Regulation of embryonic transcription in 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

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C800S278000, C800S287000, C800S281000, C536S024100, C435S468000, C435S419000, C435S320100

Reexamination Certificate

active

06784342

ABSTRACT:

FIELD OF THE INVENTION
The invention is in the field of nucleic acid sequences capable of regulating transcription, particularly sequences that may promote transcription during embryogenesis in plants.
BACKGROUND OF THE INVENTION
Most of the information about seed-specific gene expression comes from studies of genes encoding seed storage proteins like napin, a major protein in the seeds of
Brassica napus,
or conglycinin of soybean. Upstream DNA sequences directing strong embryo-specific expression of these storage proteins have been used successfully in transgenic plants to manipulate seed lipid composition and accumulation (Voelker et al., 1996). However, expression of storage protein genes begins fairly late in embryogenesis. Thus, promoters of seed storage protein genes may not be ideal for all seed-specific applications. For example, storage oil accumulation commences significantly before the highest level of expression of either napin (Stalberg et al., 1996) or conglycinin (Chen et al., 1988) is achieved. It is, therefore of interest to identify other promoters which may modulate expression of genes in developing plant embryos.
A variety of transcriptional regulatory regions that may be active during plant embryogenesis are known, as disclosed for example in: U.S. Pat. No. 5,792,922 issued Aug. 11, 1998 to Moloney; U.S. Pat. No. 5,623,067 issued Apr. 22, 1997 to Vandkerckhove et al.; International Patent Publication WO9845461 published Oct. 15, 1998. There remains a need for alternative transcriptional regulatory regions.
FATTY ACID ELONGATION1 (FAE1) genes encode condensing enzymes involved in plant very long chain fatty acid biosynthesis. The FAE1 condensing enzyme is thought to be localized in the endoplasmic reticulum where it catalyzes the sequential elongation of C18 fatty acyl chains to C22 in length (Kunst et al., 1992). FAE1 genes have been cloned and described recently by James et al. (1995), International Patent Publication WO 96/13582.
SUMMARY OF THE INVENTION
In one aspect, the invention provides transcriptional regulatory regions derived from FAE1 genes. The transcriptional regulatory regions of the invention may be useful in promoting early seed-specific transcription of heterologous sequences to which they are operably linked. The transcriptional regulatory regions of the invention may be used in a wide variety of plants, including Brassica sp., Arabidopsis and other plant species. DNA constructs comprising the transcriptional regulatory sequences of the invention may be active during fatty acid or lipid biosynthesis in the plant embryo. Certain embodiments of the constructs of the invention may be used in transgenic plants to promote expression of heterologous sequences in developing seeds. In various embodiments, the constructs of the invention may be used to mediate gene expression that affects seed lipid metabolism, or seed protein composition or seed carbohydrate composition, or seed development. In alternative embodiments, the transcriptional regulatory regions of the invention may also be useful for the production of modified seeds containing novel recombinant proteins which have pharmaceutical, industrial or nutritional value.


