Arabidopsis constitutive photomorphogenic mutant, bls1, displays altered brassinosteroid response and sugar sensitivity

Plant Molecular Biology

Volumn 56, Issue 2, 2004, Pages 185-201

  Laxmi, Ashverya ^a   Paul, Laju K ^a   Peters, Janny L ^b   Khurana, Jitendra P ^a  

^a UNIVERSITY OF DELHI   (India)

^b RADBOUD UNIVERSITY NIJMEGEN   (Netherlands)

Author keywords

Arabidopsis; Brassinosteroids; De etiolation; Light hormone interaction; Sugar signalling

Indexed keywords

BIOSYNTHESIS; GENES; HORMONES; MUTAGENESIS;

ARABIDOPSIS; SILIQUE FORMATION; SUGAR SIGNALLING; TRICHOME NUMBERS;

SUGAR (SUCROSE);

ABSCISIC ACID; ARABIDOPSIS PROTEIN; BETA GLUCURONIDASE; BRASSINOLIDE; CARBOHYDRATE; CHOLESTANOL; GIBBERELLIN; GLUCOSE; HETEROCYCLIC STEROID; HYBRID PROTEIN; INDOLEACETIC ACID DERIVATIVE; PHYTOHORMONE; SUCROSE;

ARABIDOPSIS; ARTICLE; CHROMOSOME MAP; COMPARATIVE STUDY; CROSS BREEDING; DARKNESS; DOSE RESPONSE; DRUG EFFECT; GENE EXPRESSION REGULATION; GENETICS; GENOTYPE; GROWTH, DEVELOPMENT AND AGING; LIGHT; METABOLISM; MORPHOGENESIS; MUTATION; PHENOTYPE; PLANT CHROMOSOME; PLANT GROWTH; PLANT ROOT; RADIATION EXPOSURE; TRANSGENIC PLANT;

ABSCISIC ACID; ARABIDOPSIS; ARABIDOPSIS PROTEINS; CARBOHYDRATES; CHOLESTANOLS; CHROMOSOME MAPPING; CHROMOSOMES, PLANT; CROSSES, GENETIC; DARKNESS; DOSE-RESPONSE RELATIONSHIP, DRUG; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GENE EXPRESSION REGULATION, PLANT; GENOTYPE; GIBBERELLINS; GLUCOSE; GLUCURONIDASE; HYPOCOTYL; INDOLEACETIC ACIDS; LIGHT; MORPHOGENESIS; MUTATION; PHENOTYPE; PLANT GROWTH REGULATORS; PLANT ROOTS; PLANTS, GENETICALLY MODIFIED; RECOMBINANT FUSION PROTEINS; STEROIDS, HETEROCYCLIC; SUCROSE;

BIOSYNTHESIS; GENES; HORMONES; MUTAGENS; SUGARS;

ARABIDOPSIS; EMBRYOPHYTA;

EID: 12444315419     PISSN: 01674412     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11103-004-2799-x     Document Type: Article

References (48)

