AU758678B2 - Plant sugar sensors and uses thereof - Google Patents

Description

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AUSTRALIA

Patents Act 1990 COMPLETE SPECIFICATION STANDARD PATENT Applicant(s) THE GENERAL HOSPITAL CORPORATION Invention Title: PLANT SUGAR SENSORS AND USES THEREOF The following statement is a full description of this invention, including the best method of performing it known to me/us: PLANT SUGAR SENSORS AND USES THEREOF Background of the Invention This application relates to plant carbohydrate metabolism; in particular, to enzymes which transduce sugar-sensing signals, their encoding genes, and uses thereof.

Sugars are said to be regulatory molecules that are capable of controlling physiology, metabolism, cell cycle, development, and gene expression. Throughout the higher plant life cycle, from germination to flowering to senescence, sugars affect growth and development. Recently, it has become apparent that sugars are physiological signals capable of repressing or activating plant genes that are involved in many essential processes, including photosynthesis, the glyoxylate cycle, respiration, starch and sucrose synthesis and degradation, nitrogen metabolism and storage, pathogen defense, the wounding response, cell cycle progression, pigmentation, and senescence (Sheen, Photosynthesis Res. 39,427 (1994); Thomas and Rodriguez, Plant Physiol. 106, 1235 (1994); Knight and Gray, Mol. Gen. Genet.

242, 586 (1994); Lam et al., Plant Physiol. 106, 1347 (1994); Chen et al., PlantJ. 6, 20 625 (1994); Reynolds and Smith, Plant Mol. Biol. 29, 885 (1995); Herbers et al., Plant Mol. Biol. 29, 1027 (1995); Mita et al., Plant Physiol. 107,895 (1995)).

Studies in a variety of plant species have also shown that sugar homeostasis appears to be tightly regulated. Elevated sugar concentration leads to stunted growth, reduced photosynthesis, leaf curling, chlorosis, necrotic leaves, and anthocyanin accumulation 25 (Casper et al., Plant Physiol. 79, 11 (1985); von Schaewen et al., EMBO J. 9, 3033 (1990); Dickinson et al., Plant Physiol. 95, 420 (1991); Tsukaya et al., Plant Physiol.

97, 1414 (1991); Sonnewald et al., Plant J. 1, 95 (1991); Huberet and Hanson, Plant Physiol. 99, 1449 (1992); Sonnewald et al., Plant Responses to Sugar Accumulation in Transgenic Tobacco Plants, pp. 246-257, In: M. A. Madore, W. J. Lucas (eds.), 3 0 Carbon Partitioning and Source-Sink Interactions in Plants, American Society of 2 Plant Physiologists, Rockville, MD, (1995)). In addition, environmental factors such as elevated CO 2 and intrinsic genetic variations such as different invertase levels have been proposed to affect photosynthetic capacity through sugar regulation (Stitt, Plant Cell Environ. 14, 741 (1991); Stitt et al., Planta 183, 40 (1991); VanOosten et al., Plant Cell Environ. 17, 913 (1994); Nie et al., Plant Physiol. 108, 975 (1995); Goldschmidt and Huber, Plant Physiol. 99, 1443 (1992)).

It will be clearly understood that, although a number of prior art publications are referred to herein, this reference does not constitute an admission that any of these documents forms part of the common general knowledge in the art, in Australia or in any other country.

Summary of the Invention By manipulating the expression of a plant hexokinase protein (HXK), we have discovered that this protein is a sensor that mediates diverse sugar responses in plants. In particular, we have engineered transgenic 20 plants that either: express a decreased level of hexokinase protein due to expression of an antisense hexokinase gene and therefore exhibit a decreased sensitivity to sugar; or express an increased level of hexokinase protein and therefore exhibit an increased sensitivity to sugar. Our discovery has broad implications for the manipulation of agricultural crops, for increasing crop yield and quality, and for reducing production costs.

In general, the invention features a method for reducing the level of a plant hexokinase protein in a transgenic 30 plant cell, the method involving expressing in the transgenic plant cell (for example, a cell from a monocot, a dicot, or a gymnosperm) an antisense hexokinase nucleic acid sequence. This produces transgenic plants that are less sensitive to sugar (for example, glucose, sucrose, fructose or mannose).

In preferred embodiments, the antisense hexokinase nucleic acid sequence is encoded by a transgene H:\cintae\Keep\speci\23429.97 div.doc 17/10/00 2a integrated into the genome of the transgenic plant cell; the antisense hexokinase nucleic acid sequence includes a plant antisense hexokinase DNA sequence (for example, a sequence that is based on the AtHXKl nucleotide sequence of Fig. 1F (SEQ ID NO:3) or the AtHXK2 nucleotide sequence of Fig. 1G (SEQ ID and the method further includes growing a transgenic plant from the transgenic plant cell, whereby the level of the hexokinase protein is reduced in the transgenic plant.

e e H:\cintae\Keep\speci\23429.97 div.doc 17/10/00 Ij In related aspects, the invention features a plant cell (for example, a plant cell from a monocot, dicot, or gymnosperm) expressing an antisense hexokinase nucleic acid sequence; and a plant expression vector including an antisense hexokinase nucleic acid sequence, wherein the sequence is operably linked to an expression control region.

In yet another aspect, the invention features a method for increasing the level of a hexokinase protein in a transgenic plant cell, involving expressing in the transgenic plant cell a hexokinase nucleic acid sequence. In preferred embodiments, the hexokinase nucleic acid sequence is from a plant (for example, a DNA sequence that is identical to the AtHXK1 nucleotide sequence of Fig. IF (SEQ ID NO: 3) or that is substantially identical to the AtHXK2 nucleic acid sequence of Fig. I G (SEQ ID NO: This method produces transgenic plants having an increased sensitivity to sugar.

In related aspects, the invention features a substantially pure plant HXK polypeptide including an amino acid sequence substantially identical to the amino acid sequence of AtHXKI (SEQ ID NO: 1) or AtHXK2 (SEQ ID NO: In preferred embodiments of both of these aspects, the HXK polypeptide is obtained from a plant including, but not limited to, a monocot (for example, rice, corn, wheat, or barley), a dicot (for example, a member of the Solanaceae (for example, potatoes) 20 or a member of the Cruciferae (for example, Arabidopsis, broccoli, cabbage, brussel sprouts, rapeseed, kale, Chinese kale, cauliflower, or horseradish)), and a gymnosperm.

In yet other related aspects, the invention features a substantially pure DNA encoding a plant HXK polypeptide that includes an amino acid sequence substantially identical to the amino acid sequence of AtHXKl (SEQ ID NO: 1) or AtHXK2 (SEQ ID NO: In preferred embodiments, the DNA includes the nucleotide sequence shown in Fig. IF (SEQ ID NO: 3) or includes a nucleotide sequence that is substantially identical to the sequence that is shown in Fig. 1G (SEQ ID NO: 4).

Such DNAs are obtained from any plant including, but not limited to, a monocot (for -3-

I

example, rice, corn, wheat, and barley), a dicot (for example, a member of the Solanaceae (for example, potatoes) or a member of the Cruciferae (for example, Arabidopsis, broccoli, cabbage, brussel sprouts, rapeseed, kale, Chinese kale, cauliflower, or horseradish)), and a gymnosperm. In other preferred embodiments, the DNAs of the invention are operably linked to a constitutive or regulated promoter.

In yet other related aspects, the invention features a vector including any of the substantially pure DNAs of the invention, the vector being capable of directing expression of the protein encoded by the DNA in a vector-containing cell; a cell, for example, a prokaryotic cell (for example, an E. coli cell) or a eukaryotic cell (for example, a plant cell) which includes any of the DNAs of the invention; and a transgenic plant (or a cell or a seed derived from such a transgenic plant) including any of the DNAs of the invention integrated into the genome of the plant, wherein the DNA is expressed in the transgenic plant.

In various preferred embodiments, the plant cell contains the DNA in the sense orientation and has an increased sensitivity to sugar, the plant cell contains the DNA in the antisense orientation and is less sensitive to sugar; and the DNA is expressed under the control of a constitutive promoter or regulated promoters.

In two other aspects, the invention features a method of producing a plant HXK polypeptide involving: providing a cell transformed with a gene encoding a 20 polypeptide including either an amino acid sequence substantially identical to the amino acid sequence ofAtHXKl (SEQ ID NO: 1)or an amino acid sequence substantially identical to the amino acid sequence of AtHXK2 (SEQ ID NO: 2) positioned for expression in the cell; expressing the plant HXK polypeptide; and recovering the plant HXK polypeptide.

By "hexokinase" or "HXK" is meant a polypeptide that is capable of S" catalyzing the ATP-dependent conversion ofhexoses to hexose-6-phosphates.

Methods for assaying such enzymatic activities are known in the art, those described herein by Renz and Stitt (Planta 190, 166 (1993)).

decie eenb•ezadSit(lna1016(93) By "reducing the level of a plant hexokinase protein" is meant a decrease in the level of that plant hexokinase protein by at least 30-50%, preferably by 50-80%, and more preferably by 80-95% relative to the level in a control plant (for example, a wild-type plant). Reduction of hexokinase protein levels may be accomplished through the expression of an antisense plant hexokinase nucleotide sequence in a transgenic plant. Levels of plant hexokinase protein are monitored according to any standard technique including, but not limited to, immunoblotting (for example, as described herein). Alternatively, the level of a plant hexokinase protein may be quantified according to standard hexose phosphorylation assays (for example, those described herein).

By "increasing the level of a plant hexokinase protein" is meant increasing the level of that plant hexokinase protein by at least 50%, preferably 100%, and more preferably greater than 200% relative to the level in a control plant (for example, a wild-type plant). Levels of plant hexokinase protein are monitored according to any standard technique including, but not limited to, immunoblotting (for example, as described herein). Alternatively, the level of a plant hexokinase protein may be quantified according to standard hexose phosphorylation assays (for example, those described herein).

By "an antisense hexokinase sequence" is meant a nucleotide sequence that is 20 complementary to a plant hexokinase messenger RNA. In general, such an antisense sequence will usually be at least 15 nucleotides, preferably about 15-200 nucleotides, and more preferably 200-2,000 nucleotides in length. The antisense sequence may be S complementary to all or a portion of the plant hexokinase mRNA nucleotide sequence (for example, the AtHXK1 and AtHXK2 antisense constructs described herein), and, as appreciated by those skilled in the art, the particular site or sites to which the antisense sequence binds as well as the length of the antisense sequence will vary, .depending upon the degree of inhibition desired and the uniqueness of the antisense sequence. A transcriptional construct expressing a plant hexokinase antisense nucleotide sequence includes, in the direction of transcription, a promoter, the q sequence coding for the antisense RNA on the sense strand, and a transcriptional termination region. Antisense HXK sequences may be constructed and expressed as described herein or as described, for example, in van der Krol et al., Gene 72, (1988); Rodermel et al., Cell 55, 673 (1988); Mol et al., FEBSLett. 268,427 (1990); Weigel and Nilsson, Nature 377, 495 (1995); Cheung et al., Cell 82, 383 (1995); and U.S. Pat. No. 5,107,065.

By "less sensitive to sugar" is meant that the developmental, physiological, or molecular processes that are typically regulated or controlled by internal or external sugar concentrations exhibit reduced responses to the presence of a sugar (for example, glucose, fructose, mannose, or sucrose). For example, a plant having reduced sensitivity to sugar is capable of activating an assortment of genes (for example, photosynthetic genes) that are normally repressed by the presence of sugar, or such a plant is capable of proceeding through its normal developmental pathway even in the presence of sugar concentrations that would otherwise thwart or prevent such development. Analysis of a plant's sensitivity to sugar is accomplished using a wide variety of bioassays (for example, those described herein). These assays include, but are not limited to, evaluating and monitoring gene expression, seed germination, cotyledon development (for example, cotyledon extension), cotyledon greening, leaf development, embryonic root development, hypocotyl elongation, 20 anthocyanin accumulation, starch accumulation, and time needed for flowering. By comparing phenotypes of wild-type plants and candidate plants (for example, a plant expressing an antisense hexokinase gene), one is readily able to determine whether such a candidate transgenic plant has a reduced sensitivity to a sugar. For example, sugars have been found to repress the expression of both photosynthetic (for example, 25 ribulose bisphosphate carboxylase small subunit and light-harvesting chlorophyll a/b binding protein) and non-photosynthetic (for example, a-amylase, sucrose synthase, malate synthase, and asparagine synthase) genes. Thus, in plants that are less sensitive to sugar, the aforementioned sugar-repressible genes have a decreased, reduced, or attenuated level of sugar-mediated repression.

By "increased sensitivity" is meant that the developmental, physiological, or molecular processes that are typically regulated or controlled by internal or external sugar concentrations exhibit increased or elevated responses to the presence of a sugar (for example, glucose, fructose, mannose, or sucrose). For example, a plant having increased sensitivity to sugar is capable of elevating, raising, or promoting the activation of an assortment of genes (for example, vegetative storage proteins) that are normally activated by the presence of sugar. Analysis of a plant's sensitivity to sugar is accomplished using a wide variety of bioassays. These assays include, but are not limited to, evaluating and monitoring gene expression, seed germination, cotyledon development (for example, cotyledon extension), cotyledon greening, leaf development, embryonic root development, hypocotyl elongation, anthocyanin accumulation, starch accumulation, and time needed for flowering. By comparing phenotypes of wild-type plants and candidate plants (for example, a plant expressing at least one additional copy ofhexokinase gene), one is readily able to determine whether such a candidate transgenic plant has an increased sensitivity to a sugar. For example, sugars have been found to activate the expression of genes such as nitrate reductase, P-amylase, sucrose synthase, and potato storage protein. Thus, in plants exhibiting an increased sensitivity to sugar, the aforementioned sugar-inducible genes have an increased, elevated, or heightened level of sugar-mediated expression.

S: 20 By "polypeptide" or "protein" is meant any chain of amino acids, regardless of length or post-translational modification (for example, glycosylation or phosphorylation).

By "substantially identical to AtHXKl" is meant a plant hexokinase polypeptide that includes an N-terminus which is at least 50%, preferably 75%, more 25 preferably 85-90%, and most preferably 95% identical to the N-terminus of AtHXK1 •(amino acids 1-61 of Fig. 1B; SEQ ID NO:l). The length of comparison will generally be at least 15 amino acids, preferably at least 30 amino acids, more preferably at least 40 amino acids, and most preferably 60 amino acids.

By "substantially identical to AtHXK2" is meant a plant hexokinase polypeptide or nucleic acid sequence that exhibits at least 86%, preferably 90%, more preferably 95%, and most preferably 99% identity to the amino acid or nucleic acid sequences of AtHXK2 (Figs. IB and 10; SEQ ID NOS: 2 and 4).

Sequence identity is typically measured using sequence analysis software (for example, Sequence Analysis Software Package of the Genetics Computer Group (University of Wisconsin Biotechnology Center, 1710 University Avenue, Madison, WI 53705), BLAST, or PILEUP/PRETTYBOX programs). Such software matches similar sequences by assigning degrees of homology to various substitutions, deletions, substitutions, and other modifications. Conservative substitutions typically include substitutions within the following groups: glycine alanine; valine, isoleucine, leucine; aspartic acid, glutamic acid, asparagine, glutamine; serine, threonine; lysine, arginine; and phenylalanine, tyrosine.

By a "substantially pure polypeptide" is meant a plant hexokinase polypeptide (for example, AtHXKl or AtHXK2) which has been separated from components which naturally accompany it. Typically, the polypeptide is substantially pure when it is at least 6 0 by weight, free from the proteins and naturally-occurring organic molecules with which it is naturally associated. Preferably, the preparation is at least more preferably at least 90%, and most preferably at least 99%, by weight, plant 20 hexokinase polypeptide. A substantially pure plant hexokinase polypeptide may be obtained, for example, by extraction from a natural source (for example, a plant cell); Sby expression of a recombinant nucleic acid encoding a plant hexokinase polypeptide; or by chemically synthesizing the protein. Purity can be measured by any appropriate method, for example, column chromatography, polyacrylamide gel electrophoresis, or HPLC analysis.

