Etioplast differentiation in Arabidopsis: Both PORA and PORB restore the prolamellar body and photoactive protochlorophyllide-F655 to the cop1 photomorphogenic mutant

Plant Cell

Volumn 10, Issue 2, 1998, Pages 283-296

  Sperling, Ulrich ^a   Franck, Fabrice ^b   Van Cleve, Barbara ^a   Frick, Geneviève ^a   Apel, Klaus ^a   Armstrong, Gregory A ^a  

^a ETH ZURICH   (Switzerland)

^b UNIVERSITY OF LIÈGE   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

ARABIDOPSIS;

EID: 0032004065     PISSN: 10404651     EISSN: None     Source Type: Journal    
DOI: 10.1105/tpc.10.2.283     Document Type: Article

References (56)

1. Apel, K. (1981). The protochlorophyllide holochrome of barley (Hordeum vulgare L.): Phytochrome-induced decrease of translatable mRNA coding for the NADPH:protochlorophyllide oxidoreductase. Eur. J. Biochem. 120, 89-93.
2. Apel, K., Santel, J.-J., Redlinger, T.E., and Falk, H. (1980). The protochlorophyllide holochrome of barley (Hordeum vulgare L): Isolation and characterization of the NADPH-protochlorophyllide oxidoreductase. Eur. J. Biochem. 111, 251-258.
3. Armstrong, G.A., Runge, S., Frick, G., Sperling, U., and Apel, K. (1995). Identification of NADPH:protochlorophyllide oxidoreductases A and B: A branched pathway for light-dependent chlorophyll biosynthesis in Arabidopsis thaliana. Plant Physiol. 108, 1505-1517.
4. Barnes, S.A., Nishizawa, N.K., Quaggio, R.B., Whitelam, G.C., and Chua, N.-H. (1996). Far-red light blocks greening of Arabidopsis seedlings via a phytochrome A - mediated change in plastid development. Plant Cell 8, 601-615.
5. Beale, S.I., and Weinstein, J.D. (1991). Biosynthesis of 5-aminole-vulinic acid in phototrophic organisms. In Chlorophylls, H. Scheer, ed (Boca Raton, FL: CRC Press), pp. 385-406.
6. Böddi, B., Ryberg, M., and Sundqvist, C. (1992). Identification of four universal protochlorophyllide forms in dark-grown leaves by analyses of the 77 K fluorescence emission spectra. J. Photochem. Photobiol. B Biol. 12, 389-401.
7. Brouers, M., and Michel-Wolwertz, M.-R. (1983). Estimation of protochlorophyll(ide) contents in plant extracts; re-evaluation of the molar absorption coefficient of protochlorophyll(ide). Photosynth. Res. 4, 265-270.
8. Butler, W.L., and Briggs, W.R. (1966). The relation between structure and pigments during the first stages of proplastid greening. Biochim. Biophys. Acta 112, 45-53.
9. Castle, L.A., and Meinke, D.W. (1994). A FUSCA gene of Arabidopsis encodes a novel protein essential for plant development. Plant Cell 6, 25-41.
10. Chory, J., Peto, C., Feinbaum, R., Pratt, L., and Ausubel, F. (1989). Arabidopsis thaliana mutant that develops as a light-grown plant in the absence of light. Cell 58, 991-999.
11. Chory, J., Reinecke, D., Sim, S., Washburn, T., and Brenner, M. (1994). A role for cytokinins in de-etiolation in Arabidopsis. Plant Physiol. 104, 339-347.
12. Dehesh, K., and Ryberg, M. (1985). The NADPH-protochlorophyllide oxidoreductase is the major protein constituent of prolamellar bodies in wheat (Triticum aestivum L). Planta 164, 396-399.
13. Deng, X.-W., Caspar, T., and Quail, P.H. (1991). cop1: A regulatory locus involved in light-controlled development and gene expression in Arabidopsis. Genes Dev. 5, 1172-1182.
14. β homologous domain. Cell 71, 791-801.
15. Forreiter, C., and Apel, K. (1993). Light-independent and light-dependent protochlorophyllide-reducing activities and two distinct NADPH-protochlorophyllide oxidoreductase polypeptides in mountain pine (Pinus mugo). Planta 190, 536-545.
16. Frances, S., White, M.J., Edgerton, M.D., Jones, A.M., Elliot, R.C., and Thompson, W.F. (1992). Initial characterization of a pea mutant with light-independent photomorphogenesis. Plant Cell 4, 1519-1530.
17. Franck, F., and Mathis, P. (1980). A short-lived intermediate in the photoenzymatic reduction of protochlorophyll(ide) into chlorophyll(ide) at a physiological temperature. Photochem. Photobiol. 32, 799-803.
