Abstract
Expression of a beta-amylase gene of Arabidopsis thaliana (AT beta-Amy) is regulated by sugars. We identified a mutant, hba1, in which the level of expression of AT beta-Amy in leaves of plants that had been grown in a medium with 2% sucrose was significantly higher than that in wild-type plants. Higher that wild-type levels of beta-amylase in hba1 plants depended on the presence of 1 to 2% sucrose or 1% glucose in the medium, whereas leaves of mutant plants grown with higher levels of sugars had beta-amylase activities similar to those in leaves of wild-type plants. The hba1 phenotype was recessive and did not affect levels of sugars and starch in leaves. It is proposed that expression of AT beta-Amy is regulated by a combination of both positive and negative factors, dependent on the level of sugars, and that HBA1 might function to maintain low-level expression of AT beta-Amy until the level of sugars reaches some high level. Results of crosses of hba1 plants with transgenic plants that harbored an AT beta-Amy:GUS transgene with 1587 bp of the 5'-upstream region suggested that HBA1 affects expressions of AT beta-Amy in trans. The hba1 plants also had growth defects and elevated levels of anthocyanin in their petioles. However, sugar-related changes in levels of several mRNAs other than beta-amylase mRNA were unaffected in hba1 plants, suggesting that only a subset of sugar-regulated genes is under the control HBA1.
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- Bradshaw H. D., Jr, Hollick J. B., Parsons T. J., Clarke H. R., Gordon M. P. Systemically wound-responsive genes in poplar trees encode proteins similar to sweet potato sporamins and legume Kunitz trypsin inhibitors. Plant Mol Biol. 1990 Jan;14(1):51–59. doi: 10.1007/BF00015654. [DOI] [PubMed] [Google Scholar]
- Caspar T., Lin T. P., Monroe J., Bernhard W., Spilatro S., Preiss J., Somerville C. Altered regulation of beta-amylase activity in mutants of Arabidopsis with lesions in starch metabolism. Proc Natl Acad Sci U S A. 1989 Aug;86(15):5830–5833. doi: 10.1073/pnas.86.15.5830. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Epstein P. N., Boschero A. C., Atwater I., Cai X., Overbeek P. A. Expression of yeast hexokinase in pancreatic beta cells of transgenic mice reduces blood glucose, enhances insulin secretion, and decreases diabetes. Proc Natl Acad Sci U S A. 1992 Dec 15;89(24):12038–12042. doi: 10.1073/pnas.89.24.12038. [DOI] [PMC free article] [PubMed] [Google Scholar]
- German M. S. Glucose sensing in pancreatic islet beta cells: the key role of glucokinase and the glycolytic intermediates. Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):1781–1785. doi: 10.1073/pnas.90.5.1781. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Graham I. A., Denby K. J., Leaver C. J. Carbon Catabolite Repression Regulates Glyoxylate Cycle Gene Expression in Cucumber. Plant Cell. 1994 May;6(5):761–772. doi: 10.1105/tpc.6.5.761. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hattori T., Yoshida N., Nakamura K. Structural relationship among the members of a multigene family coding for the sweet potato tuberous root storage protein. Plant Mol Biol. 1989 Nov;13(5):563–572. doi: 10.1007/BF00027316. [DOI] [PubMed] [Google Scholar]
- Jang J. C., Sheen J. Sugar sensing in higher plants. Plant Cell. 1994 Nov;6(11):1665–1679. doi: 10.1105/tpc.6.11.1665. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Johnson R., Ryan C. A. Wound-inducible potato inhibitor II genes: enhancement of expression by sucrose. Plant Mol Biol. 1990 Apr;14(4):527–536. doi: 10.1007/BF00027498. [DOI] [PubMed] [Google Scholar]
