a mutant form of ap2 altered in its miRNA172-binding site leads to several floral defects, including the loss of floral determinacy . This phenotype mimics the agamous (ag) phenotype, consistent with the function of AG as necessary for carpel initiation . Chuck et al.  propose that a similar relationship between ids1 and an AG-like gene could occur in maize. By reducing AG expression in the floret, the prolonged expression of ids1 would prevent the differentiation of stem cells in the meristem, thus allowing the spikelet meristem to form additional floret meristems. This and other hypotheses remain to be tested.
From an evolutionary perspective, it will be interesting to see if the mechanism of sex determination in maize that is defined by ts4 and ids1 is common to other monoecious or dioecious species of plants, including the homosporous ferns, which determine their sexual phenotype during the gametophytic phase of growth and where meristem development and sex determination go hand-in-hand . Given that monoecy has evolved multiple times in different angiosperm lineages, and dioecy often follows , the study of Chuck et al.  provides new tools to understand how widespread this mechanism of sex determination is.
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