18. Franck, F., and Strzalka, K. (1992). Detection of the photoactive protochlorophyllide-protein complex in the light during the greening of barley. FEBS Lett. 309, 73-77.
19. Frick, G., Apel, K., and Armstrong, G.A. (1995). Light-dependent protochlorophyllide oxidoreductase, phytochrome, and greening in Arabidopsis thaliana. In Photosynthesis: From Light to Biosphere, Vol. 3, P. Mathis, ed (Dordrecht, The Netherlands: Kluwer Academic Publishers), pp. 893-898.
20. Fujita, Y. (1996). Protochlorophyllide reduction: A key step in the greening of plants. Plant Cell Physiol. 37, 411-421.
21. Griffiths, W.T. (1978). Reconstitution of chlorophyllide formation by isolated etioplast membranes. Biochem. J. 174, 681-692.
22. Henningsen, K.W., Boynton, J.E., and von Wettstein, D. (1993). Mutants at xantha and albina loci in relation to chloroplast biogenesis in barley (Hordeum vulgare L.). R. Dan. Acad. Sci. Lett. Biol. Skrifter 42, 1-349.
23. Holtorf, H., Reinbothe, S., Reinbothe, C., Bereza, B., and Apel, K. (1995). Two routes of chlorophyllide synthesis that are differentially regulated by light in barley (Hordeum vulgare L.). Proc. Natl. Acad. Sci. USA 92, 3254-3258.
24. Ignatov, N.V., Krasnovskii, A.A., Jr., Litvin, F.F., Belyaeva, O.B., and Walter, G. (1983). Low-temperature (77 K) excitation spectra of fluorescence and phosphorescence of native forms of protochlorophyll(ide) in etiolated leaves of Phaseolus vulgaris and P. coccineus. Photosynthetica 17, 352-360.
25. Kahn, A., Boardman, N.K., and Thorne, S.W. (1970). Energy transfer between protochlorophyllide molecules: Evidence for multiple chromophores in the photoactive protochlorophyllide-protein complex in vivo and in vitro. J. Mol. Biol. 48, 85-101.
26. Kay, S.A., and Griffiths, W.T. (1983). Light-induced breakdown of NADPH-protochlorophyllide oxidoreductase in vitro. Plant Physiol. 72, 229-236.
27. Kirk, J.T.O., and Tilney-Bassett, R.A.E. (1978). The Plastids. (Amsterdam: Elsevier/North-Holland Biomedical Press).
28. Klein, S., and Schiff, J.A. (1972). The correlated appearance of prolamellar bodies, protochlorophyll(ide) species, and the Shibata shift during development of bean etioplasts in the dark. Plant Physiol. 49, 619-626.
29. Lebedev, N., van Cleve, B., Armstrong, G., and Apel., K. (1995). Chlorophyll synthesis in a deetiolated (det340) mutant of Arabidopsis without NADPH-protochlorophyllide (PChlide) oxidoreductase (POR) A and photoactive PChlide-F655. Plant Cell 7, 2081-2090.
30. Li, J., and Timko, M.P. (1996). The pc-1 phenotype of Chlamydomonas reinhardtii results from a deletion mutation in the nuclear gene for NADPH:protochlorophyllide oxidoreductase. Plant Mol. Biol. 30, 15-37.
31. Mariani, P., De Carli, M.E., Rascio, N., Baldan, B., Casadoro, G., Gennari, G., Bodner, M., and Larcher, W. (1990). Synthesis of chlorophyll and photosynthetic competence in etiolated and greening seedlings of Larix decidua as compared with Picea abies. J. Plant Physiol. 137, 5-14.
32. McNellis, T.W., and Deng, X.-W. (1995). Light control of seedling morphogenetic pattern. Plant Cell 7, 1749-1761.
33. McNellis, T.W., von Arnim, A.G., Araki, T., Komeda, Y., Misera, S., and Deng, X.-W. (1994). Genetic and molecular analysis of an allelic series of cop1 mutants suggests functional roles for the multiple protein domains. Plant Cell 6, 487-500.
34. Misera, S., Muller, A.J., Weiland-Heidecker, U., and Jurgens, G. (1994). The FUSCA genes of Arabidopsis: Negative regulators of light responses. Mol. Gen. Genet. 244, 242-252.
35. Oliver, R.P., and Griffiths, W.T. (1982). Pigment-protein complexes of illuminated etiolated leaves. Plant Physiol. 70, 1019-1025.
36. Porta, R.J. (1997). Recent progress in porphyrin and chlorophyll biosynthesis. Photochem. Photobiol. 65, 492-516.
