Changes In Floral Organs Research Articles

MADS-Box Subfamily Gene GmAP3 from Glycine max Regulates Early Flowering and Flower Development.

AP3 has been studied and is reported to affect structural changes in floral organs in various plants. However, the function of the soybean AP3 genes in flower development is unknown. Here, the full-length cDNA sequence of GmAP3 was obtained by RACE and it was verified that it belongs to the MADS-box subfamily by a bioinformatics analysis. The expression of GmAP3 is closely related to the expression of essential enzyme genes related to flower development. Yeast two-hybrid assays demonstrated that GmAP3 interacts with AP1 to determine the identity of flower organ development. A follow-up analysis showed that overexpression of the GmAP3 gene advanced flowering time and resulted in changes in floral organ morphology. The average flowering time of overexpressed soybean and tobacco plants was 6-8 days earlier than that of wild-type plants, and the average flowering time of gene-edited soybean and tobacco plants was 6-11 days later than that of wild-type plants. In conclusion, GmAP3 may directly or indirectly affect the flower development of soybean. The results of this study lay the foundation for further research on the biological functions of MADS transcriptional factors in soybeans.

Overexpression of RcLEC1-B, a HAP3 transcription factor of PLB from Rosa canina, increases the level of endogenous gibberellin and alters the development of cuticle and floral organs in Arabidopsis

The HAP3 subfamily gene RcLEC1-B, was isolated from protocorm-like body (PLB) of Rosa canina, encodes 213 amino acid residues. It was shown that RcLEC1-B was specifically expressed in PLB of R. canina and its subcellular localization is in the nucleus. Overexpression of RcLEC1-B in Arabidopsis resulted in a decrease in endogenous ABA level, an increase in GA, IAA and CTK contents, and an increased number of branches. RcLEC1-B promotes the formation of spontaneous embryoids, suggesting that it may be a homolog of the Arabidopsis LEC1 gene. RcLEC1-B-OE changed the number and morphology of flower organs and resulted in open carpels and exposed ovules, along with a reduced percentage of fertile fruit. This is the first observation that overexpression of a homolog of LEC1 in Arabidopsis can lead to morphological changes in floral organs, cuticle defects, and adhesions between organs; this may result from the increased level of gibberellin in the transgenic plants.

A report of infestation by phytoplasmas in Astraea (Euphorbiaceae) and its taxonomic implications in Astraea douradensis

Phytoplasmas infestations are widely documented in angiosperms, especially in ornamental species (Chaturverdi et al. 2010). Infestations by these phloem-limited plant pathogenic bacteria may induce several symptoms such as loss of floral meristem determinacy and abnormal flower development, including virescence of floral organs and phyllody, i.e., replacement of floral organs by leaf-like structures (Lee et al. 2000, Chatuverdi et al. 2010). However, symptoms may also vary according to the plant host and other factors, such as localization of phytoplasmas in host tissues (Bertaccini 2007). Some species may be infested but remain asymptomatic by seasonal dormancy and they may act as reservoirs for the further spread of the phytoplasmas, involving insect vectors (Dermastia et al. 2017). Developments in the detection methods of phytoplasmas have contribute to a better understanding of these intriguing bacteria, and nowadays identification of these organisms rely mostly in molecular methods such as polymerase chain reaction of selected phytoplasma-specific gene regions (Dermastia et al. 2017). Our current understanding about phytoplasmas includes knowledge on how the phenotypes linked to the infestation by phytoplasmas are triggered: Kitazawa et al. (2017) presented results which suggest that these changes in floral organs are caused by the interactions of phyllogen (a virulence factor conserved in phytoplasmas) with ABCE-class MADS domains transcription factor (MTFs), which is known as key regulator of floral organs development in angiosperms.

Overexpression of RcFUSCA3, a B3 transcription factor from the PLB in Rosa canina, activates starch accumulation and induces male sterility in Arabidopsis

A homologue of the Arabidopsis gene FUSCA3 (FUS3), isolated from the protocorm-like body (PLB) of Rosa canina and designated RcFUS3, encodes 331 amino acid residues. It was shown that RcFUS3 is specifically expressed in the PLB of R. canina and that its subcellular localization is in the nucleus. The Arabidopsis fus3-3 mutant phenotype could be rescued by over-expression of RcFUS3, suggesting that RcFUS3 has a function similar to that of Arabidopsis FUS3. Over-expression of RcFUS3 in wild type Arabidopsis resulted in a decrease in endogenous GA and CTK levels, an increase in ABA and IAA contents, starch grain accumulation in the cotyledon and hypocotyl, failure of cotyledon extension and abnormal elongation of the hypocotyl, abnormal stomatal and pavement cells, an increase in branch numbers, prolongation of the growth cycle, and morphological changes in floral organs. Interestingly, over-expression of RcFUS3 in homozygous form resulted in premature degradation of the tapetum, indehiscent anthers and hypogenetic stamens, causing complete male sterility in Arabidopsis; this is the first observation that over-expression of a gene (RcFUS3) homologous to FUS3 can lead to male sterility and starch grain accumulation in Arabidopsis.