- Koch K. E., Nolte K. D., Duke E. R., McCarty D. R., Avigne W. T. Sugar Levels Modulate Differential Expression of Maize Sucrose Synthase Genes. Plant Cell. 1992 Jan;4(1):59–69. doi: 10.1105/tpc.4.1.59. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lizotte P. A., Henson C. A., Duke S. H. Purification and Characterization of Pea Epicotyl beta-Amylase. Plant Physiol. 1990 Mar;92(3):615–621. doi: 10.1104/pp.92.3.615. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mita S., Suzuki-Fujii K., Nakamura K. Sugar-inducible expression of a gene for beta-amylase in Arabidopsis thaliana. Plant Physiol. 1995 Mar;107(3):895–904. doi: 10.1104/pp.107.3.895. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Müller-Röber B. T., Kossmann J., Hannah L. C., Willmitzer L., Sonnewald U. One of two different ADP-glucose pyrophosphorylase genes from potato responds strongly to elevated levels of sucrose. Mol Gen Genet. 1990 Oct;224(1):136–146. doi: 10.1007/BF00259460. [DOI] [PubMed] [Google Scholar]
- Nakamura K., Ohto M. A., Yoshida N., Nakamura K. Sucrose-Induced Accumulation of beta-Amylase Occurs Concomitant with the Accumulation of Starch and Sporamin in Leaf-Petiole Cuttings of Sweet Potato. Plant Physiol. 1991 Jul;96(3):902–909. doi: 10.1104/pp.96.3.902. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ohto M. A., Nakamura-Kito K., Nakamura K. Induction of Expression of Genes Coding for Sporamin and beta-Amylase by Polygalacturonic Acid in Leaf-Petiole Cuttings of Sweet Potato. Plant Physiol. 1992 Jun;99(2):422–427. doi: 10.1104/pp.99.2.422. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ohto Ma., Nakamura K. Sugar-Induced Increase of Calcium-Dependent Protein Kinases Associated with the Plasma Membrane in Leaf Tissues of Tobacco. Plant Physiol. 1995 Nov;109(3):973–981. doi: 10.1104/pp.109.3.973. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ozcan S., Johnston M. Three different regulatory mechanisms enable yeast hexose transporter (HXT) genes to be induced by different levels of glucose. Mol Cell Biol. 1995 Mar;15(3):1564–1572. doi: 10.1128/mcb.15.3.1564. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rocha-Sosa M., Sonnewald U., Frommer W., Stratmann M., Schell J., Willmitzer L. Both developmental and metabolic signals activate the promoter of a class I patatin gene. EMBO J. 1989 Jan;8(1):23–29. doi: 10.1002/j.1460-2075.1989.tb03344.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rose M., Albig W., Entian K. D. Glucose repression in Saccharomyces cerevisiae is directly associated with hexose phosphorylation by hexokinases PI and PII. Eur J Biochem. 1991 Aug 1;199(3):511–518. doi: 10.1111/j.1432-1033.1991.tb16149.x. [DOI] [PubMed] [Google Scholar]
- Sadka A., DeWald D. B., May G. D., Park W. D., Mullet J. E. Phosphate Modulates Transcription of Soybean VspB and Other Sugar-Inducible Genes. Plant Cell. 1994 May;6(5):737–749. doi: 10.1105/tpc.6.5.737. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sheen J. Metabolic repression of transcription in higher plants. Plant Cell. 1990 Oct;2(10):1027–1038. doi: 10.1105/tpc.2.10.1027. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Takeda S., Mano S., Ohto Ma., Nakamura K. Inhibitors of Protein Phosphatases 1 and 2A Block the Sugar-Inducible Gene Expression in Plants. Plant Physiol. 1994 Oct;106(2):567–574. doi: 10.1104/pp.106.2.567. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Trumbly R. J. Glucose repression in the yeast Saccharomyces cerevisiae. Mol Microbiol. 1992 Jan;6(1):15–21. doi: 10.1111/j.1365-2958.1992.tb00832.x. [DOI] [PubMed] [Google Scholar]
- Yang Y., Kwon H. B., Peng H. P., Shih M. C. Stress responses and metabolic regulation of glyceraldehyde-3-phosphate dehydrogenase genes in Arabidopsis. Plant Physiol. 1993 Jan;101(1):209–216. doi: 10.1104/pp.101.1.209. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yu S. M., Kuo Y. H., Sheu G., Sheu Y. J., Liu L. F. Metabolic derepression of alpha-amylase gene expression in suspension-cultured cells of rice. J Biol Chem. 1991 Nov 5;266(31):21131–21137. [PubMed] [Google Scholar]