Regulation of Flowering Timing by ABA-NnSnRK1 Signaling Pathway in Lotus

The lotus produces flower buds at each node, yet most of them are aborted because of unfavorable environmental changes and the mechanism remains unclear. In this work, we proposed a potential novel pathway for ABA-mediated flower timing control in the lotus, which was explored by combining molecular, genetic, transcriptomic, biochemical, and pharmacologic approaches. We found that the aborting flower buds experienced extensive programmed cell death (PCD). The hormonal changes between the normal and aborting flower buds were dominated by abscisic acid (ABA). Seedlings treated with increasing concentrations of ABA exhibited a differential alleviating effect on flower bud abortion, with a maximal response at 80 μM. Transcriptome analysis further confirmed the changes of ABA content and the occurrence of PCD, and indicated the importance of PCD-related SNF1-related protein kinase 1 (NnSnRK1). The NnSnRK1-silenced lotus seedlings showed stronger flowering ability, with their flower:leaf ratio increased by 40%. When seedlings were treated with ABA, the expression level and protein kinase activity of NnSnRK1 significantly decreased. The phenotype of NnSnRK1-silenced seedlings could also be enhanced by ABA treatment and reversed by tungstate treatment. These results suggested that the decline of ABA content in lotus flower buds released its repression of NnSnRK1, which then initiated flower bud abortion.

Molecular characterization and expression patterns of PsSVP genes reveal distinct roles in flower bud abortion and flowering in tree peony (Paeonia suffruticosa)

Wang, S., Xue, J., Ahmadi, N., Holloway, P., Zhu, F., Ren, X. and Zhang, X. 2014. Molecular characterization and expression patterns of PsSVP genes reveal distinct roles in flower bud abortion and flowering in tree peony (Paeonia suffruticosa). Can. J. Plant Sci. 94: 1181–1193. Container culture and flower forcing are used for off-season production of tree peony for the Chinese Spring Festival. Storage of potted tree peony for 10 d at 12°C in a refrigerator before 4°C chilling treatment can help new root growth and promote leaf development. Development from bud swelling to anthesis was divided into nine stages. Some aborted flower buds usually emerge in Stage III. Removal of two to four leaflets in an alternating pattern and applying gibberellic acid 3 (GA3) around the flower bud at Stage III can decrease the flower bud abortion rate and promote flower formation rate. Two MADS-box genes with homology to Arabidopsis SVP, designated PsSVP1 and PsSVP2, which probably caused flower-bud abortion, were isolated by reverse transcription-PCR. Sequence comparison analysis showed that PsSVP was most similar to SVP-like gene in apple. Phylogenetic analysis indicates that PsSVP was evolutionarily close to SVP-like genes from Malus domestica, SVP genes from Cruciferae and SVP-like genes from Vitis vinifera. The qRT-PCR results suggested that expression of PsSVP was high in vegetative growth phase, especially in the leaves of tree peony, and its expression was regulated by GA3. Further analysis showed that more PsSVP transcripted in the aborted flower bud, especially in the buds where leaflets grew well. It was deduced that PsSVP can promote vegetative growth and suppress flowering in tree peony. Thus, it is very important to further investigate PsSVP and decipher the mechanisms of flower-bud abortion to improve forcing culture of tree peony.

Residual Effects of Ethylene on Tulip Growth and Flowering

Ethylene effects were investigated on two tulip (Tulipa gesneriana L.) cultivars, Markant and Carreria. Pre-cooled bulbs were treated with ethylene (flow-through) for 1 week at 0, 0.1, 1.0, or 10 μL·L−1 (± 10%) in a modified hydroponic system. After ethylene exposure, plants were either destructively harvested for root measurements or forced in a greenhouse for flower measurements. Ethylene exposure at concentrations as low as 1 μL·L−1 during the first week of growth reduced shoot and root elongation and subsequently increased flower bud abortion. At 10 μL·L−1, root growth was essentially eliminated. In a second experiment, bulbs were treated overnight with 1-methylcyclopropene (1-MCP) before a 7-day exposure to 1 μL·L−1 ethylene. 1-MCP pretreatment eliminated the harmful effects of ethylene on root and shoot growth. This study illustrates the effects of ethylene exposure during hydroponic tulip production and demonstrates a potential benefit to treating bulbs with 1-MCP before planting.

Salinity and Growing Medium Regulate Growth, Morphology and Ion Uptake of Gaillardia aristata

A study was conducted to characterize the response of Gaillardia aristata Pursh to salinity (0.8, 2.0 or 4.0 dS/m) and growing media: 100% perlite (Perlite), 100% Sunshine Mix No. 4 (Mix), 1 to 1 (by vol) perlite and Sunshine Mix No. 4 (Perlite Mix), or 1 to 1 Sunshine Mix No. 4 and composted mulch (Mix Mulch). Type of medium did not influence shoot dry weight (DW). However, root to shoot DW ratio was highest for plants grown in Perlite. Shoot DW of plants irrigated with tap water (0.8 dS/m) was higher compared to those irrigated with saline solution at 2.0 or 4.0 dS/m, except for those grown in Mix. Salinity did not alter the root to shoot DW ratio. In general, elevated salinity led to relatively short plants. Plants were taller when grown in Perlite or Mix Mulch with fewer lateral shoots compared to plants grown in Mix and Perlite Mix. Flower bud abortion occurred in plants grown in Mix or Perlite Mix, while this phenomenon was not observed in plants grown in Perlite or Mix Mulch. Overall, plants performed better in Perlite and Mix Mulch than Mix and Perlite Mix.

ETHYLENE IN STORAGE: AN EVALUATION OF THREE INFLUENTIAL FACTORS ON TULIP BULBS' SENSITIVITY TO ETHYLENE DURING POSTHARVEST SHIPPING AND STORAGE

During transport and the subsequent storage of tulip bulbs, inadvertent failure in ventilation and/or high contamination of Fusarium-infected bulbs may expose healthy bulbs to high concentrations of ethylene. Ethylene is known to cause many detrimental effects on forcing quality, including gummosis, increased respiration, flower bud abortion, bulb splitting and poor rooting. In this work, exposure duration and timing as well as the post-stress storage temperatures were evaluated for their potential effects on ethylene sensitivity in bulbs of four tulip cultivars. Degree of damage in sensitive cultivars `Apeldoorn' and `World's Favourite' increased with days at about 10 ppm ethylene starting at 9 and 16 days respectively. This effect strongly depended on timing of ethylene stress, as late treated bulbs showed more severe responses to ethylene treatment than early treated bulbs. Additionally, bulbs that were cooled immediately after ethylene stress, compared with those stored at 17 °C after stress, have significantly higher flowering quality in all attributes measured. This response was also strongly dependent on timing of ethylene stress and cultivar. Implications of the potential cold reversal of ethylene damage as well as effects of ethylene exposure duration and timing of stress on shipping and storage recommendations will be discussed.