REFERENCES:
patent: 5623067 (1997-04-01), Vandekerckhove et al.
patent: 5792922 (1998-08-01), Maloney
patent: WO 9515387 (1995-06-01), None
patent: WO 9613582 (1996-05-01), None
patent: WO 98/45461 (1998-10-01), None
patent: WO 9846766 (1998-10-01), None
patent: WO 9854954 (1998-12-01), None
patent: WO 9903983 (1999-01-01), None
patent: WO 9954471 (1999-10-01), None
Sindhu et al., The pea seed storge protein legumin was synthesized, processed, and accumlated stably in transgenic rice endosperm, 1997. Plant Science, vol. 130, pp. 189-196.*
Lohmann et al., A Molecular Link between Stem Cell Regulation and Floral Patterning in Arabidipsis. Jun. 15, 2001, Cell, vol. 105, pp. 793-803.*
Busch et al., Activation of a Floral Homeotic Gene in Arabidopsis. Jul. 23, 1999. Science vol. 285, pp. 585-587.*
Izawa et al., Plant bZIP Protein DNA Binding Specificity, 1993. J Mol. Biol., vol. 230, pp. 1131-1144.*
Hao et al., Unique Mode of GCC Box Recognition by the DNA-binding Domain of . . . Oct. 9, 1998, The Journal of Biological Chemistry, vol. 273, No. 41, pp. 26857-26861.*
Eshed et al., Establisment of polarity in lateral organs of plants. 2001, Current Biology, vol. 11, pp. 1251-1260.*
Finnegan et al., Transgene Inactivation: Plant Fight Back!, Sep. 1994. Bio/Technology, vol. 12, pp. 883-887.*
Benfey et al., “Regulated genes in transgenic plants,”Science244:174-181, 1989.
Beyan et al., “Tissue- and cell-specific activity of a phenylalanine ammonia-lyase promoter in transgenic plants,”EMBO J.8:1899-1906, 1989.
Katavic et al., “In plantatransformation ofArabidopsis thaliana ,” Mol. Gen. Genet.245:363-370, 1994.
Konez et al., “The promoter of TL-DNA gene 5 controls the tissue-specific expression of chimaeric genes carried by a novel type ofAgrobacteriumbinary vector,”Mol. Gen. Genet.204:383-396, 1986.
Lee et al., “Manipulation of plant gene expression using antisense RNA,” In:Plant Biochemistry/Molecular Laboratory Manualpp. 423-439, Dashek, WV. ed., CRC Press. Inc. Boca Raton, 1996.
Murphy et al., “Immunocytochemical and biochemical study of the biosynthesis and mobilisation of the major seed storage proteins ofBrassica napus, ” Plant. Physiol. Biochem.27:647-657, 1989.
Stalberg et al., “Disruption of an overlapping E-box-ABRE motif abolished high transcription of the napA storage-protein promoter in transgenicBrassica napusseed, ”Plant199:515-519, 1996.
Voelker et al., “Genetic engineering of a quantitative trait: metabolic and genetic parameters influencing the accumulation of laurate in rapeseed,”Plant J.9:229-241, 1996.
Rowley et al., “The upstream domain of soybean olesin genes contains regulatory elements similar to those of legume storage proteins, ”Biochim. Biophys. Acta1345:1-4, 1997.
Morton et al., “Regulation of Seed Storage Protein Gene Expression,” Kigel and Gallili, eds., pp. 103-138, Marcel Dekker, New York, 1994.
Kawagoe et al., “Four distinct nuclear proteins recognize in vitro proximal promoter of the bean seed storage protein &bgr;-phaseolin gene conferring spatial and temporal control,”Plant J.2:927-936, 1992.
Shen et al., “Functional Dissection of an Abscisc Acid (ABA)—Inducible GeneReveals Two Independent ABA—Responsive Complexes Each Containing a G-Boxand a Novel cis-Acting Element,”Plant Cell7:295-307, 1995.
Dickinson et al., “RY repeats are conserved in the 5′-flakning regions of legume seed-protein genes,”Nucleic Acid Res., 16:371, 1988.
Lelievre et al., “5′-CATGCAT-3′Elements Modulate the Expression of Glycinin Genes”Plant Physiol. 98:387-391, 1992.
Chen et al., “A DNA sequence element that confers seed-specific enhancement to a constitutive promoter,”EMBO J.7:297-302, 1988.
Shen et al., “Modular Nature of Abscisic Acid (ABA) Response Complexes: Composite Promoter Units That Are Neccessary and Sufficient for ABA Induction of Gene Expression in Barley,”Plant Cell8:1107-1119, 1996.
James et al., “Directed Tagging of the ArabidopsisFatty Acid Elongation(FAE1) Gene with the Maize Transposon Activator,”Plant Cell7:309-319, Mar. 1995.
Kunst et al., “Fatty acid elongatio in developing seeds ofArabidopsis thaliana,” Plant Physiol. Biochem.30(2):425-434, 1992.
Millar et al., “CUT1, an Arabidopsis Gene Required for Cuticular Wax Biosynthesis and Pollen Fertility, Encodes a Very-Long-Chain Fatty Acid Condensing Enzyme,”Plant Cell11:825-838, May 1999.
Clemens and Kunst, Accession No. AF009563, Jul. 24, 1997.
James et al., Accession No. U29142, Jul. 4, 1995.
Roscoe et al., Accession No. U50771, Apr. 6, 1996.
Venkateswari et al., “Molecular Cloning and Characterization ofFatty Acid Elongation(BjFAE1)gene of Brassica juncea,”J. Plant Biochem. Biotech.8(1):53-55, Jan. 1999.

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

Regulation of embryonic transcription in 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 Regulation of embryonic transcription in plants, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Regulation of embryonic transcription in plants will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-3343659

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