Use of anthocyanin genes to maintain male sterile plants

Multicellular living organisms and unmodified parts thereof and – Plant – seedling – plant seed – or plant part – per se – Higher plant – seedling – plant seed – or plant part

Patent

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

800271, 800274, 8003201, A01H 500, A01H 400, A01H 100, C12N 504

Patent

active

060084375

DESCRIPTION:

BRIEF SUMMARY
The present invention relates to a method to maintain male-sterile plants that can be used for the production of hybrid seed of a plant crop species, to transgenic inbred plants that can be used in such process, and to chimeric genes that can be used to produce such transgenic inbred plants.


BACKGROUND OF THE INVENTION

In many, if not most plant species, the development of hybrid cultivars is highly desired because of their generally increased productivity due to heterosis: the superiority of performance of hybrid individuals compared with their parents (see e.g. Fehr, 1987, Principles of cultivar development, Volume 1 : Theory and Technique, MacMillan Publishing Company, New York; Allard, 1960, Principles of Plant Breeding, John Wiley and Sons, Inc.).
The development of hybrid cultivars of various plant species depends upon the capability of achieving essentially almost complete cross-pollination between parents. This is most simply achieved by rendering one of the parent lines male sterile (i.e. bringing them in a condition so that pollen is absent or nonfunctional) either manually, by removing the anthers, or genetically by using, in the one parent, cytoplasmic or nuclear genes that prevent anther and/or pollen development (for a review of the genetics of male sterility in plants see Kaul, 1988, `Male Sterility in Higher Plants`, Springer Verlag).
For hybrid plants where the seed is the harvested product (e.g. corn, oilseed rape) it is in most cases also necessary to ensure that fertility of the hybrid plants is fully restored. In systems in which the male sterility is under genetic control this requires the existence and use of genes that can restore male fertility. The development of hybrid cultivars is mainly dependent on the availability of suitable and effective sterility and restorer genes.
Endogenous nuclear loci are known for most plant species that may contain genotypes which effect male sterility, and generally, such loci need to be homozygous for particular recessive alleles in order to result in a male-sterile phenotype. The presence of a dominant `male fertile` allele at such loci results in male fertility.
Recently it has been shown that male sterility can be induced in a plant by providing the genome of the plant with a chimeric male-sterility gene comprising a DNA sequence (or male-sterility DNA) coding, for example, for a cytotoxic product (such as an RNase) and under the control of a promoter which is predominantly active in selected tissue of the male reproductive organs. In this regard stamen-specific promoters, such as the promoter of the TA29 gene of Nicotiana tabacum, have been shown to be particularly useful for this purpose (Mariani et al., 1990, Nature 347:737, European patent publication ("EP") 0,344,029). By providing the nuclear genome of the plant with such a male-sterility gene, an artificial male-sterility locus is created containing the artificial male- sterility genotype that results in a male-sterile plant.
In addition it has been shown that male fertility can be restored to the plant with a chimeric fertility-restorer gene comprising another DNA sequence (or fertility-restorer DNA) that codes, for example, for a protein that inhibits the activity of the cytotoxic product or otherwise prevents the cytotoxic product from being active in the plant cells (European patent publication "EP" 0,412,911). For example the barnase gene of Bacillus amyloliquefaciens codes for an RNase, called barnase, which can be inhibited by a protein, barstar, that is encoded by the barstar gene of B. amyloliquefaciens. The barnase gene can be used for the construction of a sterility gene while the barstar gene can be used for the construction of a fertility-restorer gene. Experiments in different plant species, e.g. oilseed rape, have shown that a chimeric barstar gene can fully restore the male fertility of male sterile lines in which the male sterility was due to the presence of a chimeric barnase gene (EP 0,412,911, Mariani et al., 1991, Proceedings of the CCIRC Rapeseed Congress, Jul. 9

