Source: UNIV OF HAWAII submitted to NRP
MOLECULAR BREEDING OF ONCIDIUMS BEYOND YELLOW
Sponsoring Institution
State Agricultural Experiment Station
Project Status
COMPLETE
Funding Source
Reporting Frequency
Annual
Accession No.
0202540
Grant No.
(N/A)
Cumulative Award Amt.
(N/A)
Proposal No.
(N/A)
Multistate No.
(N/A)
Project Start Date
Oct 1, 2004
Project End Date
Sep 30, 2007
Grant Year
(N/A)
Program Code
[(N/A)]- (N/A)
Recipient Organization
UNIV OF HAWAII
3190 MAILE WAY
HONOLULU,HI 96822
Performing Department
TROPICAL PLANT & SOIL SCIENCE
Non Technical Summary
The mainstay of the Oncidium cut flower industry is the yellow flowered sprays of Gower Ramsey and similar yellow variants. The lack of variation in flower color limits their use as a cut flower. The purpose of this project is the development of methodologies to facilitate the establishment of new colored varieties that are crucial to the growth of the U.S. Oncidium floriculture industry.
Animal Health Component
75%
Research Effort Categories
Basic
25%
Applied
75%
Developmental
(N/A)
Classification

Knowledge Area (KA)Subject of Investigation (SOI)Field of Science (FOS)Percent
20421291080100%
Goals / Objectives
The main goal of this project is to modify Oncidium flower color, creating novel new products to help the U.S. Pacific Basin orchid grower thrive in an expanding Oncidium floriculture industry. We also propose to create a more efficient regeneration system to facilitate the development of new plants while also providing a reliable tool through which to study orchid biology at the molecular level. The goals of this study will be attained through the following objectives: 1) To express desired traits to change flower color in Oncidium Gower Ramsey, and 2) To develop a reliable and improved regeneration procedure for transformed orchids. Sometimes called the Popcorn Orchid or Dancing Ladies, the mainstay of the Oncidium cut flower industry is the yellow flowered sprays of Gower Ramsey and similar yellow variants. Although these orchids have excellent growth and propagation characteristics the lack of variation in flower color limits their use as a cut flower. Hawaii's commercial orchid growers, aware of the increase in Oncidium demand, independently expressed significant interest in the development of new varieties for cut flower production. The development of innovative new varieties is one approach to help make the U.S. Pacific Basin orchid grower more competitive in the world orchid market. The current transformation and regeneration procedures of orchids are time consuming, labor intensive and have low efficiencies with very slow regeneration times. The selection of transgenic tissue is one of the main limitations in orchid transformation. This project will use Oncidium orchids to develop a more efficient method for the regeneration of transformed orchids. The development of an improved procedure will not only benefit Oncidium, but also will be applicable to other systems including transformed Dendrobium orchid regeneration.
Project Methods
Objective 1: To express desired traits to change flower color in Oncidium Gower Ramsey. This objective seeks to generate both white and red colored Oncidiums. Preliminary work has identified the yellow color in Oncidium as due to carotenoids. As white is the most desirable color, this will be tackled from two different approaches. The first approach seeks to inhibit its formation through the floral specific inhibition of phytoene synthase, a key regulatory enzyme at the beginning of the carotenoid biosynthetic pathway. The second approach seeks to introduce enzymes to modify the floral carotenoids to colorless derivatives. The formation of a red colored Oncidium will be approached by modifying the carotenoid pathway already in place in the flower using a b-carotene ketolase isolated from the red Adonis aestivalis flower that catalyzes the conversion from b-carotene and other xanthophylls carotenoids to the red/orange colored astaxanthin. Amplified genes of interest will be cloned into plasmids containing the Arabidopsis ubiquitin-3 promoter or a floral specific promoter that we have license to use. These constructs will be co-transformed with a selection plasmid containing the nptII gene into Oncidium plbs by bombardment. After recovery transformants will be selected on media containing Geneticin. After selection the surviving plant material will be transferred to standard growth media. Once the transgenic plantlets reach a suitable size to sample leaf material plants will be analyzed by Northern analysis and HPLC carotenoid analysis. Objective 2: To develop a reliable and improved regeneration procedure for transformed orchids. We have demonstrated the ability of Oncidium plbs to be transformed and of etiolated internodes to regenerate. These procedures need to be optimized to become more efficient, reliable and faster. To achieve this we propose to extend the current regeneration and kill curve studies to test different media with various levels of hormones as well as coconut water and banana powder. The use of coconut water and banana will be investigated to enhance the formation of multiple shoots. These supplements are recognized to promote proliferation in other sympodial orchids. Once established, this work will then be extended to transformation experiments using Agrobacterium, which is known to have faster regeneration rates. Trial transformations will use the ketolase gene under control of the UBQ3 promoter, as outlined in Objective 1. The HindIII - EcoRI fragment from the plasmid encompassing the UBQ3 promoter followed by ketolase gene and a NOS terminator, will be subcloned into the HindIII - EcoRI sites of the binary vector pBINPLUS using the bordering HindIII and EcoRI sites for Agrobacterium transformation.