By "substantially pure DNA" is meant DNA that is free of the genes which, in the naturally-occurring genome of the organism from which the DNA of the invention is derived, flank the gene. The term therefore includes, for example, a recombinant DNA which is incorporated into a vector, into an autonomously replicating plasmid or virus; or into the genomic DNA of a prokaryote or eukaryote; or which exists as a separate molecule (for example, a cDNA or a genomic or cDNA fragment produced by PCR or restriction endonuclease digestion) independent of other sequences. It also includes a recombinant DNA which is part of a hybrid gene encoding additional polypeptide sequence.

By "transformed cell" is meant a cell into which (or into an ancestor of which) has been introduced, by means of recombinant DNA techniques, a DNA molecule encoding (as used herein) an HXK polypeptide (for example, AtHXKI or AtHXK2).

By "positioned for expression" is meant that the DNA molecule is positioned adjacent to a DNA sequence which directs transcription and translation of the sequence facilitates the production of, for example, a plant hexokinase polypeptide such as AtHXK1 or AtHXK2, a recombinant protein, or a RNA molecule).

By "promoter" is meant a minimal sequence sufficient to direct transcription, Included in the invention are promoter elements that are sufficient to render promoterdependent gene expression controllable for cell-, tissue-, or organ-specific gene expression, or elements that are inducible by external signals or agents (for example, light-, pathogen-, wound-, or hormone-inducible elements); such elements may be located in the 5' or 3' regions of the native gene.

20 By "operably linked" is meant that a gene and a regulatory sequence(s) are connected in such a way as to permit gene expression when the appropriate molecules (for example, transcriptional activator proteins) are bound to the regulatory sequence(s).

By "plant cell" is meant any self-propagating cell bounded by a semipermeable membrane and containing a plastid. Such a cell also requires a cell wall if i further propagation is desired. Plant cell, as used herein includes, without limitation, algae, cyanobacteria, seeds, suspension cultures, embryos, meristematic regions, callus tissue, leaves, roots, shoots, gametophytes, sporophytes, pollen, and microspores.

10 By "transgene" is meant any piece of DNA which is inserted by artifice into a cell, and becomes part of the genome of the organism which develops from that cell. Such a transgene organism may include a gene which is partly or entirely heterologous foreign) to the transgenic organism, or may represent a gene homologous to an endogenous gene of the organism.

By "transgenic" is meant any cell which includes a DNA sequence which is inserted by artifice into a cell and becomes part of the genome of the organism which develops from that cell. As used herein, the transgenic organisms are generally transgenic plants and the DNA (transgene) is inserted by artifice into the nuclear or plastidic genomes.

Other features and advantages of the invention will be apparent from the following description of the preferred embodiments thereof, and from the claims.

Throughout the description and claims of this specification, the word "comprise" and variations of the word, such as "comprising" and "comprises", means "including but not limited to", and is not intended to exclude other additives, components, integers or steps.

Detailed Description The drawings will first be described.

Drawings Figs. 1A-E are illustrations showing various aspects of the molecular characterisation of the Arabidopsis thaliana HXK genes. Fig. 1A shows the functional complementation HXK catalytic activity using a yeast hxkl/hxk2 double mutant (designated DBY2219) with the A. thaliana HXK homologues, AtHXK1 and AtHXK2. pFL61 is shown as the control vector used in these complementation studies. Fig. 1B is a schematic illustration showing the amino acid sequence comparison of A. thaliana hexokinase \\.1lbilmhomS \,ainre\ ep\ect \vpmc 23429.97.doC 15/05/00 10a ALHXK1 (SEQ ID NO: A. thaliazna hexokinase ALHXK2 (SEQ ID NO: human GLK (SEQ ID NVO: rat GLK (SEQ ID No: Saccharomyces cerevisiae HXK1 (Yeastl) (SEQ ID NO: 7), S. cerevisiae HXK2 (Yeast2) (SEQ ID NO: and Kluveromyces lactis RAG5 (Yeast3) (SEQ ID NO: 9) The underlined regions 1 and 2 refer to the conserved phosphate 1 and 2 regions; the underlined dashed region refers' to the adenosine interaction region. Amino acids which are underlined with asterisks refer to the conserved sugar binding \\Mlb fil*s\hm.$\.Jntee\Kegp\"Ci\opecL 23429.97.doe 15/05/00 h domain. Sequence analysis was performed using the PILEUP/PRETTYBOX program set to standard parameters. Identical and similar residues are referred to as boxed and highlighted regions, respectively. Fig. IC is a schematic illustration showing the map positions of AtHXKJ and AtHXK2 on Arabidopsis chromosomes IV and II, respectively. Fig. 1D is a photograph of a DNA blot analysis showing that AtHXK is encoded by a multigene family. The blots were hybridized with a full-length cDNA probe ofAtHXKI (designated AtHXK, shown on the left) or AtHXK2 (designated AtHX2. shown on the right). Numbers indicated on the left of the blots refer to the molecular size markers in kilobases. Fig. IE is a photograph of a DNA blot analysis ofA. thaliana genomic DNA which was digested with HindIII, fractionated by gel electrophoresis, transferred to a nylon membrane, and hybridized with the AtHXKJ full-length cDNA probe under low stringency conditions. Fig. IF is an illustration showing the nucleotide sequence ofAtHXK1 (SEQ ID NO: Fig. IG is an illustration showing the nucleotide sequence of AtHXK2 (SEQ ID NO: 4).

Figs. 2A-B are a series of illustrations showing HXK expression in Arabidopsis. Fig. 2A is a photograph of an RNA blot showing the expression of .AtHXK1 and AtHXK2 in leaf (rosette and cauline), stem, flower, silique, and root tissues. Fig. 2B is a photograph of an RNA blot showing that the expression of AtHXKI and AtHXK2 is induced by light and sugar.

20 Figs. 3A-F are color photographs of Arabidopsis seedlings illustrating HXK as a sugar sensor in plants. Fig. 3A is a photograph of transgenic Arabidopsis seedlings which were germinated on 1/2 MS plates containing 6% glucose and which have increased expression of either sense-AtHXK1 (left) or anti-AtHXKI (middle) constructs. A wild-type (control) plant is shown on the right. Fig. 3B is a photograph se. 25 of transgenic Arabidopsis seedlings which were germinated on 1/2 MS plates containing 0.8mM 2-dGlc and which have increased expression of either sense- AtHXKJ (left) or anti-AtHXKI (middle) constructs. A wild-type (control) plant is "shown on the right. Fig. 3C is a photograph showing a T3 homozygous population of S sense-AtHXKl (left) and anti-AtHXK (right) plants which were germinated on 1/2 -11- MS plates containing 6% glucose. Fig. 3D is a photograph showing a T3 homozygous population of sense-AtHXK1 (left) and anti-AtHXKI (right) plants which were germinated on 1/2 MS plates containing 0.8mM 2-dGlc. Fig. 3E is a photograph showing sense-AtHXKI (left), anti-AtHXKJ (middle), and control (right) plants which were germinated on 1/2 MS plates containing 6% mannitol. Fig. 3F is a photograph showing sense-AtHXKI (left), anti-AtHXKI (middle), and control (right) plants which were germinated on 1/2 MS plates containing 6% 3-MeGlc.

Figs. 4A-C are a series of color photographs showing that AtHXK mediates sugar effects on seedling growth and development. Seedlings were grown in the dark for 6 days followed by illumination for 12 hours, on media containing various glucose concentrations (shown as increasing concentrations of glucose (Glc%) 2, 3, 4, 5, or Fig. 4A is a photograph showing that higher concentrations of glucose inhibit hypocotyl elongation and expansion as well as greening of cotyledons in wild-type (control) plants. Fig. 4B is a photograph of sense-AlHXKI plants that are hypersensitive to glucose as indicated by the strong inhibitory effects on seedling development. Fig. 4C is a photograph of anti-AtlXK1 plants that are less sensitive to glucose as shown by decreased inhibitory effects on seedling development when O compared to wild-type plants.

S* Figs. SA-F are a series of illustrations showing the expression of various 20 genes in control, sense-, and anti-sense plants. Fig. 5A is a photograph of an RNA blot analysis using illuminated etiolated seedlings which were germinated on 1/2 MS plates containing 6% glucose. UBQ expression was monitored as a control. Fig. 0 :2o is a photograph of an RNA blot analysis of RNA prepared from light-grown green plants (Light) which were propagated without exogenous sugars, and from light- 25 grown green plants (Dark) which were dark adapted for 3 days and then illuminated for 4 hours. Fig. SC is a photograph of several RNA blots showing the expression of sense and antisense constructs in the transgenic plants. RNAs were extracted from etiolated seedlings grown on 1/2 MS plates containing 6% glucose. Gene- and strandspecific probes were used to reveal sense-AtHXKl (sense-1), sense-AtHXK2 (sense-2), -12antisense-AtHXK1 (anti-l), and antisense-AtHXK2 (anti-2) transcripts. The blot that shows sense-AtHXK1 (sense-l) expression was exposed for a longer period of time than the other blots. Wild-type plants were used as controls. Fig. 5D is a photograph of a protein blot analysis showing the expression of AtHXK Sense-AtHXK plants showed elevated expression of AtHXK1, and anti-AtIHXK plants showed reduced expression. Wild-type plants were used as controls.

Fig. 5E is a bar graph showing the total hexose phosphorylation activities in etiolated seedlings. Fig. 5F is a bar graph showing the total hexose phosphorylation activities in light grown plants. Error bars show standard deviations.

Figs. 6A-C are a series of illustrations showing that sugar signaling is uncoupled from sugar metabolism. Shown in Fig. 6A are photographs demonstrating that the growth of the wild-type strain, but not the double mutant hxkl/hxk2, is inhibited on a 2-dGlc/raffinose plate (left). Increased expression of either AtHXK1 or AtHXK2 in the hxkl/hxk2 strain did not restore glucose repression, as shown by a level of growth for this strain on a 2-dGlc/raffinose plate which was similar to the double mutant transformed with vector (pFL61) alone (right). Fig. 6B is a color photograph showing the dominant interfering effect of increasing the expression yeast HXK2 in transgenic Arabidopsis seedlings YHXK2 plants) which were grown for 7 days on 1/2 MS plates containing 6% glucose. Fig. 6C is a bar graph showing total 20 hexose phosphorylation activities in etiolated or green YHXK2, sense-AtHXKl, and control plants. Error bars represent standard deviations.

There now follows a description of the cloning and characterization of two Arabidopsis HXK-encoding cDNAs which are useful in the instant invention, and a characterization of their ability to regulate sugar metabolism. These examples are S 25 provided for the purpose of illustrating the invention, and should not be construed as limiting.

-13- 0 P* Molecular Characterization ofArabidopsis HXK Genes To elucidate the role of HXK as a sugar sensor, the Arabidopsis HXK genes were cloned by functional complementation using a yeast Saccharomyces cerevisiae hxkl/hxk2 double mutant (designated DBY2219), a strain which lacked HXK activity (Ma and Botstein, Mol. Cell. Biol. 6, 4046 (1986)). Using this approach, we identified two cDNAs, designated AtHXK1 (Fig. IF; SEQ ID NO: 3, GenBank accession no. U28214) and AtHXK2 (Fig. 1G; SEQ ID NO: 4, GenBank accession no.

U28215). These cDNAs, which were 2.0 and 1.9 kb in length respectively, were both found reproducibly to complement the yeast double mutant and to allow its growth on a selection plate containing fructose as the sole carbon source. Exemplary results are shown in Fig. IA; mutant yeast cells transformed with either the AtHXK1 or AtHXK2 cDNAs were capable of growth on the selection media, indicating that these genes complemented the double mutant. In contrast, mutants transformed with the plasmid vector pFL61 alone were incapable of growth on the same selection media (Fig. 1 A) (Minet et al., Plant J. 2, 417 (1992)).

DNA sequence analyses of AtHXK1 (Fig. IF, SEQ ID NO: 3) and AtHXK2 (Fig. IF, SEQ ID NO: 4) predicted open reading frames of 496 and 502 amino acids, respectively (Fig. 1B). These genes were found to share 82% nucleotide identity and 85% amino acid identity. In addition, database searches and sequence comparisons 20 revealed that these AtHXKs shared between 34-3 5% sequence identity with the human and rat GLKs (Nishi et al., Diabetologia 35, 743 (1992); Magnuson et al., Proc. Natl.

Acad. Sci. U.S.A. 86, 4838 (1989)), and between 36-38% sequence identity with several yeast HXKs (Stachelek et al., Nucl. Acids Res. 14, 945 (1986); Prior et al., Mol. Cell. Biol. 13, 3882 (1993)). Conserved ATP- and sugar-binding domains were 25 also identified in the predicted amino acid sequences of both AtHXK genes. As shown in Fig. IB, three domains were identified which are involved in ATP binding (Bork et al., Protein Sci. 2, 31 (1993)). Also shown in Fig. 1B is a sugar binding domain which is similar to the glucose binding site found in mammalian GLK (Bork Set al., Protein Sci. 2, 31 (1993)). In general, our sequence comparison revealed that 14 ,1 -14the overall sequence and structure of the Arabidopsis HXKs were similar to those of the mammalian GLK and yeast HXKs, but distinct from that of plant fructokinase (Smith et al., Plant Physiol. 102, 1043 (1993)).

We next determined the chromosomal positions of AtHXK1 and AtHXK2 genes by standard segregation analysis of restriction fragment length polymorphisms (RFLPs) in recombinant inbred lines (Nam et al., Plant Cell 1, 699 (1989); Lister and Dean, Plant J. 4, 745 (1993); Hauge et al., Plant 3, 745 (1993); Schmidt et al., Science 270, 480 (1995); Zachgo et al., Genomic Res. 6, 19 (1996)). By this analysis, we found that AtHXKJ is located on chromosome 4 and is flanked by the chromosomal markers mi232 and g8300 (Fig. 1C), and that AtHXK2 is located on chromosome 2 and is flanked by the chromosomal markers mil48 and mi238 (Fig.

SC).

The copy number of the AtHXK genes was determined by genomic DNA (Southern) blot analysis. Genomic DNA was prepared according to standard methods from A. thaliana (Landsberg er), digested with BgllI, EcoRI, HindIII, or Xbal, fractionated by gel electrophoresis, transferred to a nylon membrane, and hybridized with a full-length cDNA randomly-primed probe of either AtHXK1 or AtHXK2 (Ausubel et al., infra). Genomic DNA blot analysis revealed that AtHXK1 hybridized at high stringency with two DNA fragments which corresponded to the two AtHXK 2. 0 genes (Fig. ID, blot designated AtHXKI). In addition, at least one other fragment was visible on the same blot when AtHXK2 was used as a probe under identical hybridization conditions (Fig. ID, blot designated AtHXK2). Using this same approach, a third cDNA (AtHXK3) was also identified, further supporting the hypothesis that three homologous HXK genes exist in Arabidopsis. At low stringency 25 conditions, a large number of additional bands were also detected, suggesting that more than three genes share sequence similarity with AtHXKJ (Fig. IE).

U

AtHXK Gene Expression To examine AtHXK gene expression, RNA blot experiments were performed as follows. RNA was extracted from rosette leaves, cauline leaves, stems, flowers, siliques, and roots according to standard methods. The extracted RNAs were gel fractionated and transferred to a nylon membrane (for example, as described in Ausubel et al., infra). Blots were subsequently hybridized with either AtHXKI, AtHXK2, or ubiquitin (UBQ) probes (Greenberg et al., Cell 77, 551 (1994)) according to standard techniques. The UBQ probe was used as a control in these experiments.

Equal amounts of RNA were loaded in each lane.