A de novo floral transcriptome reveals clues into Phalaenopsis orchid flower development.

Phalaenopsis has a zygomorphic floral structure, including three outer tepals, two lateral inner tepals and a highly modified inner median tepal called labellum or lip; however, the regulation of its organ development remains unelucidated. We generated RNA-seq reads with the Illumina platform for floral organs of the Phalaenopsis wild-type and peloric mutant with a lip-like petal. A total of 43,552 contigs were obtained after de novo assembly. We used differentially expressed gene profiling to compare the transcriptional changes in floral organs for both the wild-type and peloric mutant. Pair-wise comparison of sepals, petals and labellum between peloric mutant and its wild-type revealed 1,838, 758 and 1,147 contigs, respectively, with significant differential expression. PhAGL6a (CUFF.17763), PhAGL6b (CUFF.17763.1), PhMADS1 (CUFF.36625.1), PhMADS4 (CUFF.25909) and PhMADS5 (CUFF.39479.1) were significantly upregulated in the lip-like petal of the peloric mutant. We used real-time PCR analysis of lip-like petals, lip-like sepals and the big lip of peloric mutants to confirm the five genes’ expression patterns. PhAGL6a, PhAGL6b and PhMADS4 were strongly expressed in the labellum and significantly upregulated in lip-like petals and lip-like sepals of peloric-mutant flowers. In addition, PhAGL6b was significantly downregulated in the labellum of the big lip mutant, with no change in expression of PhAGL6a. We provide a comprehensive transcript profile and functional analysis of Phalaenopsis floral organs. PhAGL6a PhAGL6b, and PhMADS4 might play crucial roles in the development of the labellum in Phalaenopsis. Our study provides new insights into how the orchid labellum differs and why the petal or sepal converts to a labellum in Phalaenopsis floral mutants.

Intercellular transport of epidermis-expressed MADS domain transcription factors and their effect on plant morphology and floral transition

During the lifetime of an angiosperm plant various important processes such as floral transition, specification of floral organ identity and floral determinacy, are controlled by members of the MADS domain transcription factor family. To investigate the possible non-cell-autonomous function of MADS domain proteins, we expressed GFP-tagged clones of AGAMOUS (AG), APETALA3 (AP3), PISTILLATA (PI) and SEPALLATA3 (SEP3) under the control of the MERISTEMLAYER1 promoter in Arabidopsis thaliana plants. Morphological analyses revealed that epidermal overexpression was sufficient for homeotic changes in floral organs, but that it did not result in early flowering or terminal flower phenotypes that are associated with constitutive overexpression of these proteins. Localisations of the tagged proteins in these plants were analysed with confocal laser scanning microscopy in leaf tissue, inflorescence meristems and floral meristems. We demonstrated that only AG is able to move via secondary plasmodesmata from the epidermal cell layer to the subepidermal cell layer in the floral meristem and to a lesser extent in the inflorescence meristem. To study the homeotic effects in more detail, the capacity of trafficking AG to complement the ag mutant phenotype was compared with the capacity of the non-inwards-moving AP3 protein to complement the ap3 mutant phenotype. While epidermal expression of AG gave full complementation, AP3 appeared not to be able to drive all homeotic functions from the epidermis, perhaps reflecting the difference in mobility of these proteins.

Selection of ABC genes for candidate genes of morphological changes in hydrangea floral organs induced by phytoplasma infection

The mechanism underlying the green colouration of floral organs in phytoplasma-infected hydrangeas was studied. Elucidation of morphological changes of floral organs induced by phytoplasma infection and a comparison of the expression level of genes related to floral organ morphogenesis between phytoplasma-infected and non-infected hydrangea plants was conducted. Sixteen hydrangea ( Hydrangea spp.) cultivars were used to study structural changes in floral organs induced by Japanese Hydrangea Phyllody (JHP) phytoplasma infection. The homeotic conversion of sepals to leaves was observed in different number of florets between cultivars, and was observed in 75.8–100% of the decorative florets and 2.7–67.3% of the non-decorative florets of JHP phytoplasma-infected inflorescences. The homeotic conversion of carpels to leaves was observed in 1.2–17.9% of the decorative florets and 0.1–18.9% of the non-decorative florets of infected inflorescences. The expression levels of hydrangea orthologues of class A, B and C genes were suppressed in the infected inflorescences during the developmental stage in which no morphological differences in the internal structure of floral organs have been observed. The contribution of this suppression to homeotic conversion of sepals and carpels to leaves was suggested.