Literature DB >> 2696339

Molecular properties and biogenesis of phytochrome I and II.

M Furuya1.   

Abstract

Previously, phytochrome was thought to consist of a single molecular species. However, physiological and spectrophotometric evidence has accumulated to indicate that there are two phytochrome pools in tissues, one of which is predominant in dark-grown tissues and rather unstable in the light, and the other present in very low concentrations but stable, even in the Pfr form, irrespective of light condition. Recently, two immunochemically distinct phytochromes I and II, PI and PII, were found in both dark- and light-grown tissues, and their comparative amino acid sequences shown to be 64% homologous. This is crucial evidence for the presence of chemically different phytochrome apoproteins in a single plant species. However, it is still an open question as to which phytochrome, PI or PII, is a component of the photolabile and photostable pools of phytochrome. Our understanding of the molecular structure of phytochrome has been greatly improved by recent, rapid progress in the cloning and characterization of phytochrome genes. The expression of PI genes is photoreversibly inhibited by the photostable Pfr pool, while that of several other genes, like Cab, appears to be induced by PI in the Pfr form. It is suggested that autoregulation of phytochrome gene expression is not so simply governed in plants as thought earlier. If there are two different phytochromes in a plant cell, the most important physiological problem to be solved is which phytochrome triggers the numerous red/far-red reversible reactions reported in the literature. Photomorphogenetic mutants and transgenic plants with engineered phytochrome genes will probably help to solve this problem in the future, and preliminary work along this line has already introduced in this article. A model of the molecular structure of pea PI dimer was proposed on the basis of small angle X-ray scattering analysis, and the model then confirmed by rotary shadowing electron microscopy. Important questions are still open, such as: what is the nature of phytochrome's partner compounds in cells (phytochrome receptor)? How is/are the phytochrome-induced signal(s) transmitted in the signal transduction chain?

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Year:  1989        PMID: 2696339     DOI: 10.1016/0065-227x(89)90006-3

Source DB:  PubMed          Journal:  Adv Biophys        ISSN: 0065-227X


  35 in total

1.  A plastidic ABC protein involved in intercompartmental communication of light signaling.

Authors:  S G Møller; T Kunkel; N H Chua
Journal:  Genes Dev       Date:  2001-01-01       Impact factor: 11.361

2.  The circadian oscillator is regulated by a very low fluence response of phytochrome in wheat.

Authors:  F Nagy; E Fejes; B Wehmeyer; G Dallman; E Schafer
Journal:  Proc Natl Acad Sci U S A       Date:  1993-07-01       Impact factor: 11.205

3.  Complementation of phytochrome chromophore-deficient Arabidopsis by expression of phycocyanobilin:ferredoxin oxidoreductase.

Authors:  Chitose Kami; Keiko Mukougawa; Takuya Muramoto; Akiho Yokota; Tomoko Shinomura; J Clark Lagarias; Takayuki Kohchi
Journal:  Proc Natl Acad Sci U S A       Date:  2004-01-13       Impact factor: 11.205

4.  Structural domains of phytochrome deduced from homologies in amino acid sequences.

Authors:  M Romanowski; P S Song
Journal:  J Protein Chem       Date:  1992-04

5.  Illuminating Phytochrome Functions (There Is Light at the End of the Tunnel).

Authors:  R. D. Vierstra
Journal:  Plant Physiol       Date:  1993-11       Impact factor: 8.340

6.  Isolation and Initial Characterization of Arabidopsis Mutants That Are Deficient in Phytochrome A.

Authors:  A. Nagatani; J. W. Reed; J. Chory
Journal:  Plant Physiol       Date:  1993-05       Impact factor: 8.340

7.  Phytochrome A and Phytochrome B Have Overlapping but Distinct Functions in Arabidopsis Development.

Authors:  J. W. Reed; A. Nagatani; T. D. Elich; M. Fagan; J. Chory
Journal:  Plant Physiol       Date:  1994-04       Impact factor: 8.340

8.  The Induction of Seed Germination in Arabidopsis thaliana Is Regulated Principally by Phytochrome B and Secondarily by Phytochrome A.

Authors:  T. Shinomura; A. Nagatani; J. Chory; M. Furuya
Journal:  Plant Physiol       Date:  1994-02       Impact factor: 8.340

9.  Photophysiology of the Elongated Internode (ein) Mutant of Brassica rapa: ein Mutant Lacks a Detectable Phytochrome B-Like Polypeptide.

Authors:  P F Devlin; S B Rood; D E Somers; P H Quail; G C Whitelam
Journal:  Plant Physiol       Date:  1992-11       Impact factor: 8.340

10.  Rice type I phytochrome regulates hypocotyl elongation in transgenic tobacco seedlings.

Authors:  A Nagatani; S A Kay; M Deak; N H Chua; M Furuya
Journal:  Proc Natl Acad Sci U S A       Date:  1991-06-15       Impact factor: 11.205

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