RNA blot analyses indicated that both AtHXKJ and AtHXK2 probes detected RNA bands of approximately 2 kb in length. As shown in Fig. 2A, the transcript levels of both AtHXKI and AtHXK2 were greatest in the siliques, moderate in flowers and rosette leaves, and lowest in the stem and cauline leaves. In roots, AtHXKI expression was greater than AtHXK2. The varied levels of AIHXKl and AtHXK2 expression may reflect their diverse physiological roles, for example, feedback regulation of photosynthesis in source tissues sugar providers) such as rosette leaves, and sugar metabolism in sink tissues sugar acceptors) such as siliques and flowers.

Since light is required for plants to produce sugars by photosynthesis, we 20 investigated the effect of light on AtHXK gene expression. RNA blot analyses were carried out as described above using total RNA prepared from dark-grown etiolated and light-grown dark-adapted wild-type plants, with or without illumination (designated in Fig. 2B as Dark and Light, respectively). In particular, dark-grown etiolated seedlings were germinated and grown on plates containing 1/2 Murashige- 2 5 Skoog (MS) medium, with or without 6% glucose (designated in Fig. 2B as +Sugar and -Sugar, respectively). Plants were grown in the dark for 6 days and then exposed S to white light (120 ItE m' 2 for 4 hours. Light-grown, dark-adapted plants consisted of fifteen-day-old light-grown green plants which were dark-adapted for 3 days and Sremained in the dark, or were illuminated and then flushed with 3% glucose -16- (designated in Fig. 2B as Light+Sugar). Growth conditions were as described by Cheng et al. (Proc. Natl. Acad. Sci., U.S.A. 89, 1861 (1992)).

As shown in Fig. 2B, both AtHXKI and AtHXK2 were found to be expressed at very low levels in non-photosynthetic etiolated seedlings, even after 4 hours of illumination. However, their expression was induced by the addition of exogenous sugar. The transcript levels of both AtHXKI and AtHXK2 were low in dark-adapted green plants, but was induced significantly upon illumination and further enhanced by sugar (Fig. 2B). UBQ gene expression was found to be affected by both light and sugar. These results revealed that AtHXK expression was tied to the conditions in o0 which sugar-sensing and metabolism were needed, indicating that plant sugar homeostasis was controlled by AtHXK levels through an autoregulatory mechanism.

AtHXK as a Sugar Sensor in Plants To test the hypothesis that AtHXKs act as sugar sensors in intact plants, transgenic plant models were established by introducing sense and antisense genes to alter AtHXK levels. Wild-type (Bensheim) Arabidopsis plants were transformed with binary vectors carrying gene fusions with the CaMV35S promoter and sense AtHXK1 (sense-AtHXKI), sense AtHXK2 (sense-AtHXK2), antisense AtHXK1 (anti-AtHXKl), or antisense AtHXK2 (anti-AtHXK2) using a standard Agrobacterium-mediated root :transformation protocol (Czako et al., Mol. Gen. Genet. 235, 33 (1992)). The 20 presence of a transgene was determined by NPTII expression and resultant kanamycin resistance, and by DNA blot analysis. Several transgenic lines of the T3 generation homozygous for the sense or antisense transgenes were selected for further analyses.

Sugar sensitivity of transgenic plants was examined by performing bioassays using 6% glucose or 0.8mM 2-deoxyglucose (2-dGlc), a nonmetabolizable glucose 25 analog. On 6% glucose plates, greening and expansion of cotyledons, initiation of true leaves, and elongation ofhypocotyl and root were suppressed in control (wildtype) Arabidopsis seedlings grown under constant light (Fig. 3A, right). These inhibitory effects caused by glucose were observed in six different Arabidopsis ecotypes including Bensheim C24, Columbia (Col), Landsberg erecta (Ler), -17- 4 I S.

RLD, and Wassilewskija (WS) (data not shown). In addition, the greening of cotyledons was found to be inhibited at a low concentration of 2-dGlc in control plants (Fig. 3B, right). This phenotype was consistent with the finding that 2-dGlc was capable of acting as a potent sugar signal that could trigger global repression of genes encoding photosynthetic proteins.

Compared to control plants, sense-AtHXK1 plants showed hypersensitivity to 6% glucose as indicated by stunted growth of the cotyledons, hypocotyl, and root (Fig. 3A, left). In contrast, anti-AtHXK1 plants turned green and elongated normally (Fig. 3A, middle), indicating that they were less sensitive to sugar. Fig. 3C illustrates that sugar hypersensitivity and insensitivity were displayed homogeneously in the T3 transgenic plant populations. As in the glucose assay, sense-AHXKI plants were hypersensitive to 2-dGlc as shown by the severe inhibition of greening of cotyledons (Fig. 3B, left; Fig. 3D, left). Anti-AtHXK plants were less sensitive to sugar and appeared green when germinated in the presence of 2-dGlc (Fig. 3B, middle; Fig. 3D, right).

As shown in Table 1 (below), similar phenotypes were observed in multiple independent transgenic lines generated with either sense or antisense AtHXK1 or AtHXK2. The scored phenotypes shown in Table 1 were determined based on the examination of light-grown, 7-day-old seedlings which were germinated on 1/2 MS plates containing either 6% glucose or 0.8mM of 2-dGlc. Sugar insensitive (Ins), S. hypersensitive (Hyp), and ambiguous phenotypes were scored and tabulated. The results of this analysis are presented in Table 1 (below).

Table 1 Sugar sensitivity in T3 homozygous transgenic plants.

25 6X glucose 0.8rM 2-dGlc Transgenes Total lines Ins Hyp A Ins Hyp A CaMV35S:sense-AtHXK1 13 0 11 2 0 13 0 CaNV35S:sense-AtHXK2 13 2* 8 3 1* 12 0 CanV35Santi-AtHXK1 14 9 3 2 13 0 1 CaMV35S:anti-AtHXK1 14 10 0 11 1 2 'Sugars insensitivity is believed to result from co-suppression.

-18- To rule out the possibility that the difference in sugar sensing between transgenic and control plants was due to an osmotic effect, mannitol and methylglucose (3-MeGlc) were used in control experiments. No apparent difference was observed between control and transgenic plants when plated on 6% mannitol (Fig. 3E) or 6% 3-MeGlc, a glucose analog which is not phosphorylated by HXK (Fig. 3F). Together, these results indicated that sugar sensing in transgenic plants was specific; because neither mannitol nor 3-MeGlc were able to replace glucose and interact with AtHXKs.

AtHXK Mediates Sugar Effects on Plant Growth and Development We next compared the effects of sugar on hypocotyl and cotyledon development in both wild-type and transgenic plants. For these experiments, Arabidopsis seedlings were grown on plates containing 2M6% glucose for six days in the dark. Since hypocotyl elongation occurs more in the dark, the inhibitory effect caused by sugar could be visually evaluated. Because light triggers cotyledon expansion and greening, these dark-grown seedlings were exposed to light for 12 hours to determine the effect of sugar on cotyledon development. Our results are shown in Figure 4.

In particular, in control plants, the hypocotyl length was inversely proportional to the glucose concentration (Fig. 4A). Under similar growth conditions, the sense- 20 AtHXK plants were hypersensitive to sugar as revealed by the reduction of hypocotyl length when grown in the presence of 3-6% glucose (Fig. 4B). In contrast, anti- AtHXK plants were able to elongate even in the presence of 5 or 6% glucose (Fig.

4C). Although glucose concentrations below 2% promoted seedling growth in the presence of other nutrients (data not shown), hypocotyl inhibition by glucose concentrations above 2% reflected sugar-sensing mediated through AtHXK.

S In contrast to light, glucose (at suppressed cotyledon greening and expansion in control plants (Fig. 4A). In sense-AtHXK plants, the impairment was greater as indicated by etiolated cotyledons (Fig. 4B). However, anti-AtHXK plants -19p were found to be less sensitive to all glucose concentrations and turned green normally (Fig. 4C). Sugar inhibition of cotyledon development is explained by the plant's ability to switch to heterotrophic growth in the presence of abundant external sugars rather than photoautotrophic growth for which cotyledon expansion and greening are required. We also observed that there was a lack of sugar inhibition in dark-grown roots of control and antisense seedlings (Fig. 4A and Fig. 4C). This could be the consequence of low AtHXK expression in roots in the dark because ectopic AtHXK expression conferred glucose-dependent inhibition of root growth in sense plants (Fig. 4B). These results indicated that distinct sugar responses could occur in different tissues due to differential expression of AtHXK (Fig. 2).

AtHXK Mediates Sugar Repression and Activation of Gene Expression To determine whether HXK was involved in sugar regulation of gene expression, we compared the expression levels of two sugar-repressible genes, the light-harvesting chlorophyll a/b binding protein (CAB1) and the ribulose bisphosphate carboxylase small subunit (RBCS), and one sugar-inducible gene, the nitrate reductase (NRI) gene in control, sense-, and anti-AtI-XK plants (Sheen, Photosynthesis Res. 39, 427 (1994); Thomas and Rodriguez, Plant Physiol. 106, 1235 (1994); Cheng et al., Proc. Natl. Acad. Sci. U.S.A. 89, 1861 (1992)).

We first examined illuminated dark-grown etiolated seedlings propagated on S* 20 6% glucose as described above. RNA blot analyses were performed using 1.1 kb CAB1, 0.5 kb RBCS, and 3.2 kb NRI probes from Arabidopsis; also as described above.

The transcription levels of CABI and RBCS were low in control plants, and nearly abolished in both sense-AtHXK1 and sense-AtHXK2 plants exhibiting sugar hypersensitivity (Fig. 5A). In contrast, both genes were expressed at high levels in both anti-AtHXK plants indicating sugar insensitivity. Consistent with the notion that sense transgenic plants are hypersensitive to sugars, NRI was activated in both sense- AtHXKJ and sense-AtHXK2 plants, but not in anti-AtHXK or control plants (Fig. Together, these data indicated that AtHXK was the sensor which mediated both sugarrepressible and sugar-inducible gene expression in higher plants. In addition, the transcription levels of CABI and RBCS were similar in sense-AIHXKs and control plants grown in the absence of sugars (data not shown), indicating that sugar sensing by the AtHXKs was specific, and that exogenous sugar was at least one signal used in illuminated etiolated seedlings.

To show that AtHXK regulated gene expression under physiological conditions, we examined CABI and RBCS expression in light-grown green plants without the addition of exogenous sugars (as described above). The results from these experiments showed that the transcript levels of both genes were nearly five-fold lower in sense-AtHXK plants than in anti-AtHXK or control plants (Fig. 5B). This differential expression was perhaps due to the repression of light inducibility by endogenous sugars mediated through the increased expression of AtHXK, because both genes showed uniformly low expression in the dark in transgenic and control plants (Fig. 5B) (data not shown for AtHXK2).

Altered AtHXK Expression in Transgenic Plants To confirm that the observed sugar hypersensitivity or insensitivity in transgenic plants correlated with transgene expression, RNA and protein blot analyses 20 were conducted as follows. RNA blot analyses were performed using gene- and .strand-specific probes for the sense and antisense constructs which were expressed in the transgenic plants. Probes were synthesized using a polymerase chain reaction (PCR) method described by Greenberg et al. (Cell 77, 551 (1994)). Oligonucleotides for use as PCR primers were designed from the sequence of AtHXK1 (SEQ ID NO: 3) and AtHXK2 (SEQ ID NO: and were used to amplify their respective cDNA fragments. The sense primers were 5'-ATGGGTAAAGTAGCTGTT-3'(SEQ ID NO: 10) and 5'-ATGGGTAAAGTGGCAGTTGCAA-3' (SEQ ID NO: 11) for AtHXK1 and AtHXK2, respectively. The antisense primers were -21- TTAAGAGTCTTCAAGGTAGAG-3' (SEQ ID NO: 12) and TTAACTTGTTTCAGAGTCATCTTC-3' (SEQ ID NO: 13) for AtHXK1 and AtHXK2, respectively. Plasmids (pBluescript M KS+) containing either AtHXKI or AtHXK2 full-length cDNAs were used as templates for the PCR reactions. RNAs were extracted from illuminated etiolated seedlings grown on 6% glucose plates, gel fractionated, blotted to nylon membranes, and hybridized with each probe as described above. In illuminated etiolated seedlings, the transcript levels of AtHXK1 (sense-1) in sense-AtHXK1 plants and AtHXK2 (sense-2) in sense-AtHXK2 plants were more than 20-fold higher than control plants (Fig. SC). In antisense plants, antisense RNAs of AtHXK1 (anti-1) and AtHXK2 (anti-2) were expressed in their respective antisense transgenic plants. In contrast, the endogenous transcript of AtHXKI in anti-AtHXKl and anti-AtHXK2 plants was reduced to less than 20% of the control level (Fig. 5C). Longer exposure of the sense-2 blot revealed that the endogenous AtHXK2 expression in anti-AtHXK1 and anti-AtHXK2 plants was also reduced (data not shown). These results indicated that either antisense AtHXK1 or antisense AtHXK2 RNA was capable of reducing the endogenous RNA levels of both AtHXKl and AtHXK2, presumably because of the high level of sequence identity.

Similar results were obtained when 15-day-old, light-grown green transgenic plants were analyzed (data not shown).

Protein blot analyses were also performed with seedlings which were germinated and grown in the dark for 6 days on plates containing 1/2 MS medium with or without 6% glucose, and then exposed to white light (120 gE m"s for 4 hours. These analyses were also performed using protein extracted from fifteen-dayold light-grown green plants which were dark adapted for 3 days and then illuminated for 4 hours. Antibodies which were used in these experiments were prepared as follows. AtHXK1 containing the entire open reading frame was subcloned into the plasmid vector pET-19b (Novagen) for overexpression in Escherichia coli according to standard methods. Overexpressed AtHXKI was then gel purified and used for the production of rabbit polyclonal antibodies. The antibodies were affinity purified, and -22- 9* 9 protein blot analyses were performed using the Phototope T M -Star Western Blot Detection Kit (New England Biolabs). Protein was extracted according to conventional methods (Wei et al., Cell 78, 1994; Tots et al. EMBO J. 6, 1843 (1987)).

The results of the protein blot experiments showed that AtHXKl expression was 5 to 10 fold higher in sense-AtHXKI than in control plants. In anti-AtHXKJ plants, the level of AtHXK1 was significantly lower than in control plants, although it was not completely eliminated (Fig. Hexose Phosphorvlation Activities in Transgenic Plants To determine whether the altered AtHXK expression affected the total catalytic activities of hexose phosphorylation in transgenic plants, we performed a series of standard hexose phosphorylation assays as described by Renz and Stitt (Planta 190, 166 (1993)).

In illuminated etiolated seedlings (grown as described above), sense-AtHXK1 plants were found to possess the highest hexose phosphorylation activity, whereas other plants displayed lower activities (Fig. 5E). The higher activity detected in plants having increased expression of the AtHXK gene was consistent with the result of a yeast transformation experiment indicating that AtHXK1 had higher catalytic activity than AtHXK2 (data not shown).

We also carried out the enzymatic assay using fifteen-day-old, light-grown 20 green plants that were dark-adapted for 3 days and illuminated for 4 hours. As shown in Fig. 5F, both sense-AtHXKl and sense-AtHXK2 plants had higher hexose phosphorylation activities than anti-AtHXK and control plants. Together, these data provided evidence for the conclusion that the manipulation of AtHXK expression is sufficient to alter sugar-sensing and sugar-regulated activities in Arabidopsis.

25 Therefore, the specific interaction between sugars and HXK, for example, AtHXKI and AtHXK2, but not the total catalytic activity of HXK, was shown to be a key determinant of sugar-sensing mechanisms in plants.

