U.S. patents available from 1976 to present.
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Grape plant named ‘Improved Chancellor’

Patent PP20428 Issued on October 20, 2009. Estimated Expiration Date: Icon_subject August 17, 2025. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.
Abstract Claims Description Full Text

Patent References

Microorganisms and plasmids for 2,4-dichlorophenoxyacetic acid (2,4-D) monooxygenase formation and process for the production of these plasmids and strains
Patent #: 6153401
Issued on: 11/28/2000
Inventor: Streber, et al.

Regeneration system for grape and uses thereof Patent #: 6455312
Issued on: 09/24/2002
Inventor: Gray, et al.

Inventors

Assignee

Application

No. 11206645 filed on 08/17/2005

US Classes:

PLT/205Grape

Examiners

Primary: Bell, Kent L

Attorney, Agent or Firm

International Class

A01H 5/00

Description

Genus: Vitis (complex interspecific hybrid lineage).


BACKGROUND AND SUMMARY OF THE INVENTION

The new grape plant named `Improved Chancellor` is of Vitis parentage, with the breeding chart tracing the lineage as shown in FIG. 3.

The new grapevine resulted from stably introducing a plant expressible tfdA gene from Ralstonia eutrophus into Chancellor grapes. The tdfA gene confers resistance in plants to the phenoxy herbicides, especially 2,4 D (2,4-diphenoxyacetic acid). For a general discussion, see U.S. Pat. Publication No. 2003-0154507. This resistance improves the performance of grapevines, which are by nature exquisitely sensitive to the phenoxy herbicides, with deleterious effects observed with drift ofherbicide from fields in the area, especially grain fields sprayed to control broadleaf weeds. Damage from drift negatively affects growth and/or yield in affected vineyards.

DESCRIPTION OF THE INVENTION

The transgenic 2, 4-D resistant `Chancellor` grape was produced via genetic engineering. Embryogenic callus was initiated from ovary explants dissected from flower buds 10-14 days before anthesis on Nistch and Nistch (1969) medium containing 9μM 2, 4-D, 17 μM IASP, and 1 μM BAP in darkness. Embryogenic callus was proliferated and maintained in NN medium containing 2 μM 2, 4-D, 0.2 μM TDZ and 4 μM IASP (Long Term Maintenance Medium, LTMM). Embryogenic callus cultivated for5 weeks in LTMM was infected with Agrobacterium tumefaciens strain LBA4404:pAL4404 carrying a pBIN19 plant transformation plasmid vector containing the tfdA gene construct. The 864 bp tfdA gene in the construct is driven by the CaMV35S core promoter andlinked to the nos gene terminator. Transformed embryogenic cells were selected on LTMM containing 350 mg l-1 kanamycin and induced to develop somatic embryos on NN medium supplemented with 10 μM IASP, 8 μM NOA, 1 μM TDZ, 1 μM ABA and2.5 g l-1 activated charcoal (Embryo Development and Maturation Medium, EDMM). Somatic embryos were germinated and converted into plantlets in 1/2 MS (Murashige & Skoog, 1962) medium containing 0.5 μM BA+0.025 μM NAA. PCR analysis ofregenerated plantlets with tfdA-specific primers showed they contained the tfdA gene. The expression of the tfdA gene in the transgenic plants was demonstrated by their 2, 4-D resistance during spray tests. Transgenic plants survived treatment with0.5, 5, and 10 kg ha-1 of 2-ethylhexyl ester of 2, 4-D. These rates killed non-transgenic plants.

Spray tests utilized applications of 2,4D corresponding to field application rates of 0, 0.5, 5 and 10 kg/ha of a commercial herbicide preparation (LV400, Growmark Inc). After spraying, the transgenic plant and wild type plants were allowed todry and then transferred to an isolation greenhouse, and they were observed for damage over a period of three weeks. The wild type plants showed signs of damage within two hours of spraying and they were all dead within one week. While the transgenicplant showed minor, short lived injury (leaf epinasty) for up to seven days at the 2 higher doses of 2 4-D, there was full recovery, with normal growth at the end of two weeks.