Progress 10/01/04 to 09/30/07

Outputs
OUTPUTS: The goal of this project to modify Oncidium flower color thereby developing novel products to help the U.S. Pacific Basin orchid grower thrive in the expanding Oncidium floriculture industry. Objective 1. To express desired traits to change flower color in Oncidium Gower Ramsey. The yellow coloration of cut flower Oncidium is due to the presence of carotenoids. We have isolated a number of carotenoid biosynthesis genes or gene fragments including, the phytoene synthase, phytoene desaturase, carotenoid isomerase and 9-cis epoxycarotenoid dioxygenase from Oncidium. Also isolated was the anthocyanin biosynthesis gene, dihydroflavonol 4-reductase, responsible for the red splotches seen in the petals, sepals and lip crest. Interestingly northern analysis has demonstrated that not all genes were up-regulated in Oncidium flowers. Some of the genes isolated demonstrated multiple copies with variations caused by insertions or deletions. Suspecting that this is due to genetic instability arising from the polyploid nature of the Oncidium Gower Ramsey cross, we have begun isolating the same genes from candidate parental plants. Although we have now isolated a number of these genes from the parental species, Oncidium sphacelatum, Oncidium flexuosum and Oncidium varicosum, we were unable to find an exact match with the genes from Oncidium Gower Ramsey. The observed minor differences are most likely due to geographic differences in source of species plants used. Objective 2. To develop a reliable and improved regeneration procedure for transformed orchids. Transformation experiments have been using both biolistic bombardment and Agrobacterium inoculation. Experiments had indicated that protocorm-like bodies (plbs) are sensitive to bombardment conditions causing sensitivity to antibiotic selection and an increased death. We have found that biolistic bombardment at lower pressures, with multiple shootings, followed by a longer recovery period better prepared the plant material for selection. Previous experiments with Agrobacterium infection of etiolated internodes demonstrated successful transient expression beta-glucuronidase expression however, regeneration from these treated tissues still remains problematic. A similar approach, as used in biolistic bombardment, to let the etiolated internodes recover after treatment while on an Agrobacterium-specific antibiotic was also unsuccessful at achieving regeneration. The current focus is on generating more plant material to continue with biolistic bombardment and regeneration experiments. TARGET AUDIENCES: Target audiences were individual oncidium orchid growers; orchid growers in Hawaii and the Hawaiian flower industry in general. Over the course of this project, results were shared at Hawaii flower grower conferences as well as national industry meetings.

Impacts
Oncidium orchids are a growing segment of orchid production in the US. Agricultural statistics in Hawaii show a steady increase in Oncidium cut-flower production and a booming up-and-coming market for potted Oncidium plants. The increase in potted plants is in part due to the excellent growth and propagation characteristics of Oncidiums. Although the cut-flower Oncidiums share these same growth characteristics, their lack of variation in flower color limits their marketability and use. The mainstay of the Oncidium cut flower industry is the yellow flowered sprays of Oncidium Gower Ramsey and similar yellow variants. This project has defined the yellow floral color compounds and also the molecular basis behind them. This data is particular useful in further developing technologies to modify the flower color in Oncidium. The successful development of innovative new varieties is crucial to the overall growth of the U.S. Oncidium floriculture industry. New varieties will directly benefit the U.S. Pacific Basin orchid grower by making them more competitive in the world orchid market.

Publications

  • Hieber, A.D., Mudalige-Jayawickrama, R.G., Kuehnle, A.R. 2006. Color genes in the orchid Oncidium Gower Ramsey: identification, expression, and potential genetic instability in an interspecific cross. Planta 223: 521-531
  • Obsuwan, K., Hieber, A.D., Mudalige-Jayawickrama R.G., Kuehnle, A.R. 2006. Functional characterization of Dendrobium and Oncidium Dfr in Petunia hybrida model. 27th International Horticulture Congress, Seoul, Korea (P335-336).
  • Mudalige-Jayawickrama, R.G., Kuehnle, A.R., Champagne, M.M., Hieber, A.D. 2006. Elucidating orchid flower colour and gene regulation of pigmentation and morphology. 4th International Workshop on Anthocyanins, Rotorua New Zealand (P39).
  • Hieber, A.D., Kuehnle, A.R., Mudalige-Jayawickrama, R.G. 2005. GenBank Accession Numbers AY953937-AY953939. Color genes in the orchid Oncidium Gower Ramsey:Dihydroflavonol 4-reductase
  • Hieber, A.D., Kuehnle, A.R. Mudalige-Jayawickrama, R.G. 2005. GenBank Accession Number AY973631. Color genes in the orchid Oncidium Gower Ramsey:Phytoene synthase
  • Hieber, A.D., Kuehnle, A.R., Mudalige-Jayawickrama, R.G. 2005. GenBank Accession Number AY973632. Color genes in the orchid Oncidium Gower Ramsey:Phytoene desaturase
  • Hieber, A.D., Kuehnle, A.R., Mudalige-Jayawickrama, R.G. 2005. GenBank Accession Numbers AY973633- AY973634. Color genes in the orchid Oncidium Gower Ramsey:Carotenoid isomerase
  • Hieber, A.D., Kuehnle, A.R., Mudalige-Jayawickrama, R.G. 2005. GenBank Accession Numbers AY974325-AY974327. Color genes in the orchid Oncidium Gower Ramsey:9-cis Epoxycarotenoid dioxygenase