-23- 3 -23- V V Sugar Signaling is Uncoupled from Sugar Metabolism in Plants The above observations suggested the existence of a regulatory function for HXK, and the uncoupling of sugar signaling from metabolism in plants. To confirm this hypothesis, we sought to increase the expression of a heterologous HXK that would provide excess catalytic activity for sugar metabolism, but no regulatory function. The yeast HXK2 (YHXK2) has been proposed to have catalytic and regulatory functions, and appeared to be a good candidate for this experiment (Entian, Mol. Gen. Genet. 178, 633 (1980); Entian and FrShlich, J. Bacteriol. 158, 29 (1984); Entian et al., Mol. Cell. Biol. 5, 3035 (1985)). We first determined whether the putative regulatory functions of the YHXK2 and AtHXK were interchangeable by examining the effect of increasing the expression of AtHXK on glucose repression in a yeast hxkl/hxk2 double mutant (DBY2219). The assay was based on the YHXK2mediated growth inhibition glucose repression) of wild-type yeast cells on a 2dGlc/raffinose plate. The glucose repression assay was performed using a YP plate with 2% raffinose as the carbon source in the presence of 2-deoxyglucose as described by Ma et al. (Mol. Cell. Biol. 9, 5643 (1989)). The glucose analog, 2-dGlc, mimics glucose by inducing strong repression of the invertase gene (SUC2), but is itself unavailable for use as a carbon source. Thus, wild-type yeast strains exhibit glucose repression and cannot grow under these assay conditions; in contrast, in the 20 hxkl/hxk2 double mutant, SUC2 expression is derepressed, allowing raffinose hydrolysis and the release of fructose for growth on assay plates. As shown in Fig.

6A, DBY2219 grew on a 2-dGlc/raffinose plate due to the lack of YHXK2 and derepression of invertase gene expression. However, growth of this strain was inhibited upon transformation with YHXK2 and restoration of glucose repression (Fig. 6A) (Ma and Botstein, Mol. Cell. Biol. 6, 4046 (1986); Ma et al., Mol. Cell. Biol.

9, 5643 (1989)).

To determine the effect of increasing the expression of YHXK2 in plants, a transgene construct, pCaMV35S-YHXK2, that expressed YHXK2 was introduced into -24- Arabidopsis using the Agrobacterium-mediated protocol described above. Transgenic plants having increased expression of YHXK2 (YHXK2 plants) were observed to display sugar insensitivity in many assays. For instance, YHXK2 seedlings were less sensitive to 6% glucose than control and sense-AtHXK plants. Hypocotyl elongation, root growth, and greening of cotyledons were found to be inhibited in sense-AtHXK1 or control plants, but not in YHXK2 plants (Fig. 6B). RNA blot analysis showed that CAB1 and RBCS transcripts were not repressed in YHXK2 plants, whether grown with or without exogenous glucose (data not shown).

To insure that YHXK2 provided hexose phosphorylation activity in plants, enzymatic assays were conducted using both etiolated and green transgenic plants.

Fig. 6C shows that total hexose phosphorylation activity was much higher in YHXK2 than in control plants, and similar to or higher than sense-AtHXK plants. However, YHXK2 plants were sugar-insensitive rather than hypersensitive (Fig. 6B). This dominant interfering effect of YHXK2 in transgenic plants presumably resulted from the increased expression of YHXK2 which competed with AtHXK for sugars, but which was incapable of transmitting a signal. We ruled out the possibility of gene silencing effects based on the normal expression of AtHXKI and ATHXK2 in YHXK2 plants (data not shown).

These experiments indicated that the catalytic function of HXK was 20 interchangeable between yeast and plants, but not the regulatory function for sugarsignaling. Our recent results have also shown that a third AtHXK does not complement HXK regulatory function (data not shown). Thus, glucose-signaling does not require extensive metabolism and is diminished when YHXK2 is overexpressed in plants.

In sum, we have found that HXK mediates sugar-sensing in higher plants based on the analyses of transgenic plants with gain or loss of AtHXK function, and a dominant interfering YHXK2.

Isolation of Other HXK cDNAs and Genomic DNAs Based on the isolation described herein of the aforementioned HXK genes and polypeptides, the isolation of additional plant HXK coding sequences is made possible using standard strategies and techniques that are well known in the art. For example, using all or a portion of the amino acid sequence of an HXK polypeptide, one may readily design HXK-specific oligonucleotide probes, including HXK degenerate oligonucleotide probes a mixture of all possible coding sequences for a given amino acid sequence). These oligonucleotides may be based upon the sequence of either DNA strand and any appropriate portion of the HXK sequence (for example, Fig. 1F-G; SEQ ID NOS: 3 and 4, respectively). General methods for designing and preparing such probes are provided, for example, in Ausubel et al., 1996, Current Protocols in Molecular Biology, Wiley Interscience, New York, and Berger and Kimmel, Guide to Molecular Cloning Techniques, 1987, Academic Press, New York. These oligonucleotides are useful for HXK gene isolation, either through their use as probes capable of hybridizing to HXK complementary sequences or as primers for various amplification techniques, for example, polymerase chain reaction (PCR) cloning strategies.

Hybridization techniques and screening procedures are well known to those skilled in the art and are described, for example, in Ausubel et al. (supra); Berger and Kimmel (supra); and Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press, New York. If desired, a combination of different oligonucleotide probes may be used for the screening of a recombinant DNA library. The oligonucleotides may be detectably-labeled using methods known in the art and used to probe filter replicas from a recombinant DNA library. Recombinant DNA libraries are prepared according to methods well known in the art, for example, as described in Ausubel et al. (supra), or they may be obtained from commercial i sources.

For detection or isolation of closely related HXK sequences having greater than 80% identity, high stringency conditions are preferably used; such conditions -26include hybridization at about 65 C and about 50% formamide, a first wash at about about 2X SSC, and 1% SDS, followed by a second wash at about 65 0 C and about 0.1% SDS, and IX SSC. Lower stringency conditions for detecting HXK genes having about 30-50% sequence identity to the HXK genes described herein include, for example, hybridization at about 45 C in the absence of formamide, a first wash at about 45 C, about 6X SSC, and about 1% SDS, and a second wash at about about 6X SSC, and about 1% SDS. These stringency conditions are exemplary; other appropriate conditions may be determined by those skilled in the art.

As discussed above, HXK oligonucleotides may also be used as primers in amplification cloning strategies, for example, using PCR. PCR methods are well known in the art and are described, for example, in PCR Technology, Erlich, ed., Stockton Press, London, 1989; PCR Protocols: A Guide to Methods and Applications, Innis et al., eds., Academic Press, Inc., New York, 1990; and Ausubel et al. (supra).

Primers are optionally designed to allow cloning of the amplified product into a suitable vector, for example, by including appropriate restriction sites at the 5' and 3' ends of the amplified fragment (as described herein). If desired, HXK may be isolated using the PCR "RACE" technique, or Rapid Amplification ofcDNA Ends (see, e.g., Innis et al. (supra)). By this method, oligonucleotide primers based on an HXK .sequence are oriented in the 3' and 5' directions and are used to generate overlapping 20 PCR fragments. These overlapping and 5'-end RACE products are combined to produce an intact full-length cDNA. This method is described in Innis et al. (supra); and Frohman et al., Proc. Natl. Acad. Sci. USA 85, 8998, (1988).

Alternatively, any plant cDNA expression library may be screened by functional complementation of a yeast hxkl/hxk2 double mutant as described herein by Ma and Botstein Mol. Cell. Biol. 6, 4046 (1986)).

Useful HXK sequences may be isolated from any appropriate organism.

Confirmation of a sequence's relatedness to the HXK polypeptide family may be accomplished by a variety of conventional methods including, but not limited to, functional complementation assays and sequence comparison. In addition, the activity of any HXK sequence may be evaluated according to any of the techniques described herein.

Polypeptide Expression HXK polypeptides may be produced by transformation of a suitable host cell with all or part of an HXK cDNA (for example, the cDNA described above) in a suitable expression vehicle or with a plasmid construct engineered for increasing the expression of an HXK polypeptide (supra) in vivo.

Those skilled in the field of molecular biology will understand that any of a wide variety of expression systems may be used to provide the recombinant protein.

The precise host cell used is not critical to the invention. The HXK protein may be produced in a prokaryotic host, for example, E. coli, or in a eukaryotic host, for example, Saccharomyces cerevisiae, mammalian cells (for example, COS 1 or NIH 3T3 cells), or any of a number of plant cells including, without limitation, algae, tree species, ornamental species, temperate fruit species, tropical fruit species, vegetable species, legume species, monocots, dicots, or in any plant of commercial or agricultural significance. Particular examples of suitable plant hosts include, but are not limited to, Conifers, Petunia, Tomato, Potato, Tobacco, Arabidopsis, Lettuce, Sunflower, Oilseed rape, Flax, Cotton, Sugarbeet, Celery, Soybean, Alfalfa, Medicago, Lotus, Vigna, Cucumber, Carrot, Eggplant, 20 Cauliflower, Horseradish, Morning Glory, Poplar, Walnut, Apple, Asparagus, Rice, Maize, Millet, Onion, Barley, Orchard grass, Oat, Rye, and Wheat.

Such cells are available from a wide range of sources including: the American Type Culture Collection (Rockland, MD); or from any of a number seed companies, for example, W. Atlee Burpee Seed Co. (Warminster, PA), Park Seed Co.

(Greenwood, SC), Johnny Seed Co. (Albion, ME), or Northrup King Seeds 6. (Harstville, SC). Descriptions and sources of useful host cells are also found in Vasil Cell Culture and Somatic Cell Genetics of Plants, Vol I, II, III Laboratory Procedures and Their Applications Academic Press, New York, 1984; Dixon, R.A., -28-

I*

Plant Cell Culture-A Practical Approach, IRL Press, Oxford University, 1985; Green et al., Plant Tissue and Cell Culture, Academic Press, New York, 1987; and Gasser and Fraley, Science 244, 1293, (1989).

For prokaryotic expression, DNA encoding an HXK polypeptide is carried on a vector operably linked to control signals capable of effecting expression in the prokaryotic host. If desired, the coding sequence may contain, at its 5' end, a sequence encoding any of the known signal sequences capable of effecting secretion of the expressed protein into the periplasmic space of the host cell, thereby facilitating recovery of the protein and subsequent purification. Prokaryotes most frequently used are various strains of E. coli; however, other microbial strains may also be used.

Plasmid vectors are used which contain replication origins, selectable markers, and control sequences derived from a species compatible with the microbial host.

Examples of such vectors are found in Pouwels et al. (supra) or Ausubel et al.

(supra). Commonly used prokaryotic control sequences (also referred to as "regulatory elements") are defined herein to include promoters for transcription initiation, optionally with an operator, along with ribosome binding site sequences.

Promoters commonly used to direct protein expression include the beta-lactamase (penicillinase), the lactose (lac) (Chang et al., Nature 198, 1056 (1977)), the tryptophan (Trp) (Goeddel et al., Nucl. Acids Res. 8, 4057 (1980)), and the tac 20 promoter systems, as well as the lambda-derived PL promoter and N-gene ribosome binding site (Simatake et al., Nature 292, 128 (1981)).

One particular bacterial expression system for HXK polypeptide production is the E. coli pET expression system (Novagen, Inc., Madison, WI). According to this expression system, DNA encoding an HXK polypeptide is inserted into a pET vector in an orientation designed to allow expression. Since the HXK gene is under the control of the T7 regulatory signals, expression of HXK is induced by inducing the i expression ofT7 RNA polymerase in the host cell. This is typically achieved using host strains which express T7 RNA polymerase in response to IPTG induction. Once -29- 4* 4* produced, recombinant HXK polypeptide is then isolated according to standard methods known in the art, for example, those described herein.

Another bacterial expression system for HXK polypeptide production is the pGEX expression system (Pharmacia). This system employs a GST gene fusion system which is designed for high-level expression of genes or gene fragments as fusion proteins with rapid purification and recovery of functional gene products. The protein of interest is fused to the carboxyl terminus of the glutathione S-transferase protein from Schistosomajaponicum and is readily purified from bacterial lysates by affinity chromatography using Glutathione Sepharose 4B. Fusion proteins can be recovered under mild conditions by elution with glutathione. Cleavage of the glutathione S-transferase domain from the fusion protein is facilitated by the presence of recognition sites for site-specific proteases upstream of this domain. For example, proteins expressed in pGEX-2T plasmids may be cleaved with thrombin; those expressed in pGEX-3X may be cleaved with factor Xa.

For eukaryotic expression, the method of transformation or transfection and the choice of vehicle for expression of the HXK polypeptide will depend on the host system selected. Transformation and transfection methods are described, in Ausubel et al. (supra); Weissbach and Weissbach, Methods for Plant Molecular Biology, Academic Press, 1989; Gelvin et al., Plant Molecular Biology Manual, 20 Kluwer Academic Publishers, 1990; Kindle, K, Proc. Nail. Acad. Sci.. U.S.A 87, 1228 (1990); Potrykus, Annu. Rev. Plant Physiol. Plant Mol. Biology 42, 205 (1991); and BioRad (Hercules, CA) Technical Bulletin #1687 (Biolistic Particle Delivery Systems). Expression vehicles may be chosen from those provided, in Cloning Vectors: A Laboratory Manual Pouwels et al., 1985, Supp. 1987); Gasser and Fraley (S1ura); Clontech Molecular Biology Catalog (Catalog 1992/93 Tools for the Molecular Biologist, Palo Alto, CA); and the references cited above.

One preferred eukaryotic expression system is the mouse 3T3 fibroblast host cell transfected with a pMAMneo expression vector (Clontech). pMAMneo provides: .RSV-LTR enhancer linked to a dexamethasone-inducib MTV-LTR promotor, an RSV-LTR enhancer linked to a dexamethasone-inducible MMTV-LTR promotor, an SV40 origin of replication which allows replication in mammalian systems, a selectable neomycin gene, and SV40 splicing and polyadenylation sites. DNA encoding an HXK polypeptide is inserted into the pAMneo vector in an orientation designed to allow expression. The recombinant HXK. protein is then isolated as described below. Other preferable host cells which may be used in conjunction with the pMAMneo expression vehicle include COS cells and CHO cells (ATCC Accession Nos. CRL 1650 and CCL 61, respectively).

Alternatively, if desired, an HXK polypeptide is produced by a stablytransfected mammalian cell line. A number of vectors suitable for stable transfection of mammalian cells are available to the public, see Pouwels et al. (supra); methods for constructing such cell lines are also publicly available, in Ausubel et al. (supra). In one example, cDNA encoding the HXK polypeptide is cloned into an expression vector which includes the dihydrofolate reductase (DHFR) gene.

Integration of the plasmid and, therefore, the HXK-encoding gene into the host cell chromosome is selected for by inclusion of 0.01-300 .zM methotrexate in the cell culture medium (as described in Ausubel et al., supra). This dominant selection can be accomplished in most cell types. Recombinant protein expression can be increased by DHFR-mediated amplification of the transfected gene. Methods for selecting cell lines bearing gene amplifications are described in Ausubel et al. (supra); such 20 methods generally involve extended culture in medium containing gradually increasing levels of methotrexate. DHFR-containing expression vectors commonly used for this purpose include pCVSEII-DHrF and pAdD26SV(A) (described in Ausubel et al., supra). Any of the host cells described above or, preferably, a DHFRdeficient CHO cell line (for example, CHO DHFR cells, ATCC Accession No. CRL 9096) are among the host cells preferred for DHFR selection of a stably-transfected cell line or DHFR-mediated gene amplification.

i Most preferably, an HXK polypeptide is produced by a stably-transfected plant cell line or by a transgenic plant. A number of vectors suitable for stable transfection of plant cells or for the establishment of transgenic plants are available to 0 o~o -31-

C

r the public; such vectors are described in Pouwels et al. (supra), Weissbach and Weissbach (supra), and Gelvin et al. (supra). Methods for constructing such cell lines are described in, Weissbach and Weissbach (supra), and Gelvin et al. (supra).

Typically, plant expression vectors include a cloned plant gene under the transcriptional control of 5' and 3' regulatory sequences and a dominant selectable marker. Such plant expression vectors may also contain, if desired, a promoter regulatory region (for example, one conferring inducible or constitutive, environmentally- or developmentally-regulated, or cell- or tissue-specific expression), a transcription initiation start site, a ribosome binding site, an RNA processing signal, a transcription termination site, and/or a polyadenylation signal.

Alternatively, the HXK polypeptide may be produced using a transient expression system the maize transient expression system described by Sheen Plant Cell 2, 1027 (1990)).

