Literature DB >> 27520051

The structure and function of phytochrome A: the roles of the entire molecule and of its various parts.

K Manabe1, M Nakazawa2.   

Abstract

Phytochrome A is readily cleavable by proteolytic agents to yield an amino-terminal fragment of 66 kilodalton (kDa), which consists of residues 1 to approximately 600, and a dimer of the carboxy-terminal 55-kDa fragment, from residue 600 or so to the carboxyl terminus. The former domain, carrying the tetrapyrrole chromophore, has been studied extensively because of its photoactivity, while less attention has been paid to the non-chromophoric portion until quite recently. However, the evidence gathered to date suggests that this domain is also of great improtance. We present here a review of the structure and the biochemical and physiological functions of the two domains, of parts of these domains, and of the cooperation between them.

Entities:  

Keywords:  Carboxy-terminal deletion (phytochrome); Domain structure (phytochrome); Photoconversion; Phytochrome; Structure and function (phytochrome); Transgenic plants

Year:  1997        PMID: 27520051     DOI: 10.1007/BF02506850

Source DB:  PubMed          Journal:  J Plant Res        ISSN: 0918-9440            Impact factor:   3.000


  76 in total

1.  Localization of protein-protein interactions between subunits of phytochrome.

Authors:  M D Edgerton; A M Jones
Journal:  Plant Cell       Date:  1992-02       Impact factor: 11.277

2.  Carboxy-terminal deletion analysis of oat phytochrome A reveals the presence of separate domains required for structure and biological activity.

Authors:  J R Cherry; D Hondred; J M Walker; J M Keller; H P Hershey; R D Vierstra
Journal:  Plant Cell       Date:  1993-05       Impact factor: 11.277

3.  Subunit interactions in the carboxy-terminal domain of phytochrome.

Authors:  M D Edgerton; A M Jones
Journal:  Biochemistry       Date:  1993-08-17       Impact factor: 3.162

4.  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

5.  A differential molecualr topography of the Pr and Pfr forms of native oat phytochrome as probed by fluoresence quenching.

Authors:  B R Singh; P S Song
Journal:  Planta       Date:  1990-05       Impact factor: 4.116

6.  Phytochrome-Deficient hy1 and hy2 Long Hypocotyl Mutants of Arabidopsis Are Defective in Phytochrome Chromophore Biosynthesis.

Authors:  B. M. Parks; P. H. Quail
Journal:  Plant Cell       Date:  1991-11       Impact factor: 11.277

7.  Overexpression of Phytochrome B Induces a Short Hypocotyl Phenotype in Transgenic Arabidopsis.

Authors:  D. Wagner; J. M. Tepperman; P. H. Quail
Journal:  Plant Cell       Date:  1991-12       Impact factor: 11.277

8.  Mutations in the gene for the red/far-red light receptor phytochrome B alter cell elongation and physiological responses throughout Arabidopsis development.

Authors:  J W Reed; P Nagpal; D S Poole; M Furuya; J Chory
Journal:  Plant Cell       Date:  1993-02       Impact factor: 11.277

9.  Rice Phytochrome Is Biologically Active in Transgenic Tobacco.

Authors:  S. A. Kay; A. Nagatani; B. Keith; M. Deak; M. Furuya; N. H. Chua
Journal:  Plant Cell       Date:  1989-08       Impact factor: 11.277

10.  Phytochrome A null mutants of Arabidopsis display a wild-type phenotype in white light.

Authors:  G C Whitelam; E Johnson; J Peng; P Carol; M L Anderson; J S Cowl; N P Harberd
Journal:  Plant Cell       Date:  1993-07       Impact factor: 11.277

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