Maize histone deacetylases and their use

Details Maize histone deacetylases and their use Maize histone deacetylases and their use

1999-03-31

2001-09-11

Park, Hankyel T. (Department: 1648)

Chemistry: molecular biology and microbiology

Micro-organism, per se ; compositions thereof; proces of...

Bacteria or actinomycetales; media therefor

C435S006120, C435S419000, C536S023200, C800S279000

Reexamination Certificate

active

06287843

ABSTRACT:

FIELD OF THE INVENTION
The invention relates to the field of the genetic manipulation of plants, particularly the modulation of gene activity in plants and increased disease resistance.
BACKGROUND OF THE INVENTION
Histones are the protein portion of a protein-DNA complex termed the nucleosome. The acetylation of the &Sgr;-amino group of specific lysines present in the amino termini of histones has been correlated with both increased and decreased gene activity.
Nucleosomes structurally organize chromosomal DNA to form chromatin. The degree of interaction between histones and DNA varies between regions undergoing transcription and regions not being transcribed. The histones in chromatin regions containing active promoters are often post-translationally modified with acetyl groups covalently attached to specific lysine residues.
Hyperacetylated histones are thought to adopt a chromatin structure that allows other proteins to bind promoter DNA and activate transcription. Inactive promoters are associated with hypoacetylated histones, and removal of the acetyl groups from histones in normally active chromatin will repress transcription in that region.
Histone deacetylase (HD), responsible for removing acetyl modifications, may be localized to promoters targeted for repression by other proteins that associate with HD and specifically bind regulatory elements in promoter DNA.
Crop losses from pathogen infections are substantial and consume considerable quantities of productive plant biomass. It is generally believed that plant pathogens must find a way to suppress elicitation, the mechanism by which an elicitor, a pathogen-derived compound, induces disease gene expression upon recognition by the host.
One necrotrophic pathogen, the filamentous fungus
Cochliobolus carbonum
race 1, synthesizes a cyclic tetrapeptide, HC-toxin. HC-toxin is absolutely required for pathogenicity and is a specific inhibitor of HD activity. Resistant maize genotypes produce an HC-toxin reductase encoded by the nuclear Hm locus, which abolishes toxin activity by reducing the ketone group. These plants develop small expanding lesions in response to inoculation with Tox2
+
isolates of
C. carbonum
, similar to the lesions formed by Tox2
−
isolates regardless of the host genotype. HC-toxin acts in a cytostatic manner. It is not toxic to plant cells and does not determine pathogenicity by simply killing host cells prior to colonization.
Acetylation thus plays a key role in gene activation and in some instances invasion by pathogens. Mechanisms are therefore needed to control acetylation that may control gene activity and potentially play a role in disease resistance.
SUMMARY OF THE INVENTION
Compositions and methods for modulating gene activity states are provided. The compositions comprise histone deacetylases and nucleotide sequences encoding these enzymes, as well as nucleotide sequences encoding the corresponding antisense sequences to the histone deacetylases. The nucleotide sequences can be used to transform plants and alter the histone acetylation, heterochromatin, chromatin assembly, and gene activity of the transformed plants. In this manner, transformed plants having altered gene activity and enhanced disease resistance can be obtained.
Additionally, compositions of the invention find use in screening for toxins that affect pathogenicity and in determining which disease response promoters are regulated by histone deacetylase.


REFERENCES:
Pipal et al., Accession No.: AFO45473, Submitted (Jan. 28, 1998) Microbiology-Medical School, University of Innsbruck, Jan. 1998.*
Harvey et al., BDGP / HHMI Drosophila EST Project, Accession No. AA941447, Jan. 1998.*
Jan. 1998, Dec. 1997.*
Taunton et al.,A Mammalian Histone Deacetylase Related to the Yeast Transcriptional Regulator Rpd3p, Science, Apr. 19, 1996, pp. 408-411, vol. 272.
De Rubertis et al.,The Histone Deacetylase RPD3 Counteracts Genomic Silencing in Drosophila and Yeast, Nature, Dec. 12, 1996, pp. 589-591, vol. 384.
Rundlett et al.,HDAI and RPD3 are Members of Distinct Yeast Histone Deacetylase Complexes That Regulate Silencing and Transcription, Proc. Natl. Acad. Sci. USA, Dec. 1996, pp. 14503-14508, vol. 93.
Lusser et al,Identification of Maize Histone Deacetylase HD2 as an Acidic Nucleolar Phosphoprotein, Science, Jul. 4, 1997, pp. 88-91, vol. 277.
Tomihama T et al.,Arabidopsis Thaliana Histone Deacetylase mRNA, EMBL Database Accession No. AFO14824, Aug. 23, 1997, XP002120447.
Rossi et al.,Zea Mays Putative Histone Deacetylase RPD3 mRNA, EMBL Database Accession No. AFO35815, Dec. 9, 1997, XP002120446.
Rundlett et al.,HDA1 and RPD3 are Members of Distinct Yeast Histone Deacetylase Complexes that Regulate Silencing and Transcription, Proc. Natl. Acad. Sci. USA, Dec. 1996, pp. 14503-14508, vol. 93, De.
Brosch et al.,Purification and Characterizaation of a High Molecular Weight Histone Deacetylase Complex(HD2)of Maize Embryos, Biochemistry, 1996, pp. 15907-15914, vol. 35, American Chemical Society.
Lusser etr al.,Identification of Maize Histone Deacetylase HD2 as an Acidic Nucleolar Phosphoprotein, Science, Jul. 4, 1997, pp. 88-90, vol. 277, www.sciencemag.org.
Rossi et al.,Identification and Characterisation of an RPD3 homologue from Maize(Zea mays L.)that is able to Complement an rpd3 Null Mutant of Saccharomyces Cerevisiae, Mol. Gen. Genet, 1998, pp. 288-296, vol. 258.
Ransom, R. and Walton, J.,Histone Hyperacetylation in Maize in Response to Treatment with HC-Toxin or Infection by the Filamentous Fungus Cochliobolus Carbonum, Plant Pysiol., 1997, pp. 1021-1027, vol. 115.
Pipal et al.,Zea Mays Histone Deacetylase(hd1 b)mRNA, EMBL Database Accession No. AFO45473, Jan. 29, 1999, XP002120448.

Affiliated with

Also associated with

Rating

Maize histone deacetylases and their use does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Maize histone deacetylases and their use, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Maize histone deacetylases and their use will most certainly appreciate the feedback.

Rate now

Comments { 0 }

Profile ID: LFUS-PAI-O-2481465