Once the desired HXK nucleic acid sequences is obtained it may be manipulated in a variety of ways known in the art. For example, where the sequence involves noncoding flanking regions, the flanking regions may be subjected to mutagenesis.

The HXK DNA sequence of the invention may, if desired, be combined with other DNA sequences in a variety of ways. The HXK DNA sequence of the invention may be employed with all or part of the gene sequences normally associated with the HXK protein. In its component parts, a DNA sequence encoding an HXK protein is combined in a DNA construct having a transcription initiation control region capable of promoting transcription and translation in a host cell.

In general, the constructs will involve regulatory regions functional in plants which provide for modified production of HXK protein as discussed herein. The open S reading frame coding for the HXK protein or functional fragment thereof will be joined at its 5' end to a transcription initiation regulatory region such as the sequence naturally found in the 5' upstream region of the HXK structural gene. Numerous other -32transcription initiation regions are available which provide for constitutive or inducible regulation.

For applications when developmental, cell, tissue, hormonal, or environmental expression is desired, appropriate 5' upstream non-coding regions are obtained from other genes; for example, from genes regulated during seed development, embryo development, or leaf development.

Regulatory transcript termination regions may also be provided in DNA constructs of this invention as well. Transcript termination regions may be provided by the DNA sequence encoding the HXK protein or any convenient transcription termination region derived from a different gene source. The transcript termination region will contain preferably at least 1-3 kb of sequence 3' to the structural gene from which the termination region is derived. Plant expression constructs having HXK as the DNA sequence of interest for expression (in either the sense or antisense orientation) thereof may be employed with a wide variety of plant life, particularly plant life involved in the production of storage reserves (for example, those involving carbon and nitrogen metabolism). Such genetically-engineered plants are useful for a variety of industrial and agricultural applications as discussed below. Importantly, this invention is applicable to dicotyledons and monocotyledons, and will be readily applicable to any new or improved transformation or regeneration method.

An example of a useful plant promoter according to the invention is a caulimovirus promoter, for example, a cauliflower mosaic virus (CaMV) promoter.

These promoters confer high levels of expression in most plant tissues, and the activity of these promoters is not dependent on virally encoded proteins. CaMV is a source for both the 35S and 19S promoters. In most tissues oftransgenic plants, the CaMV 35S promoter is a strong promoter (see, Odell et al., Nature 313, 810 (1985)). The CaMV promoter is also highly active in monocots (see, Dekeyser et al., Plant Cell 2, 591 (1990); Terada and Shimamoto, Mol. Gen. Genet. 220, 389, (1990)). Moreover, activity of this promoter can be further increased between 2- 10 fold) by duplication of the CaMV 35S promoter (see Kay et al., Science 236, -33- 1299 (1987); Ow et al., Proc. Natl. Acad. Sci., U.S.A. 84,4870 (1987); and Fang et al., Plant Cell 1, 141 (1989)).

Other useful plant promoters include, without limitation, the nopaline synthase promoter (An et al., Plant Physiol. 88, 547 (1988)) and the octopine synthase promoter (Fromm et al., Plant Cell 1, 977 (1989)).

For certain applications, it may be desirable to produce the HXK gene product in an appropriate tissue, at an appropriate level, or at an appropriate developmental time. For this purpose, there are an assortment of gene promoters, each with its own distinct characteristics embodied in its regulatory sequences, shown to be regulated in response to the environment, hormones, and/or developmental cues. These include gene promoters that are responsible for heat-regulated gene expression (see, e.g., Callis et al., Plant Physiol. 88, 965 (1988); Takahashi and Komeda, Mol. Gen. Genet.

219, 365 (1989); and Takahashi et al. Plant J. 2, 751 (1992)), light-regulated gene expression the pea rbcS-3A described by Kuhlemeier et al., Plant Cell 1, 471 (1989); the maize rbcS promoter described by Schlffner and Sheen, Plant Cell 3, 997 (1991); or the cholorphyll a/b-binding protein gene found in pea described by Simpson et al., EMBO J. 4, 2723 (1985)), hormone-regulated gene expression (for example, the abscisic acid (ABA) responsive sequences from the Em gene of wheat Sdescribed by Marcotte et al., Plant Cell 1, 969 (1989); the ABA-inducible HVAl and HVA22, and rd29A promoters described for barley and Arabidopsis by Straub et al., Plant Cell 6, 617 (1994), Shen et al., Plant Cell 7, 295 (1994), and Yamaguchi- Shinosaki et al wound-induced gene expression (for example, of wunl described by Siebertz et al., Plant Cell 1, 961 (1989)), or organ-specific gene expression (for example, of the tuber-specific storage protein gene described by Roshal et al., EMBO 25 J. 6, 1155 (1987); the 23-kDa zein gene from maize described by Schemthaner et al., EMBO J. 7, 1249 (1988); or the French bean 8-phaseolin gene described by Bustos et al., Plant Cell 1, 839 (1989)).

Plant expression vectors may also optionally include RNA processing signals, e.g, introns, which have been shown to be important for efficient RNA synthesis and e.g, introns, which have been shown to be important for efficient RNA synthesis and -34f accumulation (Callis et al., Genes and Dev. 1, 1183 (1987)). The location of the RNA splice sequences can dramatically influence the level of transgene expression in plants. In view of this fact, an intron may be positioned upstream or downstream of an HXK polypeptide-encoding sequence in the transgene to modulate levels of gene expression.

In addition to the aforementioned 5' regulatory control sequences, the expression vectors may also include regulatory control regions which are generally present in the 3' regions of plant genes (Thornburg et al., Proc. Natl. Acad. Sci. U.S.A.

84, 744 (1987); An et al., Plant Cell 1, 115 (1989)). For example, the 3' terminator region may be included in the expression vector to increase stability of the mRNA.

One such terminator region may be derived from the PI-II terminator region of potato.

In addition, other commonly used terminators are derived from the octopine or nopaline synthase signals.

The plant expression vector also typically contains a dominant selectable marker gene used to identify those cells that have become transformed. Useful selectable genes for plant systems include genes encoding antibiotic resistance genes, for example, those encoding resistance to hygromycin, kanamycin, bleomycin, G418, streptomycin or spectinomycin. Genes required for photosynthesis may also be used S as selectable markers in photosynthetic-deficient strains. Alternatively, the green- S. 20 fluorescent protein from the jellyfish Aequorea victoria may be used as a selectable marker (Sheen et al., Plant J. 8:777, 1995; Chiu et al., Current Biology 6, 325 (1996)). Finally, genes encoding herbicide resistance may be used as selectable markers; useful herbicide resistance genes include the bar gene encoding the enzyme phosphinothricin acetyltransferase and conferring resistance to the broad spectrum herbicide Basta® (Hoechst AG, Frankfurt, Germany).

Efficient use of selectable markers is facilitated by a determination of the susceptibility of a plant cell to a particular selectable agent and a determination of the concentration of this agent which effectively kills most, if not all, of the transformed cells. Some useful concentrations of antibiotics for tobacco transformation include, e 75-100 gg/ml (kanamycin), 20-50 tg/ml (hygromycin), or 5-10 tg/ml (bleomycin). A useful strategy for selection oftransformants for herbicide resistance is described, by Vasil et al., supra.

It should be readily apparent to one skilled in the art of molecular biology, especially in the field of plant molecular biology, that the level of gene expression is dependent, not only on the combination of promoters, RNA processing signals, and terminator elements, but also on how these elements are used to increase the levels of selectable marker gene expression.

Plant Transformation Upon construction of the plant expression vector, several standard methods are available for introduction of the vector into a plant host, thereby generation a transgenic plant. These methods include Agrobacterium-mediated transformation tumefaciens or A. rhizogenes) (see, Lichtenstein and Fuller In: Genetic Engineering, vol 6, PWJ Rigby, ed, London, Academic Press, 1987; and Lichtenstein, and Draper, In: DNA Cloning, Vol II, D.M. Glover, ed, Oxford, IRI Press, 1985)), the particle delivery system (see, Gordon-Kamm et al., Plant Cell 2, 603 (1990); or BioRad Technical Bulletin 1687, supra), microinjection protocols (see, Green et al., supra), polyethylene glycol (PEG) procedures (see, e.g., Draper et al., Plant Cell Physiol. 23, 451 (1982); or Zhang and Wu, Theor. Appl.

Genet. 76, 835 (1988)), liposome-mediated DNA uptake (see, Freeman et al., Plant Cell Physiol. 25, 1353 (1984)), electroporation protocols (see, Gelvin et al., supra; Dekeyser et al., supra; Fromm et al., Nature 319,791 (1986); Sheen Plant Cell 2, 1027 (1990);or Jang and Sheen Plant Cell 6, 1665 (1994)), and the vortexing method (see, Kindle supra). The method of transformation is not critical to the instant invention. Any method which provides for efficient transformation may be employed. As newer methods are available to transform crops or other host cells, they may be directly applied.

-36- The following is an example outlining one particular technique, an Agrobacterium-mediated plant transformation. By this technique, the general process for manipulating genes to be transferred into the genome of plant cells is carried out in two phases. First, cloning and DNA modification steps are carried out in E. coli, and the plasmid containing the gene construct of interest is transferred by conjugation or electroporation into Agrobacterium. Second, the resulting Agrobacterium strain is used to transform plant cells. Thus, for the generalized plant expression vector, the plasmid contains an origin of replication that allows it to replicate in Agrobacterium and a high copy number origin of replication functional in E. coli. This permits facile production and testing of transgenes in E. coli prior to transfer to Agrobacterium for subsequent introduction into plants. Resistance genes can be carried on the vector, one for selection in bacteria, for example, streptomycin, and another that will function in plants, for example, a gene encoding kanamycin resistance or herbicide resistance.

Also present on the vector are restriction endonuclease sites for the addition of one or more transgenes and directional T-DNA border sequences which, when recognized by the transfer functions of Agrobacterium, delimit the DNA region that will be transferred to the plant.

In another example, plant cells may be transformed by shooting into the cell tungsten microprojectiles on which cloned DNA is precipitated. In the Biolistic 20 Apparatus (Bio-Rad) used for the shooting, a gunpowder charge (22 caliber Power Piston Tool Charge) or an air-driven blast drives a plastic macroprojectile through a gun barrel. An aliquot of a suspension of tungsten particles on which DNA has been SC' "precipitated is placed on the front of the plastic macroprojectile. The latter is fired at an acrylic stopping plate that has a hole through it that is too small for the macroprojectile to pass through. As a result, the plastic macroprojectile smashes against the stopping plate, and the tungsten microprojectiles continue toward their target through the hole in the plate. For the instant invention the target can be any plant cell, tissue, seed, or embryo. The DNA introduced into the cell on the microprojectiles becomes integrated into either the nucleus or the chloroplast.

-37- 0 In general, transfer and expression of transgenes in plant cells are now routine practices to those skilled in the art, and have become major tools to carry out gene expression studies in plants and to produce improved plant varieties of agricultural or commercial interest.

Transgenic Plant Regeneration Plants cells transformed with a plant expression vector can be regenerated, for example, from single cells, callus tissue, or leaf discs according to standard plant tissue culture techniques. It is well known in the art that various cells, tissues, and organs from almost any plant can be successfully cultured to regenerate an entire plant; such techniques are described, in Vasil supra; Green et al., supra; Weissbach and Weissbach, supra; and Gelvin et al., supra.

In one particular example, a cloned HXK polypeptide or an antisense construct under the control of the 35S CaMV promoter and the nopaline synthase terminator and carrying a selectable marker (for example, kanamycin resistance) is transformed into Agrobacterium. Transformation of leaf discs (for example, of tobacco leaf discs), with vector-containing Agrobacterium is carried out as described by Horsch et al.

(Science 227, 1229 (1985)). Putative transfonnants are selected after a few weeks (for :example, 3 to 5 weeks) on plant tissue culture media containing kanamycin 100 Sg/ml). Kanamycin-resistant shoots are then placed on plant tissue culture media without hormones for root initiation. Kanamycin-resistant plants are then selected for greenhouse growth. If desired, seeds from self-fertilized transgenic plants can then be sowed in a soil-less medium and grown in a greenhouse. Kanamycin-resistant progeny are selected by sowing surfaced sterilized seeds on hormone-free kanamycincontaining media. Analysis for the integration of the transgene is accomplished by standard techniques (see, for example, Ausubel et al. supra; Gelvin et al. supra).

Transgenic plants expressing the selectable marker are then screened for transmission of the transgene DNA by standard immunoblot and DNA detection techniques. Each positive transgenic plant and its transgenic progeny are unique in -38comparison to other transgenic plants established with the same transgene.

Integration of the transgene DNA into the plant genomic DNA is in most cases random, and the site of integration can profoundly effect the levels and the tissue and developmental patterns of transgene expression. Consequently, a number of transgenic lines are usually screened for each transgene to identify and select plants with the most appropriate expression profiles.

Transgenic lines are evaluated on levels of transgene expression. Expression at the RNA level is determined initially to identify and quantitate expression-positive plants. Standard techniques for RNA analysis are employed and include PCR amplification assays using oligonucleotide primers designed to amplify only transgene RNA templates and solution hybridization assays using transgene-specific probes (see, Ausubel et al., supra). The RNA-positive plants are then analyzed for protein expression by Western immunoblot analysis using HXK specific antibodies (see, Ausubel et al., supra). In addition, in situ hybridization and immunocytochemistry according to standard protocols can be done using transgenespecific nucleotide probes and antibodies, respectively, to localize sites of expression within transgenic tissue.

Once the recombinant HXK protein is expressed in any cell or in a transgenic plant (for example, as described above), it may be isolated, using affinity chromatography. In one example, an anti-HXK antibody produced as described in Ausubel et al., supra, or by any standard technique) may be attached to a column and used to isolate the polypeptide. Lysis and fractionation of HXK-producing cells *prior to affinity chromatography may be performed by standard methods (see, e.g., Ausubel et al., supra). Once isolated, the recombinant protein can, if desired, be 25 further purified, for example, by high performance liquid chromatography (see, e.g., Fisher, Laboratory Techniques In Biochemistry And Molecular Biology, eds., Work and Burdon, Elsevier, 1980).

These general techniques of polypeptide expression and purification can also be used to produce and isolate useful HXK fragments or analogs.

-39- Use The invention described herein is useful for a variety of agricultural and commercial purposes including, but not limited to, increasing crop yields, improving crop and ornamental quality, and reducing agricultural production costs. For example, the methods, DNA constructs, proteins, and transgenic plants described herein are useful for improving fruit and vegetable characteristics including: taste, texture, size, color, acidity or sweetness; nutritional content; disease resistance; and ripening processes.

Our results presented above demonstrate that it is possible to modulate hexokinase gene expression in transgenic plants by providing for the transcription of a hexokinase sequence that is complementary to the mRNA of an endogenous plant hexokinase. In this manner, various plant processes can be modified, controlled, or manipulated, resulting in enhancement of production of carbohydrate sucrose and starch) products, changes in plant growth, cellular differentiation and development, changes in plant phenotypes, and alteration of carbon/nitrogen partitioning and accumulation. In addition, as is discussed above, antisense expression can be controlled, if desired, in a cell-, tissue-, organ-, or developmentallyspecific manner. Thus, the use of antisense control can provide for substantial inhibition or varying degrees of reduction of hexokinase gene expression. In this 20 manner, cellular phenotypes can be modified without the production of extraneous proteins and with particular targeting to a specific gene.

