Plant Physiol. Journal of Pharmacology and Experimental Therapeutics
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Plant Physiology 96:775-785 (1991)
© 1991 American Society of Plant Biologists

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Development and Growth Regulation

Characterization of Tobacco Expressing Functional Oat Phytochrome 1

Domains Responsible for the Rapid Degradation of Pfr Are Conserved between Monocots and Dicots

Joel R. Cherry, Howard P. Hershey and Richard D. Vierstra

Department of Horticulture, University of Wisconsin-Madison, Madison, Wisconsin 53706, Agricultural Products Department, E. I. du Pont de Nemours & Co., Wilmington, Delaware 19880-0402

Constitutive expression of a chimeric oat phytochrome gene in tobacco (Nicotiana tabacum) results in the accumulation of a functional 124-kilodalton photoreceptor that markedly alters the phenotype of light-grown tobacco (Keller et al. [1989] EMBO J 8: 1005-1012). Here, we provide a detailed phenotypic and biochemical characterization of homozygous tobacco expressing high levels of oat phytochrome. Phenotypic changes include a substantial inhibition of stem elongation, decreased apical dominance, increased leaf chlorophyll content, and delayed leaf senescence. Oat phytochrome synthesized in tobacco is indistinguishable from that present in etiolated oats, having photoreversible difference spectrum maxima at 665 and 730 nanometers, exhibiting negligible dark reversion of phytochrome—far red-absorbing form (Pfr) to phytochrome—red-absorbing form (Pr), and existing as a dimer with an apparent size of approximately 300 kilodaltons. Heterodimers between the oat and tobacco chromoproteins were detected. Endogenous tobacco phytochrome and transgenically expressed oat phytochrome are rapidly degraded in vivo upon photoconversion of Pr to Pfr. Breakdown of both oat and tobacco Pfr is associated with the accumulation of ubiquitin-phytochrome conjugates, suggesting that degradation occurs via the ubiquitin-dependent proteolytic pathway. This result indicates that the factors responsible for selective recognition of Pfr by the ubiquitin pathway are conserved between monocot and dicot phytochromes. More broadly, it demonstrates that the domain(s) within a plant protein responsible for its selective breakdown can be recognized by the degradation machinery of heterologous species.


1 Supported by grants from the U.S. Department of Energy (DE-F602-88ER13968) and the Research Division of the University of Washington, College Agriculture and Life Sciences (Hatch 2858), to R.D.V. and E.I. du Pont de Nemours & Co.




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Copyright © 1991 by the American Society of Plant Biologists