1. Azpiroz, R., Wu, Y., LoCascio, J.C. and Feldmann, K.A. 1998. An Arabidopsis brassinosteroid-dependent mutant is blocked in cell elongation. Plant Cell 10: 219-230.
2. Bancos, S., Nomura, T., Sato, T., Molnar, G., Bishop, G.J., Koncz, C., Yokota, T., Nagy, F. and Szekeres, M. 2002. Regulation of transcript levels of the Arabidopsis cytochrome P 450 genes involved in brassinosteroid biosynthesis. Plant Physiol. 130: 504-513.
3. Bleecker, A., Estelle, M., Somerville, C. and Kende, H. 1988. Insensitivity to ethylene conferred by a dominant mutation in Arabidopsis thaliana. Science 241: 1086-1089.
4. Boerjan, W., Cervera, M-T., Delarue, M., Beckman, T., Dewitte, W., Bellini, C., Caboche, M., Onckelen, H.V. and Inze, D. 1995. superroot, a recessive mutation in Arabidopsis, confers auxin overproduction. Plant Cell 7: 1405-1419.
5. Catterou, M., Dubois, F., Smets, R., Vaniet, S., Kichey, T., Onckelen, H.V., Sangwan-Norreel, B.S. and Sangwan, R.S. 2002. hoc: an Arabidopsis mutant overproducing cytokinins and expressing high in vitro organogenic capacity. Plant J. 30: 273-287.
6. Chaudhury, A.M., Letham, S. and Craig, S. 1993. amp1, a mutant with high cytokinin levels and altered embryonic pattern, faster vegetative growth, constitutive photomorphogenesis and precocious flowering. Plant J. 4: 907-914.
7. Chin-Atkins, A.N., Criag, S., Hocrat, C.H., Denn, E.S. and Chaudhury, A.M. 1996. Increased endogenous cytokinins in the Arabidopsis amp1 mutant corresponds with de-etiolation responses. Planta 198: 549-556.
8. Chory, J., Nagpal, P. and Peto, C.A. 1991. Phenotypic and genetic analysis of det2, a new mutant that affects light-regulated seedling development in Arabidopsis. Plant Cell 3: 445-459.
9. Delarue, M., Prinsen, E., Onckelen, H.V., Caboche, M. and Bellini, C. 1998. sur2 mutations of Arabidopsis thaliana define a new locus involved in the control of auxin homeostasis. Plant J. 14: 603-611.
10. Ephritikhine, G., Fellner, M., Vannini, C., Lapous, D. and Barbier-Brygoo, H. 1999a. The sax1 dwarf mutant of Arabidopsis thaliana shows altered sensitivity of growth responses to abscisic acid, auxin, gibberellins and ethylene and is partially rescued by exogenous brassinosteroids. Plant J. 18: 303-314.
11. Ephritikhine, G., Pagant, S., Fujioka, S., Takatsuto, S., Lapous, D., Caboche, M., Kendrick, R.E. and Barbier-Brygoo, H. 1999b. The sax1 mutation defines a new locus involved in the brassinosteroid biosynthesis pathway in Arabidopsis thaliana. Plant J. 18: 315-320.
12. Feinbaum, R.L. and Ausubel, P.M. 1988. Transcriptional regulation of the Arabidopsis thaliana chalcone synthase gene. Mol. Cell Biol. 8: 1985-1992.
13. Gil, P. and Green, P.J. 1997. Regulatory activity exerted by the SAUR-AC1 promoter region in transgenic plants. Plant Mol. Biol. 34: 803-808.
14. Gil, P., Liu, Y., Orbovic, V., Verkamp, E., Poff, K.L. and Green, P.J. 1994. Characterization of auxin inducible SAUR-AC1 gene for use as a molecular genetic tool in Arabidopsis. Plant Physiol. 104: 777-784.
15. Goda, H., Shimada, Y., Asami, T., Fujioka, S. and Yoshida, S. 2002. Microarray analysis of brassinosteroid-regulated genes in Arabidopsis. Plant Physiol. 130: 1319-1334.
16. Guzman, P. and Ecker, J.R. 1990. Exploiting the triple response of Arabidopsis to identify ethylene-related mutants. Plant Cell 2: 513-523.