For example, transgenic plants expressing antisense hexokinase RNA constructs are useful for eliminating feedback inhibition of photosynthesis (for example, by sugar induced repression of photosynthetic genes) that is caused by the accumulation of sugar metabolites (for example, the photosynthetic endproducts sucrose and glucose). As shown herein, transgenic plants expressing antisense hexokinase genes are less sensitive to sugar, and are no longer subject to growth limitations and restrictions that are the result of sugar repression (for example, reduction of photosynthetic gene expression). In particular, we have discovered that transgenic plants expressing antisense hexokinase genes develop normally and thrive under conditions that typically limit and restrict plant growth due to feedback inhibition (for example, in wild-type plants shoot development is blocked by high hexose concentrations, but transgenic plants expressing antisense hexokinase shoot development proceeds normally). Thus transgenic plants expressing antisense hexokinase are useful for a variety of agricultural purposes including, but not limited to, the promotion of growth rate and development, seed germination, the stimulation of flowering, and improvement of crop yield, especially under adverse environmental conditions, for example, high light, high temperature, and high CO 2 In addition, the results presented above demonstrate that it is possible to modulate a plant's sensitivity to sugar by increasing levels of hexokinase protein. In particular, we found that increased levels of hexokinase protein are useful for promoting increased expression of a sugar-activated gene (for example, NR1). In this manner, various plant processes that are controlled, modulated, or activated by sugar can be regulated or manipulated by increasing the levels of hexokinase protein in a given plant cell, tissue, or organ. Such genetic engineering of gene expression is useful for enhancing storage protein accumulation and nitrogen accumulation, improving plant wounding responses and pathogen defense mechanisms, as well as for modifying pigmentation (for example, anthocyanin) of plant tissues (for example, 20 fruits and flowers) for ornamental and horticultural purposes. For example, increased expression of hexokinase is useful for manipulating or promoting the expression of a wide variety of sugar-activated genes that encode an assortment of proteins including, but not limited to, potato storage protein patatin, soybean vegetative storage protein, sporamin, proteinase inhibitor I, sucrose phosphate synthase, rice and maize sucrose synthase, chalcone synthase, and nitrate reductase.

All publications and patents mentioned in this specification are herein .incorporated by reference to the same extend as if each individual publication or patent was specifically and individually indicated to be incorporated by reference.

-41a Other Embodiments From the foregoing description, it will be apparent that variations and modifications may be made to the invention described herein to adopt it to various usages and conditions. Such embodiments are also within the scope of the following claims.

The entire disclosure in the complete specification of our Australian Patent Application No. 23429/97 is by this cross-reference incorporated into the present specification.

g a SEQUENCE LISTING GENERAL INFORMATION: APPLICANT: The General Hospital Corporation (ii) TITLE OF INVENTION: PLANT SUGAR SENSORS AND USES THEREOF (iii) NUMBER OF SEQUENCES: 13 (iv) CORRESPONDENCE

ADDRESS:

ADDRESSEE: Clark Elbing LLP

STREET:

CITY: Boston STATE: MA COUNTRY: USA

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COMPUTER READABLE FORM: MEDIUM TYPE: Floppy disk COMPUTER: IBM PC compatible OPERATING SYSTEM: PC-DOS/MS-DOS SOFTWARE: PatentIn Release Version #1.30 (vi) CURRENT APPLICATION DATA: APPLICATION NUMBER: FILING DATE:

CLASSIFICATION:

(vii) PRIOR APPLICATION DATA: APPLICATION NUMBER: US 08/622,191 FILING DATE: 25-MAR-1996

CLASSIFICATION:

(viii) ATTORNEY/AGENT

INFORMATION:

NAME: Lech, Karen F.

REGISTRATION NUMBER: 35,238 REFERENCE/DOCKET NUMBER: 00786/307W01 (ix) TELECOMMUNICATION

INFORMATION:

TELEPHONE: 617/723-6777 TELEFAX: 617/723-8962

TELEX:

-43- INFORMATION FOR SEQ I) NO: 1: SEQUENCE CHARACTERISTICS: LENGTH: 453 amino acids TYPE: amino acid STRANDEDNESS: not relevant TOPOLOGY: linear (ii) MOLECULE TYPE: protein (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 1: Met Gly Lys Val Ala Val Gly Ala Thr Val Val Cys Tbr Ala Ala Val 1 5to Cys Ala Val Ala Val Leu Val Val Mrg Arg Arg Met Gin Ser Ser Gly 25 Lys Trp Gly Arg Val Leu Ala Ile Leu Lys Ala Phe Giu Glu Asp Cys 40 Ala Thr Pro Ile Ser Lys Leu Arg Gin Val Ala Asp Ala Met Thr Val 55 Giu Met His Ala Gly Leu Ala Ser Asp Gly Gly Ser Lys Leu Lys Met 70 75 Leu Ile Ser Tyr Val Asp Asn Leu Pro Ser Gly As~p Glu Lys Giy Leu 90 it -44- Phe Tyr Ala Leu Asp Lou Gly Gly Thr Asn Phe Arg Val Met Arg Val too 105 110 Lou Leu Gly Gly Lys Gin Glu Arg Val Val Lys Gin Glu Phe Glu Glu 115 120 125 Val Ser Ile Pro Pro His Lou Met Thr Gly Gly Ser Asp Glu Lou Phe 130 135 140 Asn Phe le Ala Glu Ala Lou Ala Lys Phe Val Ala Thr Glu Cys Glu 145 150 155 160 Asp Phe His Leu Pro Glu Gly Arg Gin Arg Glu Leu Gly Phe Thr Phe 165 170 175 Ser Phe Pro Val Lys Gin Thr Ser Lou Ser Ser Gly Ser Leu le Lys 185 190 Trp, Thr Lys Gly Phe Sor le Glu Glu Ala Val Gly Gin Asp Val Vai *195 200 205 Gly Ala Leu Asn Lys Ala Lou Glu Arg Val Gly Leu Asp Met Arg le *210 215 220 Ala Ala Lou Val Asn Asp Thr Val Gly Thr Leu Ala Gly Gly Arg Tyr 225 230 235 240 Tyr Asn Pro Asp Val Val Ala Ala Vai Ile Leu Gly Thr Gly Thr Msn 245 250 255 p Ala Ala Tyr Val Giu krg Ala Tbr Ala le Pro Lys Trp His Gly Leu 260 265 270 Leu Pro Lys Ser Gly Giu Met Val Ilie Asn Met Giu Trp Gly Asn Phe 275 280 285 Arg Scr SeT His Leu Pro Lou Thr Glu Phe Asp His Tbr Leu Asp Phe 290 295 300 Glu Ser Leii Asn Pro (ily Glu Gin le Leu Glu Lys le Ile Set Gly 305 310 315 320 Met Tyr Leu Gly Glu le Lou Arg Arg Val Lou Lou Lys Met Ala Glu 325 330 335 Asp Ala Ala Phe Phe Gly Asp Thr Val Pro Ser Lys Leu Arg le Pro 340 345 350 Phe Ile Ilie Arg Tbr Pro His Met Ser Ala Met His Asn Asp Tbr Ser 355 360 365 :2>Pro Asp Leu Lys le Val Gly Ser Lys le Lys Asp le Leu Glu Val *370 375 380 Pro Thr Thr Ser Leu Lys Met Arg Lys Val Vai Ilie Ser Leu Cys Asn 385 390 395 400 Ilie Ilie Ala Thr Arg Gly Ala Arg Leu Ser Ala Ala Gly le Tyr Gly 405 410 415 -46le Leu Lys Lys Lou Gly Arg Asp Thr Thr Lys Asp Giu Glu Val Gin 420 425 430 Lys Ser Val le Ala Met Asp Gly Gly Leu Phe Glu His Tyr Thr Gin 435 440 445 Phe Ser Giu Cys Met 450 INFORMATION FOR SEQ ID) NO:2: SEQUENCE CHARACTERISTICS: LENGTH: 502 amino acids TYPE: amino acid STRANDEDNESS: not relevant TOPOLOGY: linear (ii) MOLECULE TYPE: protein (xi) SEQUENCE DESCRIPTION: SEQ ID NO:2: Met Gly Lys Val Ala Val Ala Thr Thr Val Val Cys Ser Val Ala Val 10 Cys Ala Ala Ala Ala Leu le Val Arg Arg Arg Met Lys Ser Ala Gly 25 Lys Trp Ala Mrg Val le Glu Ile Leu Lys Ala Phe Giu Giu Asp Cys *035 40 -47e. 4' Ala Tbr Pro le Ala Lys Leu Arg Gin Val Ala Asp Ala Met Thtr Val Glu Met His Ala Cily Leu Ala Set Glu Gly Gly Ser Lys Leu Lys Met Leu le Ser Tyr Val Asp Asn Leu Pro Ser Gly Asp Giu Thr Gly Phe Phe Tyr Ala Leu Asp Leu Gly Gly Thr Asn Phe Arg Val Met Arg Val Leu Leu Gly Gly Lys His Asp krg Val Val Lys Axg Glu Phe Lys Giu Glu Set le Pro Pro His Leu Met Thr Gly Lys Set His Qlu Leu Phe 4**eW*

C

6# a 9* a.

p a a.

i a a *aeg a a Sat .a a a a a a a Asp Phe le Val Asp Val Leu Ala Lys Phe Val Ala Thr Glu Gly Giu Asp Phe His Leu Pro Pro Gly krg Gin Arg Glu Leu Giy Phe Thr Phe.

165 170 175 Ser Phe Pro Val Lys Gin Leu Ser Leu Ser Ser Gly Thr Leu Ile Asn Trp Thr Lys Gly Phe Scr le Asp Asp Thr Val Asp Lys Asp Val Val -48- Gly Giu Leu Val Lys Ala Met Glu Arg Val Gly Lou Asp Met Leu Val 210 215 220 Ala Ala Lou Val Asn Asp Thr le Gly Thr Leu Ala Gly Gly Arg Tyr 225 230 235 240 Thr Asn Pro Asp Val Val Val Ala Val le Leu Gly Thr Gly Thr Asn 245 250 255 Ala Ala Tyr Val Giu Arg Ala Hfis Ala Bie Pro Lys Trp His Gly Leu 260 265 270 Leu Pro Lys Ser Gly Glu Met Val le Asn Met Glu Trp, Giy Asn Pbe 275 280 285 Mrg Ser Ser His Lou Pro Leu Thr Glu Tyr Asp His Ser Leu Asp Val .04:290 295 300 As Se S.s r l GuGnIeLuGu y l l e l @feeAs MeTr LouAsr Gly Glu Gin liergAg a Lo G u Lys i et er Gl 66830 310 315 320 Met Tya LA l Glu ie lu Mgp Il Val oP Ly Lu Lys Me AlaGo 34 3230 335 GuAAaPhe Phe Ily Asp lb alPr Pro Ly e AaMtHs Lou Ls lirer 340 345 3650 -49t.