REFERENCES:
patent: 3842538 (1974-10-01), Barabas
patent: 4727219 (1988-02-01), Brar et al.
patent: 5356799 (1994-10-01), Fabijanski et al.
patent: 5525716 (1996-06-01), Olsen et al.
Nature, "A Chimaeric Ribonuclease-Inhibitor Gene Restores Fertility to Male Sterile Plants", C. Mariani, et al., vol. 357, pp. 384-387, Jun. 4, 1992.
"The Mutants of Maize", M. Neuffer, et al., Published by the Crop Science Society of America, pp. 67-68.
"Breeding Field Crops", Third Edition, J. Poehlman, pp. 473-476.
V. Chandler, et al. "Two Regulatory Genes of the Maize Anthocyanin Pathway are Homologous: Isolation of B Utilizing R Genomic Sequences", The Plant Cell (1989) 1:1175-1183.
E. Coe, "Anthocyanin Genetics", The Maze Handbook (1994) pp. 279-281.
K. Cone et al., "Maize Anthocyanin Regulatory Gene pi is a Duplicate of c1 that Functions in the Plant", The Plant Cell (1993) 5:1795-1805.
G. Consonni et al., "Molecular Homology Among Members of the R Gene Family in Maize", The Plant Journal (1993)3:335-346, No. 2.
H. Dooner et al., "Genetic and Developmental Control of Anthocyanin Biosynthesis", Annu. Rev. Genet (1991) 25:173-99.
W. Galinat, "Use of Male-Sterile 1 Gene to Eliminate Detasseling in Production of Hybrid Seed of Bicolor Sweet Corn", The Journal of Heredity (1975) 66:387-388.
S. Goff et al., "Functional Analysis of the Transcriptional Activator Encoded by the Maize B Gene: Evidence for a Direct Functional Interaction Between Two Classes of Regulatory Proteins", Genes & Development (1992) 6:864-875.
S. Goff et al., "Identification of Functional Domains in the Maize Transcriptional Activator C1: Comparison of Wild-Type and Dominant Inhibitor Proteins", Genes& Development (1991) 5:298-309.
J. Goodrich et al., "A Common Gene Regulates Pigmentation Pattern in Diverse Plant Species", Cell (1992) 68:955-964.
Hartley, "Barnase and Barstar--Expression of Its Clones Inhibitor Permits Expression of a Cloned Ribonuclease", J. Mol. Biol. (1988) 202:913-915.
Ch. Jayaram et al., "Anthocyanin Pigmentation and Transposable Elements in Maize Aleurone", Plant Breeding Reviews (1990) 8:91-137.
K. Kaukis et al., "Sweet Corn Breeding", Breeding Vegetable Crops (1986) pp. 475-598.
T. Klein, "Regulation of Antocyanin Biosynthetic Genes Introduced into Intact Maize Tissues by Microprojectiles", Proc. Natl. Acad. Sci. (1989) 86:6681-6685.
S. Ludwig, "Lc, a Member of the Maize R Gene Family Responsible for Tissue-Specific Anthocyanin Production, Encodes a Protein Similar to Transcriptional Activators and Contains a myc-homology Region", Proc. Natl. Acad. Sci. (1989) 86:7092-7096.
J. Paz-Ares et al., "The Regulatory c1 Locus of Zea mays Encodes a Protein With Homology to myb Proto-oncogene Products and with Structural Similarities to Transcriptional Activators", The EMBO Journal (1987) 6:3553-3558, No. 12.
J. Paz-Ares et al. "Molecular Analysis of the C1-1 allele from Zea mays: a Dominant Mutant of the Regulatory C1 Locus", The EMBO Journal (1990) 9: 315-321, No. 2.
G. Perrot et al. "Nucleotide Sequence of the Maize R-S Gene", Nucleic Acids Research (1989) 17:8003, No. 19.
F. Quattrocchio et al., "Regulatory Genes Controlling Anthocyanin Pigmentation Are Functionally Conserved Among Plant Species and Have Distinct Sets of Target Genes", The Plant Cell (1993) 5: 1497-1512.
J. P. Radicella et al., "Cloning and Nucleotide Sequence of a cDNA encoding B-Peru, a Regulatory Protein of the Anthocyanin Pathway in Maize", Plant Molecular Biology (1991) 17:127-130.
J.P. Radicella et al., "Allelic Diversity of the Maize B Regulatory Gene: Different Leader and Promoter Sequences of two B Alleles Determine Distinct Tissue Specificities of Anthocyanin Production", Genes & Development (1992) 6:2152-2164.
B. Scheffler, "Molecular Analysis of C1 Alleles in Zea mays Defines Regions Involved in the Expression of This Regulatory Gene", Mol. Gen. Genet (1994) 242:40-48.
N. Stoskopf, "Plant Breeding: Theory and Practice"Westview Press, Chapter 22, pp. 453-472.
Mariani et al., "Induction of Male Sterility in Pl

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Use of anthocyanin genes to maintain male sterile plants does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Use of anthocyanin genes to maintain male sterile plants, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Use of anthocyanin genes to maintain male sterile plants will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-2383589

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.