The original vine of `Improved Chancellor` arose from selection among embryogenic cells developed in vitro. The cells had been transformed with the tfdA gene. About 20 plants were regenerated between 2002 and 2003; `Improved Chancellor` wasselected from these. It was then micropropagated by cuttings in Urbana, Ill. Those resulting plants were stable and typical of the original vine. `Improved Chancellor's` resistance to 2,4-D was confirmed in 2004 in the original plant and in asexuallypropagated material from the original plant. Subsequent asexual propagations of the variety have also proven stable with true to type plants.

COMPARISON WITH PARENTAL CULTIVAR

The new grape plant named `Improved Chancellor` resembles the parent grape, from which it was produced by genetic modification, but it differs in that it is significantly less sensitive to herbicide 2,4-D. The fruit color, flavor and texture isexpected to be similar to the original grape. Vigor of the new variety is the same as the parent plant in absence of herbicide. However, vigor of `Improved Chancellor` is increased over that of the parent plant in the presence of herbicide.

DESCRIPTION OF THE FIGURES

FIG. 1 Shows canes, leaves, and tendrils of `Improved Chancellor` (left) in comparison to the parent (right)

FIG. 2 Shows fruit clusters of parental `Chancellor` at harvest.

FIG. 3 Shows the breeding chart tracing the lineage of `Improved Chancellor`.

DETAILED BOTANICAL DESCRIPTION OF THE INVENTION

The following description of grapevine contains references to color names taken from the Ridgeway Color Standards and Color Nomenclature (1912, Hoen and Co., Baltimore, Md.). Descriptors used herein conform to those set forth by theInternational Board for Plant Genetic Resources Institute Grape Descriptors (Vitis spp.) of 1983 and/or 1997 which were developed in collaboration with the Office International de la Vigne et du Vin (OIV) and the International Union for the Protection ofNew Varieties of Plants (UPOV) and published in Descriptors for Grapevine (Vitis spp.) (Anonymous, International Plant Genetic Resources Institute, 1997, ISBN 92-9043-352-3).

Descriptions of the new invention apply to vines of `Improved Chancellor` grown in an isolation greenhouse in the year 2005. These vines were in their first year of growth having been transplanted from in vitro to the greenhouse in December2004. The parent clones (control) were growing on their own roots in Urbana, Ill. The descriptions of the parent plants apply generally to the new variety grown under similar circumstances elsewhere:

VINE

General: Vigor.--Too young to give valid data. Productivity.--Unavailable. Hardiness.--Unavailable. Rootstock.--None. LEAVES Mature leaves: Average blade length 8.6 cm. Average blade width 12.5 cm. Size of blade.--Large. Shape.--Pentagonal. Anthocyanin coloration of main veins on the upper side of the blade. Present at base of veins on mature leaves, Dahlia Purple, 67.V-R.m Plate XII. Anthocyanin coloration of main veins on lower leaf surface.--Clear Yellow Green,31.Y-G. Plate VI. Mature leaf profile.--Undulating. Blistering surface of blade upper surface.--Absent. Leaf blade tip.--Curved downward. Margins.--Serrate. Apex.--Acuminate. Base.--Sagittate. Thickness.--0.06552 in. Undulation of blade betweenmain and lateral veins.--Medium. Shape of teeth.--Conical, both sides convex. Length of teeth.--3.8 mm. Ratio length/width of teeth.--About 1:1.6. General shape of petiole sinus.--Y-shaped. Tooth at petiole sinus.--Absent. Petiole sinus limited byveins.--Absent. Shape of upper lateral sinus.--Open Y-shaped. Prostrate hairs between veins on lower surface of blade.--Absent. Erect hairs between veins on lower surface of blade.--Absent. Prostrate hairs on main veins on lower surface ofblade.--Present. Density of erect hairs on main veins on lower surface of blade.--Sparse. Prostrate hairs on main veins on upper surface of blade.--Absent. Upper surface: Summer color.--Civette green, 31' Y-G. Plate XVIII. Autumn color.--Variety'sGreen, 31'. Y-G Plate XVIII. Surface texture.--Smooth. Surface appearance.--Medium glossy. Goffering of blade.--Medium on mature leaves. Lower surface: Summer color.--Mineral green, 31'. Y-G. i Plate XVIII. Autumn color.--Grass Green, 33. G-YGPlate VI. Anthocyanin coloration of main veins on lower leaf surface.--Clear Yellow Green, 31. YG Plate VI. Glossiness.--Low. Pubescence.--Mildly present. Surface texture.--Medium leathery. Surface appearance.--Dull. Petiole: Length ofpetiole.--5.8 cm -- mean of 10 petioles. Diameter.--2.2 mm -- mean of 10 petioles. Fall color.--Varies along petiole from Deer Rose Pink, 71. V-RR. Plate XII) to Amaranth Purple, 69. Rv-R Plate XII. Length of petiole compared to middle vein.--Infall petioles are about 50% to 100% longer than the vein. Density of prostrate hairs on petiole.--Sparse on young leaves; absent on mature leaves. Density of erect hairs on petiole.--Dense on young leaves. Shape of base of petiole sinus.--Mostly open,with inside outline ovate. TENDRILS Number.--Tendrils at all nodes above node #2; abort on older growth. Length.--14.8 cm. Diameter.--1.4 mm. Texture.--Smooth. Color.--Mineral green, 31'. Y-G. i Plate XVIII, with occasional Brown vinaceous,5'''.OO-R Plate XXXIX to Pale Veronese Green, 31'. Y-G, Plate XVIII. WOODY SHOOT Trunk: Trunk circumference.--0.4 cm. at 1 meter height. Mean of 10 plants. Shape.--Circular. Surface texture.--Smooth -- canes still young. Outer barkcolor.--Vinaceous Tawny, 11'' orange Plate XXVIII. Canes: Shape of canes in cross section.--Broadly elliptical. Internode length.--6.7 cm. Mean of 10 canes counting nodes #3-6. Width at node.--About 0.75 cm. Mean of 10 canes measuring nodes #3-6. Surface.--Smooth. Main color.--Bright Clalcedony Yellow, 25' YG-Y-i Plate XVII. Fall color.--Carob brown, 9'. OR-O Plate XIV. Lenticels.--Inconspicuous. Erect hairs on nodes.--Absent. Erect hairs on internodes.--Absent. Growth of axillaryshoots.--Moderately prolific. Shape of nodes in cross section.--Circular to broadly elliptical. Number.--Lateral shoots generally develop at all nodes above node #5. Length.--Grow to about 0.5 to 1 m. Diameter.--2.9 mm -- mean of 10 laterals. Internode length.--6.3 cm -- mean of 10 canes. Color.--Wintergreen, 33'.GY-G, Plate XVIII to Dark Maroon Purple, 71'.V-RR, Plate XXVI. Buds: Shape.--Conical. Length.--2.8 mm. -- mean of 9 buds node. Width.--3.2 mm. mean of 9 buds node. Color.--Vinaceous Tawny, 11'' orange Plate XXVIII. FLOWERS -- Data from mature field parent `Chancellor` plants General: Flower sex.--Perfect. Length of first inflorescence.--5.2 cm. -- Mean of 7 inflorescences. Position of first floweringnodes.--2-4. Number of inflorescences per shoot.--# 1 TO 2. Pedicel length.--2.3 mm. -- Mean of 10 pedicels. Calyptra color.--Light Turtle green, 31''. Y-G Plate XXXII. Ovary length.--1.5 mm. -- Mean of 10 ovaries. Ovary width.--1.2 mm. -- Meanof 10 ovaries. Ovary color.--Light fluorite green, 33''.GY-G., Plate XXXII. Filament length.--1.9 mm. Composite mean of single filaments each from 5 flowers. Filament color.--Pale Turtle Green, 31''. Y-G Plate XXXII. Anther length.--0.55 mm. Composite mean of 4 anthers each from 4 flowers. Anther color.--Cream color 19'.YO-Y. f Plate XVI. FRUIT Herbicide resistance: Significantly greater resistance to phenoxy herbicides (especially 2,4 diphenoxyacetic acid) than parent `Chancellor`grapevine. The resistance in the `Improved Chancellor` is due to its genetic modification to contain and express the tfdA coding sequence. Transgenic plants survived treatment with 0.5, 5, and 10 kg ha-1 of the 2-ethylhexyl ester of 2, 4-D. Theserates killed non-transgenic plants. References:

Anonymous. International Plant Genetic Resources Institute, 1997, ISBN 92-9043-352-3

Murashige, T. and F. Skoog. 1962. A revised medium for rapid growth and bio-assays with tobacco tissue cultures. Physiologia Plantarum, 15: 473-497.

Nistch, J. P. and C. Nistch. 1969. Haploid plants from pollen grains. Science, 163: 85-87.

Ridgeway, R. 1912. Color standards and color nomenclature. A. Hoen and Company, Baltimore, Md.

Skirvin, R. M., M. A. Norton, A. G. Otterbacher, R. Mulwa, B. Shoemaker, B. Aly, and E. Wahle. 2005. Grape varieties for the different regions of Illinois -- 2005. Proceedings 2005 Illinois Small Fruit & Strawberry Schools. NRES 7:29-40.

Other References

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  • Streber et al., (1989) “Transgenic Tobacco Plants Expressing a Bacterial Detoxifying Enzyme are Resistant to 2, 4-D,” Bio/Technology 7:811-816.
  • Streber et al. (1987) “Analysis, Cloning, and High Level Expression of 2, 4-Dichlorophenoxyacetate Monooxygenase Gene tfdA of Alcaligenes eutrophus JMP134,” J. Bacteriol. 169:2950-2955.
  • Skirvin et al. (2005) “Grape Varieties for the Different Regions of Illinois,” Proc 2005 Illinois Small Fruit and Strawberry Schools, NRES 7:29-40.
  • Robinson et al. (1978) “2, 4-D Herbicides in Central Washington,” J. Air Pollution Control Association 28:1015-1020.
  • Perl et al. (1996) “Regeneration and Transformation of Grape (Vitis vinifera L.),” Plant Tissue Culture Biotechnol. 2:187-193.
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  • Norton et al., (2001) “Micropropagation of ‘Norton’ Wine grape,” Hortechnology 11:18-20.
  • Motoike et al., (2002) “Development of Methods of Genetically Transform American Grape (Vitis×labruscana L. H. Baily),” J. Hortic. Sci. Biotechnol. 77:691-696.
  • Levenko et al., (2000) “Herbicide Resistant Transgenic Plants of Grapevine,” Acta Horticulturae 528:337-339.
  • Last et al., (1999) “A Detoxification Gene in Transgenic Nicotiana tabacum Confers 2, 4-D Tolerance,” Weed Sci. 47:401-404.
  • Iocco et al., (2001) “Genetic Transformation of Major Wine Grape Cultivars of Vitis vinifera L.,” Transgenic Res., 10:105-112.
  • Hellman, E.W. (1987) “Cultivar Sensivity of Grapevines to 2, 4-D,” Fruit Varieties J. 41:111-114.
  • Hellman et al., (1999) Preventing Phenoxy Herbicide Damage to Grape Vineyards, Oregon State University Extension Service, Printed from eesc.orst.edu/agcomwebfile/admat/html on the internet.
  • Hébert-Soulé et al. (1995) “Phosphinothricin Stimulates Somatic Embryogenesis in Grape (Vitis sp. L.),” Plant Cell Reports 14:380-384.
  • Hébert et al. (1993) “Optimization of Biolistic Transformation of Embryogenic Grape Cell Suspensions,” Plant Cell Reports 12:585-589.
  • Chien, M. (2001) “2, 4-D Herbicide Drift into Vineyards,” The Grapevine Newsletter, Jan. 2001, Penn. State Cooperative Extension Agency.
  • Bayley et al., (1992) “Engineering 2, 4-D Resistance into Cotton,” Theoretical Appl. Genetics 83:645-649.
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