Pro Asp Leu Lys Val Val Gly Ser Lys Leu Lys Asp le Leu Glu Val 370 375 380 Gin Thr Ser Scr Leu Lys Met Arg Lys Val Val le Ser Leu Cys Asn 385 390 395 400 le le Ala Ser Mrg Gly Ala Arg Leu Ser Ala Ala Gly lie Tyr Gly 405 410 415 le Leu Lys Lys le Gly Arg Asp Ala Thr Lys Asp Gly Glu Ala Gin 420 425 430 Lys Ser Val le Ala Met Asp Giy Gly Leu Phe Glu His Tyr Thr Gin 435 440 445 Phe Ser Glu Ser Met Lys Ser Ser Leu Lys Glu Leu Leu Gly Asp Glu 450 455 460 Vai Ser Glu Ser Val Giu Val le Leu Ser Asn Asp Gly Scr Gly Vai 45470 475 480 Gly Ala Ala Leu Leu Ala Ala Ser His 5cr Gin Tyr Leu Glu Leu Glu *485 490 495 Asp Asp Ser Giu Tbr Ser 500 INFORMATION FOR SEQ ID NO:3: SEQUENCE CHARACTERISTICS: LENGTH: 2023 base pairs TYPE: nucleic acid STRANDEDNESS: double TOPOLOGY: linear (ii) MOLECULE TYPE: DNA (xi) SEQUENCE DESCRIPTON: SEQ ED NO:3: CAGTGTGAGT AA'IMAGATC GGTATTAGAT CCATCTTAGG M='CCAAT TFCTCTCAAT TCACTCCAAA AT=GAITA T1r=CTIT CTGGCITGTC AATITAGTC ATITGTAATC 120 CTTCrM~G CGATCGGAAT CGTAAAAATIC CGATCM~CT 7rrAGATrCQ i=rrrri= 180 GA=rCAAAT CGGAAAAATG GGTAAAGTAG CTGTGGAGC GACTGrGTT TGCACGGCGG 240 CGGIITOTGC GGTGGCTGrT TTGG1TI'C GACGACGGAT GCAGAGCTCA GGGAAGTGGG 300 GACGTGTr GGCTATCCTC AAGGCCTrG AAGAGGATG TGCGACTCCG ATCT)CGAAAC 360 TGAGACAAGT GGCTGATGCT ATGACCGTI' AGATGCATGC TGGTC1TrCA TCCGACGGTG 420 *.*GTAGCAAACT CAAGATGCrr ATCAGCTACO3 TGATAATCT TCCTCCGGG GATGAAAAGG 480 GTCT'CTMTA TGCATrGGAC CTAGGGGGGA CAAACM~CG TGTCATGCGT GTGCTrCTT 540 GCGGGAAGCA AGAGCGTGfl G1TAAACAAG AA1TCGAAGA AGTCGATr CCTCCTCATr 600 TGATGACTGG TcG1TCAGAT GAGTITGTFA IITATAGC TGAAGCTC1T GCGAAG1TG 660 TCGCTACAGA ATGCGAAGAC I TATCTTC CAGAAGGTAG ACAGAGGGAA TrAGGTrTCA 720 C1TCTCGTr TCCTGTTAAG CAGACTI'CTC TGTCCTCTGG TAGTCTCATC AAATGGACAA 780 AAGGCTrrrC CATCGAAGAA GCAG7TGGAC AAGATGITGT TGGAGCAC7T AATAAGGCTC 840 TGGAAAGAGT TGGTCTTGAC ATGCGAATCG CAGCACTrGT TAATGATACC GITGGAACAC 900 TAGCCGGTGG TAGATACTAT AACCCGGATG TrGTTGCTGC TGTTAlTITA GGCACTOGGA 960 CAAACGCAGC CTATG7TGAG CGTGCAACCG CGATCCCrAA ATGGCATGGT CTGc1TCCAA 1020 AATCAGGAGA AATGGflATA AACATGGAAT GGGGAAACfl CAGGTCAT)CA CATCTrCCAT 1080 TAACCGAGIT TGATCACACG CTGGATICG AGAGTCTGjAA TCCAGGCGAA CAGA1TCTG 1140 AGAAAATCAT ITCCGGTATG TAMGGGAG AGATIMGCG AAGAGMICT CTAAAGATGG 1200 CTGAAGATGC TGCrTrCM~ GGCGATACAG TCCCATCAA GCTGAGAATA CCATrCATCA 1260 1TAGGACTCC TCACATGTCG GCTATGCACA ACGACACIT TCCAGACTTG AAGAflGT1G 1320 GGAGCAAGAT TAAGGATATA ITGGA0GGTCC CTACAACrrC TCTGAAAATG AGAAAAGTFG 1380 TGATCAGTCT CrGCAACATC ATAGCAACCC GAGGAGCrCG TCTCTCTGCT GCTGGAATCT 1440 ATGGTATTCT GAAGAAACTG GGAAGAGATA CTACTAAAGA CGAGGAGGTG CAGAAATCGG 1500 ITATAGCCAT GGATGGTGGA TrGTffGAGC ATTACACTUA G1TrAGTGAG TGTATGGAGA 1560 GCTCACTAAA AGAG ITGCTT GGAGATGXAG CTCAGGAAG CG1TGAAGTC ACTCACTCCA 1620 ATGATGGATC AGGCATTGGA GCTGCGCrrC TTGCTGCrTC TCACTCWCT TACCTTGAAG 1680 ACTCflAAAA CCTACCCAAA GAGCGCCATT 'IrGG*'AAT TTACTGAAAG C1TrTGCrA 1740 TCAGAAAACG CCrAAGCCAA GTrCTAAGGC GTCATAAAAG AAAGCA1TCC ATrT=~AC 1800 TCTrCCCCAA GAcFI1clTr GTAGCAAATA AG11TCCTTG GCAGAAATAT TTGTM~CAT 1860 GTCT1CAAA AATAAAAGAC TCAGTTC1TC AGA1TCTGGG ATTlTATTAT AdkCCAGATAT 1920 GTTGTAAAAA CTACAAATTC AAAGCTrCACT TCACTGGAGT TCTGAGTATA TAAAGAT17C 1 980 -52- ATrTrrCCTA AAAAAAAAAA AAAAAACTAA ATTACrCACA MT 2023 INFORMATION FOR SEQ ID NO: SEQUENCE CHARACTERISTICS: LENGTH: 1883 base pairs TYPE: nucleic acid STRANDEDNESS: double TOPOLOGY: linear (ii) MOLECULE TYPE: DNA (xi) SEQUENCE DESCRIPTION: SEQ ID NO: CAGTGTGAGT AATITAGATC ATCrTAGCG TC'rAAAGT TTCCAACITI' T1T1TITAT TAAMTGGGC CAACTTI GITTATTAA TTMGGCCAA CCT1T=G0 1TGAGAATT 120 GGGCOAGGGA GAAAGATGGG TAAAGTGGCA G1TGCAACGA CGGTAGTGTG TrCGGTGGCG 180 GTATGTGCGG CGGCGGCGI7 GATAGTACGG AGGAGAATGA AAAGCGCAGG GAAATGGGCA 240 AGAGTGATAG AGATA11TGAA AGCCTTTGAA GAAGA11'OTG CAACGCCAAT TGCCAAAfld5 300 AGACAAGTGG CTGATGCTAT GACTOiTTOAG ATGCATGCTG GTCITGCTrC TGAAGGTGGC 360 AGCAAGCITA AGATGCTTAT TAGCTrACGTT GATAATCTI'C CTTCTGGGGA TGjAGACTGGT 420 7r1TCTATG CGTTGGATCT AGGCGGAACA AAC1TCCGTG TrATGCGTGT GCrtCITGGT 480 GGGAAGCACG ACTGTrGT TAAACGAGAA TrCAAAGAAG AATCTA1TCC TCCTCA1TI'G 540 *ATGACCGGrGA AGTCACATGA ArrATTCGAT 1TATCG1TG ATGTTCTTGC CAAGTrrGTC 600 GCTACAGAAG GCGAGGACT1' TCATCTCCCA CCTGGTAGAC AACGGGAACT AGGTTTCACT 660 -53- TTCTCATTC CG1TAAGCA GCTATC1TFA TCCTCTGIGCA CTCTCATCAA CTGGACAAAG 720 GGCITITCCA 1TGACGATAC AGrrGATAAA GATGTrGTFG GAGAAC'ITGT TAAAGCTATG 780 GAAAGAGT1'G GGCTGGACAT GCTTGTCGCA GC1TGTTA ATGATACCAT TGGAACACTT 840 GCGGGTGGTA GATACACTAA CCCGGATGTC GTTGTCGCAG 11'ATMGGG CACCGGCACA 900 AATGCAGCCT ATGTCGAACG TGCACATGCA ATTCCCAAAT GGCATGG'TTT GCTACCCAAA 960 TCAGQAGAAA TGGTGATCAA CATGGAATGG GGAAAc-rcA GGTCATCACA TCnTCATI'G 1020 ACAGAGTACG ACCACTCTCT AGATGTcGAT AGTrGAATC CTGGTGAACA GATTCTlGAG 1080 AAAATCA1TTT CCGGAATGTA TCTGGGAGAA AT=fGCGTA GACJ1TCTTCT GAAGATGGCT 1140 GAAGAAGCTG CCrTTC=G CGATATCGTC CCACCTAAGC TGAAAATACC A77CA4TCATA 1200 AGGACCCOCA ACATGTCTGC TATGCACAGT GATACTTCCC CGGA=T'AA GGTTGTAGGA 1260 AGCAAGTI'AA AAGACATAfl GGAGGTCCAG ACTAGT17CTC TGAAGATGAG GAAAGTGTG 1320 **ATCAGCCTAT GTAACATCAT TGCAAGCCGA GGAGCTCGTT TATCTGCTGC GGGGATCTAT 1380 *GGAATCCTCA AGAAAATAGG AAGAGACGCA ACAAAAGATQ GAGAAGCTCA GAAATCTGTG 1440 ATAGCGATGG AGGTGGGCT ArT1CGAGCAT TACACTCAGT TCAGTGAGTC GATGAAGAGT 1500 TCATTGAAAG AGTrGCITGG AGATGAAGTT TCAGAGACO T7GAAGTGAT ACTGTCGAAT 1560 GATGGTTCAG GTGTrGGAGC TGCATI'ACTT GC1'GCTTCTC ACITCTCAGTA TCTCGAACTT 1620 GAA6ATGACT CTGAAACAAG 11TAATrAAA Gc1TTTTGT GITT'AACC'I7 CflrflGfG 1680 CGTAGGTTAA CAATAAAAGT AGAGGTAA AT GCCTIGGGA AAI IIAMT TTGACAATn' 1740 TCAGGAACAA TAAAACCTGG A1TCTfrCATC AAAGCTCTGG GAAATTCAAA CGACCAGCCA 1800 ATG1TGTAGA ACTATACATA TATATTCGAG TTCT1TCTAT GAAAAAAAAA AAAAAAAAAA 1860 6-54- 9. I, AACCrTAAAT TAMfACACT GGC 1883 INFORMATION FOR SEQ ID, NO: SEQUENCE CHARACTERISTICS: LENGTH: 465 amino acids TYPE: amino acid STRANDEDNESS: not relevant TOPOLOGY: linear (ii) MOLECULE TYPE: protein (xi) SEQUENCE DESCRIPTION: SEQ ID) Met Leu Asp Asp Arg Ala krg Met Glu Ala Ala Lys Lys Glu Lys Val 1 5 10 Gin Gin le Leu Ala Glu Phe Gin Leu Gin Glu Glu Asp Leu Lys Lys *20 25 Val Met krg krg Met Gin Lys Glu Met Asp krg Gly Leu krg Leu Glu 5..35 40 Thr His Glu Glu Ala Ser Val Lys Met Leu Pro Tin Tyr Val Arg Ser 55 Thr Pro Glu Gly Ser Glu Val Gly Asp Phe Leu Ser Leu Asp Leu Gly 70 75 Gly Thir Asn Phe Arg Val Met Leu Val Lys Val Gly Glu Gly Glu Giu 90 Gly Gin Trp Ser Val Lys Thr Lys His Gin Met Tyr Ser le Pro Glu 100 105 110 Asp Ala Met Tbr Gly Thr Ala Giu Met Leu Phe Asp Tyr Ile Ser Glu 115 120 125 Cys le Ser Asp Phe Leu Asp Lys His Gin Met Lys His Lys Lys Leu 130 135 140 Pro Leu Gly Phe Thr Phe Ser Phe Pro Vai Arg His Glu Asp le Asp 145 150 155 160 Lys Gly Ile Leu Leu Asn Gin Thr Lys Gly Phe Lys Ala Ser Gly Ala 165 170 175 Giu Gly Asn Asn Val Val Gly Leu Leu Arg Asp Ala le Lys Arg Arg 180 185 190 Gly Asp Phe Glu Met Asp Val Val Ala Met Val Asn Asp Thr Val Ala *195 200 205 .o 0000.Thr Met Ile Ser Cys Tyr Tyr Glu Asp His Gin Cys Glu Val Gly Met 0:00 210 215 220 225 0 0.

le Val Gly Thr Gly Cys Asn Ala Cys Tyr Met Glu Gin Met Gin Asn 230 235 240 -56- Vat Giu Leu Vat Glu Gly Asp Giu Gly Arg Met Cys Val Asn Thr Giu 245 250 255 Gin Gly Ala Phe Gly Asp Sex Gly Giu Leu Asp Glu Phe Leu Leu Glu 260 265 270 Tyr Asp Arg Met Val Asp Giu Ser Ser Ala Asn Pro Gly Gin Gin Leu 275 280 285 Tyr Glu Lys Leu Ile Gly Gly Lys Thr Met Gly Giu Leu Val Arg Leu 290 295 300 305 Val Leu Leu Arg Leu Val Asp Giu Asn Leu Leu Phe His Gly Glu Ala 310 315 320 Ser Glu Gin Leu Mrg Thr Arg Gly Ala Phe Giu Thr Arg Phe Val Ser **325 330 335 Gin Val Glu Ser Asp Thr Gly Asp Mrg Lys Gin le Tyr Asn le Leu :340 345 350 Ser Tbr Leu Gly Leu Arg Pro Ser Thr Thr Asp Cys Asp le Val Arg *355 360 365 Arg Ala Cys Giu Ser Val Ser Thr Mrg Ala Ala His Met Cyg Ser Ala *370 375 380 385 Gly Leu Ala Gly Val Ie Asn Arg Met Arg Glu Ser Mrg Ser Glu Asp 390 395 400 -57- Val Met Arg le Thr Val Gly Val Asp Gly Ser Val Tyr Lys Leu His 405 410 415 Pro Ser Phe Lys Glu Arg Phe His Ala Ser Val Arg Arg Leu Thr Pro 420 425 430 Ser Cys Glu Ile Thr Phe le Giu 5cr Giu Glu Gly Ser Gly Mg Gly 435 440 445 Ala Ala Leu Val Ser Ala Val Ala Cys Lys Lys Ala Cys Met Leu Gly 450 455 460 465 Gin INFORMATION FOR SEQ ID NO:6: SEQUENCE CHARACTERISTICS: LENGTH: 465 amino acids (13) TYPE: amino acid STRANDEDNESS: not relevant TOPOLOGY: linear (ii) MOLECULE TYPE: protein (xi) SEQUENCE DESCRIPTION: SEQ ID NO:6: Met Ala Met Asp Thr Thr Arg Cys Gly Ala Gin Leu Leu Thr Leu Val *51 5 10 Glu Gin le Leu Ala Glu Phe Gln Leu Gin Glu Glu Asp Leu Lys Lys 25 -58- Val Met Ser Arg Met Gin Lys Glu Met Asp Arg Gly Leu Arg Leu Glu 40 Thr His Glu Glu Ala Ser Vat Lys Met Leu Pro Thr Tyr Val Arg Ser 55 Thr Pro Gin Gly Ser Glu Vat Gly Asp Phe Leu Ser Leu Asp Leu Gly 70 75 Gly Thr Asn Phe Arg Val Met Leu Vat Lys Val Gly Glu Gly Glu Ala 90 Gly Gin Trp Ser Vat Lys Thr Lys His Gln Met Tyr Ser le Pro Glu 100 105 110 Asp Ala Met Thr Gly Thr Ala Glu Met Leu Ph e Asp Tyr le Ser Glu 115 120 125 Cys le Ser Asp Phe Leu Asp Lys His Gin Met Lys His Lys Lys Leu :130 135 140 0 Pro Leu Gly Phe Thr Phe Ser Phe Pro Val Arg His Glu Asp Leu Asp o o145 150 155 160 o 00*9 oLys Gly le Leu Leu Asn Trp Thr Lys Gly Phe Lys Ala Ser Gly Ala o:o 165 170 175 00: Glu Gly Asn Asn le Val Gly Leu Leu Arg Asp Ala Ile Lys Mrg Arg 180 185 190 -59- 4.