17. Kang, J.G., Yun, J., Kim, D.H., Chung, K.S., Fujioka, S., Kim, J.I., Dae, H.W., Yoshida, S.. Takatsuto, S., Song, P.S. and Park, C.M. 2001. Light and brassinosteroid signals are integrated via a dark-induced G protein in etiolated seedling growth. Cell 105: 625-636.
18. Kim, B.C., Soh, M.S., Hong, S.H., Furuya, M. and Nam, H.G. 1998. Photomorphogenic development of the Arabidopsis shy2-1D mutation and its interaction with phytochromes in darkness. Plant J. 15: 61-68.
19. Khurana, J.P., Kochhar, A. and Tyagi, A.K. 1998. Photosensory perception and signal transduction in higher plants - molecular genetic analysis. Crit. Rev. Plant Sci. 17: 465-539.
20. Krishna, P. 2003. Brassinosteroid-mediated stress responses. J. Plant Growth Regul. 22: 289-297.
21. Laby, R.J., Kincaid, M.S., Kim, D. and Gibson, S.I. 2000. The Arabidopsis sugar-insensitive mutants sis4 and sis5 are defective in abscisic acid synthesis and response. Plant J. 23: 587-596.
22. Lehman, A., Black, R. and Ecker, J.R. 1996. HOOKLESS1, an ethylene response gene, is required for differential cell elongation in the Arabidopsis hypocotyl. Cell 85: 183-194.
23. Leon, P. and Sheen, J. 2003. Sugar and hormone connections. Trends Plant Sci. 8: 110-116.
24. Leyser, H.M.O., Lincoln, C., Timpte, C., Lammer, D., Turner, J. and Estelle, M. 1993. The auxin resistance gene AXR1 of Arabidopsis encodes for a protein related to ubiquitin-activating enzyme E1. Nature 364: 161-164.
25. Li, J., Nagpal, P., Vitart, V., McMorris, T.C. and Chory, J. 1996. A role for brassinosteroids in light-dependent development of Arabidopsis. Science 272: 398-401.
26. Li, J., Biswas, M.G., Chao, A., Russell, D.W. and Chory, J. 1997. Conservation of function between mammalian and plant steroid 5α-reductases. Proc. Natl. Acad. Sci. USA 94: 3554-3669.
27. Meinke, D.W., Meinke, L.K., Showalter, T.C., Schissel, A.M., Mueller, L.A. and Tzafrir, I. 2003. A sequence-based map of Arabidopsis genes with mutant phenotypes. Plant Physiol. 131: 409-418.
28. Moore, B., Zhou, L., Rolland, F., Hall, Q., Cheng, W-H., Liu, Y.-X., Hwang, I., Jones, T. and Sheen, J. 2003. Role of Arabidopsis glucose sensor HKX1 in nutrient, light, and hormonal signaling. Science 300: 332-336.
29. Nagpal, P., Walker, L.M., Young, J.C., Sonawala, A., Timpte, C., Estelle, M. and Reed, J.W. 2000. AXR2 encodes a member of Aux/IAA protein family. Plant Physiol. 123: 563-574.
30. Nagy, F., Kay, S.A. and Chua, N-H. 1988. Analysis of gene expression in transgenic plants. In: S.B. Gelvin, R.A. Schilperoort and D.P.S. Verma (Eds.), Plant Molecular Biology Manual. Kluwer Academic Publishers, Dordrecht, pp. B4/1-B4/29.
31. Nakamura, A., Higuchi, K., Goda, H., Fujiwara, M.T., Sawa, S., Koshiba, T., Shimada, Y. and Yoshida, S. 2003a. Brassinolide induces IAA5, IAA19, and DR5, a synthetic auxin response element in Arabidopsis, implying a cross talk point of brassinosteroid and auxin signaling. Plant Physiol. 133: 1843-1853.
32. Nakamura, A., Shimada, Y., Goda, H., Fujiwara M.T., Asami, T. and Yoshida, S. 2003b. AXR1 is involved in BR-mediated elongation and SAUR-AC1 gene expression in Arabidopsis. FEBS Lett. 553: 28-32.
