Scientists have studied the flowering of higher plants for nearly a hundred years. The flowering process is extremely complex. Many studies have shown that the floral development process in plants is controlled not only by the complex regulation of multiple genes in internal factors, but also by a variety of environmental factors [1]. In recent years, the Flowering Locus T (FT) gene has been the most widely studied and effective gene in promoting early flowering in plants [2–4]. In addition, its homologous genes PtFT1, CiFT, Hd3a, and SFT have been isolated from poplar, citrus, rice, and tomato, respectively, and the overexpression of these genes can promote early flowering in transgenic plants [5–8]. The FT gene and its homologous genes are found in a variety of plants and therefore play similarly important roles; many studies have shown the protein encoded by the FT gene may be the major component of the “flowering hormone” [9,10]. In the present paper, some functions of the FT gene and research progress of the FT protein are briefly reviewed to further shed light on the function of FT genes and their products.

The first researcher to study the flowering mechanism was Julis Sachs, who proposed the concept of the flowering material in 1865 following the flowering induction experiment [11]. He used a variety of related experiments to show that the floral promoting factor was first produced in leaves then transported over a long distance through the stem to produce buds that promote flowering. Chailakhyan first proposed the concept of the flowering hormone in 1936 and named this flowering-promoting material [12]. Experimental evidence confirmed that the flowering hormone as a common element in a variety of flowering plants. Such data have greatly stimulated research interest to identify the flowering hormone, but no result has been observed. Huang et al. [13] demonstrated the flowering hormone might be associated with the FT mRNA. This finding brought the attention of many scientists to the FT gene and its products. However, Corbesier et al. [14] subsequently suggested the FT mRNA is not a flowering hormone but an intermediate product, while the real flowering hormone should be the end product FT protein. This claim was proven by two experiments. First, FT protein was confirmed to promote flowering through long-distance transport, as observed using FT protein fused to green fluorescent protein (GFP). Second, grafting experiments of Arabidopsis mutants also proved that the FT protein could be transported over long distances and could ultimately promote flowering. In the course of the experiment, FT mRNA transport was not detected, indicating that the FT protein may be the major component of the flower hormone. Under a long-day photoperiod, the FT protein of Arabidopsis moves from leaves to the top and eventually interacts with Flowering Locus D (FD). The FT-FD complex formed directly or indirectly activates the flower-type genes, such as APETALA1 (AP1) genes and ultimately promotes flowering in Arabidopsis [15,16]. The FT protein is part of the phloem transfer signal, which has been proven in the FT protein homologue in the phloem sap of rice, gourds, and Brassica [17–19]. Subsequently, a number of related studies proved that during the FT-mediated flowering process, the floral-promoting signal, which can be transferred from leaves to the apical meristem, is mainly composed of the FT protein [7,20–23].

FT expression products include FT mRNA and FT protein. In 2005, FT mRNA was considered the flowering hormone or its important component. This concept was later disproved, because previous experiments could not be repeated, and in later grafting experiments, FT protein, instead of FT mRNA, was finally detected. FT protein is a class of the CETS family, with a molecular weight of approximately 20 kDa [51]. This protein has a similar sequence and protein-folding structure to mammalian Raf Kinase Inhibitor Protein, and is homologous to the Phosphatidylethanolamine Binding Protein protein [52].

Lin et al. in 2007 [19] used Zucchini yellow mosaic virus-mediated transient expression of Arabidopsis in short-day pumpkin to illustrate the conservation of the FT protein [19]. The presence of the FT protein was also reported in rape [18]. The FT protein can be transported from the phloem to the top to induce flowering [19]. The rice FT homologue Hd3a was found in the inner region of the SAM and in stem and leaf blade vascular tissues, suggesting that it is produced in the vascular tissue of the leaf blade, transported through stem phloem tissue, unloaded at the upper end of the vascular tissue, and translocated to the SAM, probably through the region just beneath the SAM. These results suggest that the Hd3a protein, but not Hd3a mRNA, is a candidate for the florigen in rice [23]. Furthermore, Hd3a interacts with 14-3-3 proteins in the apical cells of shoots, yielding a complex that translocates to the nucleus and binds to the Oryza sativa FD1 transcription factor, a rice homologue of Arabidopsis thaliana FD. The resultant ternary “florigen activation complex” (FAC) induces transcription of OsMADS15, a homologue of AtAPETALA1 (AP1), which leads to flowering. Taoka et al. in 2011 [53] have determined the 2.4 Å crystal structure of rice FAC, which provides a mechanistic basis for florigen function in flowering. The results indicated that 14-3-3 proteins act as intracellular receptors for florigen in shoot apical cells, and offer new approaches to manipulate flowering in various crops and trees. By these successful experiments, the FT protein is seen to have the features of most flowering hormones. It is conservative and can be transported over a long distance to the apical meristem. The FT protein can be detected in repetitions of the same experiment and experiments with different materials, but the FT protein cannot be concluded to be the flowering hormone. Liu et al. in 2008 [54] used a turnip mosaic virus with deletion of Coat Protein (CP) (TCVΔCP) as the vector, cloned FT and mFT (start codon was mutated into stop codon) sequences into the location of the original CP sequence transformed into Arabidopsis, and detected their sequences in unvaccinated upper new leaves and buds to investigate whether FT mRNA has a role in transferring important signals during plant growth and development. In contrast, the GFP sequence, which was added as a control variable, was not detected in the same area. These results showed that FT and mFT sequences are able to restore the intercellular mobility of TCVΔCP.

Flower development is an important decision of higher plants and is regulated by a variety of flowering genes. The FT gene mainly affects the induction of flowering. Studies have identified its homologous genes in a variety of garden plants, fruit trees, and vegetables. Transgenic technology confirmed that the gene can promote early flowering in plants. Thus, the genetic engineering approach can be used to perform genetic reformation on the flowering genes in wood, such as ginkgo, to shorten their young period.

FT genes are conserved among different species. Although the FT gene and its expression products are somewhat understood, many issues still need to be further studied. One issue is the difference in expression and functions of FT genes between gymnosperms and angiosperms, between annual and perennial plants, and between different parts of the same plant, and how its expression is regulated. Although FT mRNA is not detected during the transfer process, whether it is unrelated to the flowering hormone is another issue to be considered. Moreover, it need to be ascertained whether the reasons that the FT protein has not been detected for a long time are its special structure or low content, the type of FT gene promoter, and how it is regulated. Likewise, more topics of concern are whether the present FT signal graft transfer is of high practical value, and what the transport mechanism and distribution pattern during FT grafting are. Answers to these questions are not clear now, and many related minor issues have also arisen. When these issues are satisfactorily resolved, the concept of the “flowering hormone” and the FT gene and its expression product will be better understood. The resolution will also be a guide to control the flowering of fruit trees, flowers, and vegetables.