37. Reinbothe, S., Reinbothe, C., Holtorf, H., and Apel, K. (1995). Two NADPH:protochlorophyllide oxidoreductases in barley: Evidence for the selective disappearance of PORA during the light-induced greening of etiolated seedlings. Plant Cell 7, 1933-1940.
38. Reinbothe, S., Reinbothe, C., Lebedev, N., and Apel, K. (1996). PORA and PORB, two light-dependent protochlorophyllide-reducing enzymes of angiosperm chlorophyll biosynthesis. Plant Cell 8, 763-769.
39. Runge, S., van Cleve, B., Lebedev, N., Armstrong, G., and Apel, K. (1995). Isolation and characterization of chlorophyll-deficient xantha mutants of Arabidopsis thaliana. Planta 197, 490-500.
40. Runge, S., Sperling, U., Frick, G., Apel., K., and Armstrong, G.A. (1996). Distinct roles for light-dependent NADPH:protochlorophyllide oxidoreductases (POR) A and B during greening in higher plants. Plant J. 9, 513-523.
41. Ryberg, M., and Dehesh, K. (1986). Localization of NADPH-protochlorophyllide oxidoreductase in dark-grown wheat (Triticum aestivum] by immuno-electron microscopy before and after transformation of the prolamellar bodies. Physiol. Plant. 66, 616-624.
42. Ryberg, M., and Sundqvist, C. (1982). Characterization of prolamellar bodies and prothylakoids fractionated from wheat etioplasts. Physiol. Plant. 56, 125-132.
43. Ryberg, M., and Sundqvist, C. (1988). The regular ultrastructure of isolated prolamellar bodies depends on the presence of membrane-bound NADPH-protochlorophyllide oxidoreductase. Physiol. Plant. 73, 218-226.
44. Santel, H.-J., and Apel, K. (1981). The protochlorophyllide holochrome of barley (Hordeum vulgare L.): The effect of light on the NADPH:protochlorophyllide oxidoreductase. Eur. J. Biochem. 120, 95-103.
45. Selstam, E., and Widell, A. (1986). Characterization of prolamellar bodies, from dark-grown seedlings of Scots pine, containing light-and NADPH-dependent protochlorophyllide oxidoreductase. Physiol. Plant. 67, 345-352.
46. 688-676 phototransformation. Photosynthetica 4, 38-47.
47. Smith, J.H.C., and Benitez, A. (1954). The effect of temperature on the conversion of protochlorophyll to chlorophyll a in etiolated barley leaves. Plant Physiol. 29, 135-143.
48. Spano, A.J., He, Z.-H., and Timko, M.P. (1992). NADPH:protochlorophyllide oxidoreductases in white pine (Pinus strobus) and loblolly pine (P. taeda). Mol. Gen. Genet. 236, 86-95.
49. Sperling, U., van Cleve, B., Frick, G., Apel., K., and Armstrong, G.A. (1997). Overexpression of light-dependent PORA or PORB in plants depleted of endogenous POR by far-red light enhances seedling survival in white light and protects against photooxidative damage. Plant J. 12, 649-658.
50. Sundqvist, C., and Dahlin, C. (1997). With chlorophyll pigments from prolamellar bodies to light-harvesting complexes. Physiol. Plant. 100, 748-759.
51. Sundqvist, C., Seyyedi, M., and Timko, M.P. (1995). Chlorophyll formation in the Lip1 mutant of pea. In Photosynthesis: From Light to Biosphere, Vol. 3, P. Mathis, ed (Dordrecht, The Netherlands: Kluwer Academic Publishers), pp. 1005-1008.
52. Suzuki, J.Y., and Bauer, C.E. (1995). A prokaryotic origin for light-dependent chlorophyll biosynthesis of plants. Proc. Natl. Acad. Sci. USA 92, 3749-3753.
53. von Arnim, A., and Deng, X.-W. (1996) Light control of seedling development. Annu. Rev. Plant Physiol. Plant Mol. Biol. 47, 215-243.
54. von Wettstein, D., Gough, S., and Kannangara, C.G. (1995). Chlorophyll biosynthesis. Plant Cell 7, 1039-1057.
55. Wei, N., and Deng, X.-W. (1992). COP9: A new genetic locus involved in light-regulated development and gene expression in Arabidopsis. Plant Cell 4, 1507-1518.
56. Wei, N., Kwok, S.F., von Arnim, A.G., Lee, A., McNellis, T.W., Peikos, B., and Deng, X.-W. (1994). Arabidopsis COP8, COP10, and COP11 genes are involved in repression of photomorphogenic development in darkness. Plant Cell 6, 629-643.