33. Neff, M.M., Fankhauser, C. and Chory, J. 2000. Light: an indicator of time and space. Genes Dev. 14: 257-271.
34. Nemeth, K., Salchert, K., Putnoky, P., Bhalerao, R., Koncz-Kalman, Z., Stankovic-Stangeland, B., Bako, L., Mathur, J., Okresz, L., Stabel, S., Geigenberger, P., Stit, M., Redei, G.P., Schell, J. and Koncz, C. 1998. Pleiotropic control of glucose and hormone responses by PRL1, a nuclear WD protein, in Arabidopsis. Genes Dev. 12: 3059-3073.
35. Perez-Perez, J.M., Ponce, M.R. and Micol, J.L. 2004. The ULTRACURVATA2 gene of Arabidopsis encodes an FK506-binding protein involved in auxin and brassinosteroid signaling. Plant Physiol. 134: 101-117.
36. Peters, J.L., Cnops, G., Neyt, P., Zethof, J., Cornelis, K., Lijsebettens, M.V. and Gerats, T. 2003a. An AFLP-based genome-wide mapping strategy. Theor. Appl. Gen. 108: 321-327.
37. Peters, J.L., Cnudde, F. and Gerats, T. 2003b. Forward genetics and map-based cloning approaches. Trends Plant Sci. 8: 484-491.
38. Peters, J.L., Constandt, H., Neyt, P., Cnops, G., Zethof, J., Zabeau, M. and Gerats, T. 2001. A physical amplified-fragment length polymorphism map of Arabidopsis. Plant Physiol. 127: 1579-1589.
39. Rohde, A., De Rycke, R., Beeckman, T., Engler, G., Van Montagu, M. and Boerjan, W. 2000. ABI3 affects plastid differentiation in dark-grown Arabidopsis seedlings. Plant Cell 12: 35-52.
40. Roldan, M.C., Gomez-Mena, C., Ruiz-Garcia, L., Salinas, J. and Martinez-Zapter J.M. 1999. Sucrose availability on the aerial part of the plant promotes morphogenesis and flowering of Arabidopsis in the dark. Plant J. 20: 581-590.
41. Sakurai, A. and Fujioka, S. 1993. The current status of physiology and biochemistry of brassinosteroids. Plant Growth Reg. 13: 147-159.
42. Somerville, C.R. and Ogren, W.L. 1982. Isolation of photorespiration mutants in Arabidopsis thaliana. In: M. Edelman, R. Hallick and N.-H. Chua, (Eds.), Methods in Chloroplast Molecular Biology. Elsevier, Amsterdam, pp. 129-139.
43. Szekeres, M., Nemeth, K., Koncz-Kalman, Z., Mathur, J., Kauschmann, A., Altmann, T., Redei, G.P., Nagy, F., Schell, J. and Koncz, C. 1996. Brassinosteroids rescue the deficiency of CYP90, a cytochrome P450, controlling cell elongation and de-etiolation in Arabidopsis. Cell 85: 171-182.
44. Takahashi, T., Gasch, A., Nishizawa, N. and Chua, N.-H. 1995. The DIMINUTO gene of Arabidopsis is involved in regulating cell elongation. Genes Dev. 9: 97-107.
45. Tian, Q. and Reed, W.J. 1999. Control of auxin regulated root development by the Arabidopsis thaliana SHY2/IAA3 gene. Development 126: 711-721.
46. Wellburn, A.R. and Lichtenthaler, H. 1984. Formulae and program to determine total carotenoids and chlorophylls A and B of leaf extracts in different solvents. In: C. Sybesma (Ed.), Advances in Photosynthesis Research, vol. II. Martinus Nijhoff/Dr. W. Junk Publishers, pp. 11.1/9-12.
47. Xu, W., Purugganan, M.M., Polisensky, D.H., Antosiewicz, D.M., Fry, S.C. and Bramm, J. 1995. Arabidopsis TCH4, regulated by hormones and the environment, encodes a xyloglucan endotransglycosylate. Plant Cell 7: 1555-1567.
48. Zhou, L., Jang, J.-C., Jones, T.L. and Sheen, J. 1998. Glucose and ethylene signal transduction crosstalk revealed by an Arabidopsis glucose-insensitive mutant. Proc. Natl. Acad. Sci. USA 95: 10294-10299.