Progress 10/01/05 to 09/30/06

Outputs
Transformation experiments using both biolistic bombardment and Agrobacterium inoculation have produced green tissues in the presence of selective agents. Experiment S23 of direct gene transfer using bombardments into protocorm-like bodies of Oncidium Gower Ramsey, using a ketolase gene, has produced 11 green callus tissues on 10 mg/L hygromycin. This is an improvement over an earlier experiment of protocorm-like bodies of Oncidium Gower Ramsey treated with a capsanthin synthase gene, also on 10 mg/L hygromycin selection, which resulted in no survival of green tissue. Experiment A25 using Agrobacterium infection of etiolated internodes produced 10 green shoots of Oncidium Millenium Gold and 2 green shoots of of Oncidium Gower Ramsey on 30 mg/L geneticin. Regeneration from these treated tissues thus no longer appears problematic. Additional treatments using three strains of Agrobacterium and various virulence induction protocols with liquid-grown protocorm-like bodies are in progress and tissues will be cultured on geneticin.

Impacts
Progress was made in genetic engineering of Oncidium to modify existing yellow flower color to a unique red in an effort to develop novel products to help the U.S. Pacific Basin orchid grower thrive in the expanding Oncidium floriculture industry.

Publications

  • No publications reported this period


Progress 10/01/04 to 09/30/05

Outputs
This projects goal is to modify Oncidium flower color creating novel products to help the U.S. Pacific Basin orchid grower in the expanding Oncidium floriculture industry. Objective 1. To express desired traits to change flower color in Oncidium Gower Ramsey. Previously we had isolated the phytoene synthase (PSY) gene from Oncidium. Northern analysis has since demonstrated that this gene was not up-regulated in Oncidium flowers. This result was unexpected as it is up-regulated in a number of other flower models. To find a gene that is up-regulated for future promoter studies we isolated a number of other candidate genes. Other genes or gene fragments isolated include the carotenoid biosynthesis genes, phytoene desaturase (oPDS), carotenoid isomerase (ocrtISO) and 9-cis epoxycarotenoid dioxygenase (NCED). Also isolated was the anthocyanin biosynthesis gene, dihydroflavonol 4-reductase (DFR). Northern analyses demonstrated that some of these genes were up-regulated in the floral tissue and as such are suitable for further promoter studies. Interestingly the isolation of these genes revealed in some cases multigene families with various insertions and deletions among the different members. We have hypothesized that this may be due to genetic instability arising from the polyploid nature of the Oncidium Gower Ramsey cross. This current research has culminated in a scientific paper that has recently been published in the journal Planta (Hieber et al. 2005). This work was presented to the Big Island Dendrobium Growers Association (BIDGA) in Fall 2005. Objective 2. To develop a reliable and improved regeneration procedure for transformed orchids. Previous experiments indicate that Oncidium protocorm-like bodies (plbs) are compromised by the biolistic pressure, causing sensitivity to antibiotic selection and an increase in wounding and death from certain pressures. To this end, experiments aimed at developing an Agrobacterium-based system have also been pursued. We have been able to show Agrobacterium infection of etiolated internodes and plbs by following the transient expression of the beta-glucuronidase (GUS) expression. Although regeneration has been shown for untreated etiolated internodes, experiments attempting regeneration from the treated etiolated internodes are still ongoing. Similar regeneration experiments with antibiotic selection are currently planned for the plbs.

Impacts
Oncidium orchids are an important part of floriculture production to the US orchid grower. Hawaii agricultural statistics show that the value of cut-flower Oncidium sales has been steadily increasing across the last twelve years. Although cut flower Oncidium plants have excellent growth and propagation characteristics, the lack of variation in flower color limits their marketability and use as a cut flower. New colors would greatly benefit the U.S. orchid grower. This project is presently uncovering the molecular basis behind flower color in Oncidium and is in the process of developing technologies that are directly applicable to modifying the flower color in Oncidium. These technologies are of great value to the plant geneticist to be able to research orchid cut flower's biology and to facilitate production of even better varieties. The development of novel new colors is crucial to the U.S. Pacific Basin Oncidium grower to be competitive in the world orchid market.

Publications

  • Hieber, A.D., Mudalige-Jayawickrama, R.G. and Kuehnle A.R. 2005. Color genes in the orchid Oncidium Gower Ramsey: identification, expression, and potential genetic instability in an interspecific cross. Planta. Sep 6:1-11 [Epub]