Gly Asp Phe Glu Met Asp Val Val Ala Met Val Asn Asp Thr Vat Ala 195 200 205 Thr Met lie Ser Cys Tyr Tyr Glu Asp krg Gin Cys Glu Val Gly Met 210 215 220 lie Val Gly Thr Gly Cys Asn Ala Cys Tyr Met Glu Glu Met Gin Asn 225 230 235 240 Vat Glu Leu Val Glu Gly Asp Glu Gly Arg Met Cys Val Asn Thr Giu 245 250 255 Trp Gly Ala Phe Gly Asp Ser Gly Glu Leu Asp Glu Phe Leu Leu Glu 260 265 270 Tyr Asp Arg Met Vat Asp Glu Ser Ser Ala Asn Pro Gly Gin Gin Leu 275 280 285 Tyr Glu Lys Ilie Ile Gly Gly Lys Tyr Met Gly Glu Leu Val Arg Leu 290 295 300 Val Leu Leu Lys Leu Val Asp Glu Asn Leu Leu Phe His Gly Giu Ala 305 310 315 320 Set Glu Gin Leu Arg Thr Arg Gly Ala Phe Glu Thr Arg Phe Val Ser 325 330 335 Gin Val Gin Set Asp Ser Gly Asp Arg Lys Gin Ile His Asn le Leu 340 345 350 Ser Thr Leu Gly Leu Arg Pro 5cr Val Tbr Asp Cys Asp le Val Mrg 355 360 365 Arg Ala Cys Glu Ser Val Ser Thr Mg Ala Ala His Met Cys Ser Ala 370 375 380 Gly Leu Ala Gly Val Ile Asn Arg Met Arg Glu Ser Arg Ser Giu Asp 385 390 395 400 Val Met Mrg Ile Thr Val Gly Val Asp Gly Ser Val Tyr Lys Leu His 405 410 415 Pro Ser Phe Lys Glu Arg Phe His Ala Ser Val Arg Arg Leu Thr Pro 420 425 430 Asn Cys Glu le Thr Phe le Glu Ser Glu Glu Gly Scr Gly Arg Gly *435 440 445 Ala Ala Leu Val Ser Ala Val Ala Cys Lys Lys Ala Cys Met Leu Ala 450 455 460 Gin 465 INFORMATION FOR SEQ ID NO:7: SEQUENCE CHARACTERISTICS: LENGTH: 486 amino acids TYPE: amino acid STRANDEDNESS: not relevant 61- TOPOLOGY: linear (ii) MOLECULE TYPE: protein (xi) SEQUENCE DESCRIPTION: SEQ ID NO:7: Met Val His Leu Gly Pro Lys Lys Pro Gin Ala Arg Lys Gly Ser Met 0 *9 0 Ala Asp Val Pro Lys Glu Leu Met Asp Glu le His Gin Leu Glu Asp 25 Met Phe Thr Val Asp Ser Giu Thr Leu Arg Lys Val Val Lys His Phe 40 le Asp Glu Leu Asn Lys Gly Leu Thr Lys Lys Gly Val Asn le Pro 55 Met le Pro Gly Trp Val Met Gin Phe Pro Thr Gly Lys Glu Ser Gly 65 70 75 Asn Tyr Leu Ala Ile Asp Leu Gly Giy Thr Asn Leu Arg Val Val Leu 90 Val Lys Leu Ser Gly Asn Mrg Thr Phe Asp Thr Thr Gin Ser Lys Tyr Lys Leu Pro His Asp Met Arg Thr Thr Lys His Gin Glu Giu Leu Trp 115 120 125 -62- Ser Phe le Ala Asp Ser Leu Lys Asp Phe Met Val GLu Gin Glu Leu Leu Asn Thr Lys Asp Thir Leu Pro Leu Gly Phe Thr Phe Ser Tyr Pro Ala Ser Gin Asn Lys bLe Asn Glu Gly le Leu Gin Arg Trp Thr Lys -63- Gly Phe Asp lie Pro Asn Val Glu Gly His Asp Val Val Pro Leu Leu 180 185 190 Gin Lys Glu le Ser Lys Arg Giu Leu Pro le Glu le Val Ala Leu 195 200 205 le Asn Asp Tbr Val Gly Thr Leu Ile Ala Ser Tyr Tyr Thr Asp Pro 210 215 220 Giu Thr Lys Met Gly Val le Phe Gly Tiir Gly Val Asn Gly Ala Phe 225 230 235 240 Tyr Asp Val Cys Ser Asp le Giu Lys Leu Glu Gly Lys Leu Ala Asp 245 250 255 Asp le Pro Ser Asn Ser Pro Met Ala lie sn. Cys Gli Tyr Gly Ser S260 265 270 Asp Asn Giu His Leu Vai Leu Pro krg Thr Lys Tyr Asp Val Ala 275 280 285 Val Asp Giu Gin Ser Pro Arg Pro Gly Gin Gin Ala Phe Glu Lys Met 290 295 300 Thr Ser Gly Tyr Tyr Leu Gly Glu Leu Leu Arg Leu Val Leu Leu Glu 305 310 315 320 Leu Asn Glu Lys Gly Leu Met Leu Lys Asp Gin Asp Leu Ser Lys Leu 325 330 335 -64- Lys Gin Pro Tyr lie Met Asp Tbr Ser Tyr Pro Ala Arg Ile Glu Asp 340 345 350 Asp Pro Phe Glu Asn Leu Glu Asp Thr Asp Asp Met Phe Gin Lys Asp 355 360 365 Phe Gly Val Lys Tlir Thr Leu Pro Glu Arg Lys Leu Ile Arg Arg Leu 370 375 380 Cys Giu Leu le Gly Thr Arg Ala Ala Arg Leu Ala Val Cys Gly lie 385 390 395 400 Ala Ala lie Cys Gin Lys Arg Gly Tyr Lys Thr Gly His le Ala Ala 410 415 Asp Giy Ser Val Tyr Asn Lys Tyr Pro Gly Phe Lys Giu Ala Ala Ala 420 425 430 Lys Gly Leu Mrg Asp Ile Tyr Gly Trp Thr Gly Glu Asn Ala Ser Lys 435 440 445 Asp Pro le Thr le Val Pro Ala Glu Asp Gly Ser Gly Ala Gly Ala 450 455 460 Ala Val le Ala Ala Leu Ser Giu Lys Mrg lie Ala Glu Giy Lys Val 465 470 475 480 Ser Gly lie le Gly Ala 485 INFORMATION FOR SEQ ID NO:8: SEQUENCE CHARACTERISTICS: LENGTH: 486 amino acids TYPE: amino acid STRANDEDNESS: not relevant TOPOLOGY: linear (ii) MOLECULE TYPE: protein (xi) SEQUENCE DESCRIPTION: SEQ ID NO:8: Met Val His Leu Gly Pro Lys Lys Pro Gin Ala Arg Lys Gly Ser Met 1 5 10 Ala Asp Val Pro Lys Glu Leu Met Gin Gin lie Giu Asn Phe Giu Lys 25 Sle Phe Thr Val Pro Thr Giu Thr Leu Gin Ala Val Thr Lys His Phe 40 *~.lie Ser Glu Leu Glu Lys Gly Leu Ser Lys Lys Gly Gly Asn le Pro so 55 Met le Pro Gly Trp Val Met Asp Phe Pro Thr Gly Lys Glu Set Gly 70 75 Asn Tyr Leu Ala le Asp Leu (fly Gly Thr Asn Leu Arg Val Val Leu 90 Val Lys Leu Gly Gly Asp Arg Thr Phe Asp Thr Thr Gin Ser Lys Tyr 100 105 110 -66- Mrg Leu Pro Asp Ala Met Arg Thr Thr Gin Asn Pro Asp Giu Leu Trp, 115 120 125 Giu Phe le Ala Asp Ser Leu Lys Ala Phe le Asp Glu Gin Phe Pro 130 135 140 Gin Gly le Ser Glu Pro le Pro Leu Gly Phe Thr Phe Ser Tyr Pro 145 150 155 160 Ala Ser Gin Asn Lys Ie Asn Glu Gly le Leu Gin Arg Trp Tbr Lys 165 170 175 Gly Phe Asp le Pro Asn Val Giu Gly His Asp Val Vai Pro Leu Leu 180 185 190 Gin Lys Glu le Ser Lys Arg Giu Leu Pro le Glu Cys Cys Ala Leu 195 200 205 *Ile Asn Asp Thr Thr Gyly Thr Leu Val Ala Ser Tyr Tyr Thr Asp Pro 210 215 220 Glu Thr Lys Met Gly Val le Phe Gly Thr Gly Val Asn Gly Ala Tyr 225 230 235 240 Tyr Asp Val Cys Ser Asp le Glu Lys Leu Trp Gly Lys Leu Ser Asp 9.**245 250 255 -67- Asp le Pro Pro Ser Ala Pro Met Ala Ile Asn Cys Glu Tyr Gly Ser 260 265 270 Phe Asp Asn Giu His Val Val Leu Pro Arg Thr Lys Tyr Asp Ile Thr le Asp Cilu Giu Ser Pro Arg Pro Gly Trp Trp Thr Phe Glu Lys Met 290 295 300 Scr Ser Gly Tyr Tyr Leu Gly Glu le Leu Mrg Leu Ala Leu Met Asp 310 Met Tyr Lys Gin Gly Phe le Phe Lys Asn Gin Asp Leu Ser Lys Phe 325 Asp Lys Pro Phe Val Met Asp Thr Ser Tyr Pro Ala Arg le Glu Glu 340 345 350 Asp Pro Phe Glu Asn Leu Giu Asp Thr Asp Asp Leu Phe Gin Asn Glu 355 360 365 Phe Gly Ile Asn Thr Thr Val Gin Glu Arg Lys Leu le Kg Ag Leu 370 375 Ser Glu Leu le Gly Ala Mrg Ala Ala Arg Leu Ser Val Cys Gly le Ala Ala le Cys Gin Lys Mrg Gly Tyr Lys Thr Giy His le Ala Ala 405 410 415 -68- Asp Gly Ser Val Tyr Asn Arg Tyr Pro Gly Phe Lys Glu Lys Ala Ala 420 425 430 Asn Ala Leu Lys Asp le Tyr Gly Trp Tbr Gin Thr Set Leu Asp Asp 435 440 445 Tyr Pro Ile Lys le Val Pro Ala Glu Asp 3 iy Ser Gly Ala Gly Ala 450 455 460 Ala Val Ilie Ala Ala Leu Ala Gin Lys Arg le Ala Glu Gly Lys Set 465 470 475 480 Val Gly le le Gly Ala 485 INFORMATION FOR SEQ ID NO:9: SEQUENCE CHARACTERISTICS: LENGTH: 485 amino acids TYPE: amino acid STRANDEDNESS: not relevant TOPOLOGY: linear MOLECULE TYPE: protein (xi) SEQUENCE DESCRIPTION: SEQ ID NQ:9: Met Val krg Leu Gly Pro Lys Lys Pro Pro Ala Arg Lys Gly Set Met 1 5 10 -69- Ala Asp Val Pro Ala Asn Leu Met Glu Gin Ile His Gly Leu Glu Thr 25 Leu Phe Thr Val Ser Ser Glu Lys Met Arg Ser Ile Val Lys His Phe 40 le Ser Glu Leu Asp Lys Gly Lou Ser Lys Lys Gly Gly Asn le Pro eq

C

C.

C

e.

C.

C

*Met le Pro Gly Tip Val Val Glu Tyr Pro Thr Gly Lys Glu Thr Gly 70 75 Asp Phe Lou Ala Lou Asp Leu Gly Gly Thr Asn Lou Arg Val Val Leu 90 Val Lys Leu (lly Gly Asn His Asp Phe Asp Tyr Tyr Gin Asn Lys Tyr 100 105 110 Arg Lou Pro Asp His Leu Arg Thr Gly Thr Ser Glu Gin Leu Trp Ser 115 120 125 Phe le Ala Lys Cys Leu Lys Giu Phe Vai Asp Glu Trp Tyr Pro Asp 130 135 140 Gly Val Ser Glu Pro Leu Pro Leu Gly Phe Thr Phe Ser Tyr Pro Ala

C*

C

C.

CC CCC

C

Ser. Gin Lys Lys Ile Asn Ser Gly Val Leu Gin Arg Trp Thr Lys Gly 165 170 175 Phe Asp le Glu Gly Val Giu Gly His Asp Val Val Pro Met Leu Gin 180 185 190 Glu Gln le Giu Lys Leu Asn le Pro le Asn Val Val Arg Leu le 195 200 205 Asn Asp Thr Thr Gly Thr Leu Val Ala Set Leu Tyr Thr Asp Pro Gin 210 215 220 Thr Lys Met Gly le Ie le Gly '[hr Gly Val Asn Gly Ala Tyr Tyr 225 230 235 240 Asp Val Val Ser Gly le Giu Lys Leu Glu Gly Leu Leu Pro Glu Asp 245 250 255 Sle Gly Pro Asp Ser Pro Met Ala le Asn Cys Giu Tyr Gly Ser Phe set,' 260 265 270 Asp Asn Giu Gly Leu Val Leu Pro Mrg Tbr Lys Tyr Asp Val le le 275 280 285 Asp Gin Glu Set Pro Mrg Pro Gly Gin Gin Ala Phe Gin Lys Met Thr 6 9 290 295 300 Ser Giy Tyr Tyr Lou Gly Giu le Met Arg Leu Val Lou Lou Asp Lou 305 310 315 320 -71- Tyr Asp Ser Gly Phe Ile Phe Lys Asp Gin Asp le Ser Lys Leu Lys 325 330 335 Giu Ala Tyr Val Met Asp Thr Ser Tyr Pro Ser Lys le Glu Asp Asp 340 345 350 Pro Phe Glu Asn Leu Glu Asp Thr Asp Asp Leu Phe Lys Thr Asn Leu 355 360 365 Asn le Giu Thr Thr Val Val Glu Arg Lys Leu le Arg Lys Leu Ala 370 375 380 Giu Leu Vai Gly Tbr Mrg Ala Ala Arg Leu Thr Val Cys Gly Val Ser 385 390 395 400 Ala Ile Cys Asp Lys Mrg Gly Tyr Lys Thr Ala His le Ala Ala Asp 405 410 415 Gly Ser Val Phe Asn Mrg Tyr Pro Giy Tyr Lys Giu Lys Ala Ala Gin 420 425 430 Ala Leu Lys Asp le Tyr Msn Trp Asp Val Glu Lys Met Glu Asp His 435 440 445 Pro Ile Gin Leu Val Ala Ala Giu Asp Gly Ser Gly Val Gly Ala Ala 450 455 460 le le Ala Cys Leu Thr Trp Lys Mrg Leu Ala Ala Giy Lys Ser Val 465 470 475 480 -72- Gly Ile Lys Gly Glu 485 INFORMATION FOR SEQ ID SEQUENCE CHARACTERISTICS: LENGTH: 18 base pairs TYPE: nucleic acid STRANDEDNESS: single TOPOLOGY: linear (ii) MOLECULE TYPE: DNA (xi) SEQUENCE DESCRIPTION: SEQ ID ATGGGTAAAG TAGCTGTT 18 INFORMATION FOR SEQ ID NO: 11: SEQUENCE CHARACTERISTICS: LENGTH: 22 base pairs TYPE: nucleic acid STRANDEDNESS: single TOPOLOGY: linear (ii) MOLECULE TYPE: DNA (xi) SEQUENCE DESCRIPTION: SEQ ID NO:11: .0 ATGGGTAAAG TGGCAGTTGC AA 22 0.:ooo -73- INFORMATION FOR SEQ ID NO:12: SEQUENCE CHARACTERISTICS: LENGTH: 21 base pairs TYPE: nucleic acid STRANDEDNESS: single TOPOLOGY: linear (ii) MOLECULE TYPE: DNA (xi) SEQUENCE DESCRIPTION: SEQ ID NO:12: TTAAGAGTCT TCAAGGTAGA G 21 INFORMATION FOR SEQ ID NO:13: SEQUENCE CHARACTERISTICS: LENGTH: 24 base pairs TYPE: nucleic acid STRANDEDNESS: single TOPOLOGY: linear (ii) MOLECULE TYPE: DNA (xi) SEQUENCE DESCRIPTION: SEQ ID NO:13: TTAACTTGTT TCAGAGTCAT CTTC 24 -74-

Claims (32)

1. A plant comprising a transgene that encodes a hexokinase polypeptide that dominantly interferes with sugar signalling in said plant.

2. A plant according to claim 1, wherein said hexokinase polypeptide comprises a yeast hexokinase polypeptide.

3. A plant according to claim 1 or claim 2, wherein said hexokinase polypeptide has catalytic activity.

4. A plant according to any one of claims 1 to 3, wherein said hexokinase polypeptide lacks a regulatory function for sugar signalling in said plant.

A plant according to any one of claims 1 to 4, wherein said plant is less sensitive to sugar.

6. A plant according to any one of claims 1 to wherein said hexokinase polypeptide competes with an endogenous hexokinase of said plant for sugar binding.

7. A plant according to any one of claims 1 to 6, wherein said plant is a monocot or dicot.

8. A plant according to any one of claims 1 to 6, wherein said plant is maize, rice, or wheat.

9. A plant according to any one of claims 1 to 6, wherein said plant is oilseed rape or cotton. A plant according to any one of claims 1 to 9, wherein said transgene is expressed under the control of a constitutive or regulated promoter.

F:\jnelson\keep\retype\PLANT SUGAR SENSORS AND USES THEREOF P39902 CLAIM PAGES.doc 76

11. A seed or cell of a plant according to any one of claims 1 to

12. A seed or cell according to claim 11, wherein said seed or cell is a seed or cell of maize, rice, or wheat.

13. A seed or cell according to claim 11, wherein said seed or cell is a seed or cell of oilseed rape or cotton.

14. A plant expression vector comprising a transgene comprising a plant promoter operably linked to a DNA sequence that encodes a hexokinase polypeptide that dominantly interferes with sugar signalling in a plant cell.

15. A plant expression vector according to claim 14, 20 wherein said hexokinase polypeptide comprises a yeast hexokinase.

16. A plant expression vector according to claim 14 or claim 15, wherein said hexokinase polypeptide has catalytic activity.

17. A plant expression vector according to any one of claims 14 to 16, wherein said hexokinase polypeptide lacks a regulatory function for sugar signalling in said plant.

18. A plant expression vector according to any one of claims 14 to 17, wherein said hexokinase polypeptide competes with an endogenous hexokinase of said plant cell for sugar binding.

19. A method for modulating sugar sensitivity in a plant cell, said method comprising the steps of: F:\jnelson\keep\retype\PLANT SUGAR SENSORS AND USES THEREOF P39902 CLAIM PAGES.doc 77 introducing into a plant cell a transgene that encodes a hexokinase polypeptide that dominantly interferes with sugar signalling in said plant cell; and expressing said transgene in said plant cell, wherein expression of said transgene modulates sugar sensitivity in said plant cell.

A method according to claim 19, wherein said hexokinase comprises a yeast hexokinase polypeptide.

21. A method according to claim 19 or claim wherein said hexokinase polypeptide has catalytic activity.

22. A method according to any one of claims 19 to 21, wherein said hexokinase polypeptide lacks a regulatory function for sugar signalling in said plant.

23. A method according to any one of claims 19 to 22, further comprising regenerating a plant from said plant 20 cell.

24. A method according to claim 23, wherein said plant is less sensitive to sugar.

25. A method according to claim 23 or claim 24, wherein said hexokinase polypeptide competes with an endogenous hexokinase of said plant for sugar.

26. A method according to any one of claims 23 to 30 wherein said plant is a monocot or dicot.

*27. A method according to any one of claims 23 to wherein said plant is maize, rice, or wheat.

28. A method according to any one of claims 23 to ,gg=g wherein said plant is oilseed rape or cotton. F:\jnelson\keep\retype\PLANT SUGAR SENSORS AND USES THEREOF P39902 CLAIM PAGES.doc 78

29. A plant according to any one of claims 19 to 28, wherein said transgene is expressed under the control of a constitutive or regulated promoter.

30. A plant according to claim 1, substantially as herein described with reference to any one of the Examples.

31. An expression vector according to claim 14, substantially as herein described with reference to any one of the Examples.

32. A method according to claim 19, substantially as herein described with reference to any one of the Examples. Dated this 28th day of January 2003 THE GENERAL HOSPTTAL CORPORATTON By their Patent Attorneys GRIFFITH HACK Fellows Institute of Patent and 20 Trade Mark Attorneys of Australia o *9.o *9* H:\jnelson\keep\retype\PLANT SUGAR SENSORS AND USES THEREOF P39902 CLAIM PAGES.doc