Literature DB >> 16662000

Characterization of a molecular modification of phytochrome that is associated with its conversion to the far-red-absorbing form.

M L Boeshore1, L H Pratt.   

Abstract

Phytochrome that has been photoinduced to pellet by irradiation of intact oat (cv. Garry) shoots and recovered from a pellet obtained by centrifugation of crude extracts exhibits modified behavior when compared to soluble phytochrome isolated from shoots that had never been irradiated. This modified behavior includes retarded mobility during sodium dodecyl sulfate polyacrylamide gel electrophoresis (Boeshore ML, LH Pratt 1980 Plant Physiol 66: 500-504). The electrophoretic mobility of several different kinds of phytochrome preparations were examined to study how this modification might arise.Phytochrome that was extracted in the pelletable condition from red-, far-red-irradiated tissue, but without added divalent cation so that it did not pellet, did not exhibit an altered electrophoretic mobility. Hence, this modification of phytochrome is not required for the expression in vitro of pelletability induced in vivo. Phytochrome that was extracted in the pelletable condition and in the far-red-absorbing form, but without added divalent cation so that it did not pellet, and phytochrome in the far-red-absorbing form that remained in the supernatant after collection of pellets containing pelleted phytochrome both electrophoresed with reduced mobility. Thus, this modification does not arise as a consequence of phytochrome having been pelleted. Differential sensitivity of phytochrome to different handling conditions also is not the cause of this modification since the far-red-absorbing form of phytochrome, which was extracted in the pelletable condition but by the same protocol used to extract soluble phytochrome, also exhibited reduced mobility. Furthermore, the reduced electrophoretic rate is not due to a simple differential lability of the far-red-absorbing form of phytochrome to extraction conditions, since partially purified soluble phytochrome that was exposed in the far-red-absorbing form to the isolation and extraction conditions used for preparation of soluble phytochrome did not exhibit the alteration.The data are instead consistent with the more complex interpretation that phytochrome is modified in vitro if two conditions are met: (a) that phytochrome is extracted in the far-red-absorbing form or is converted to the far-red-absorbing form in the crude extract soon after extraction and (b), that phytochrome remains in the far-red-absorbing form in the crude extract for at least a brief period.The possibility that the phytochrome modification studied here might have arisen because of a change in carbohydrate content was tested by periodic acid Schiff staining of sodium dodecyl sulfate polyacrylamide gels. No carbohydrate was detected in any of the phytochrome preparations that were examined. This inability to detect carbohydrate is in direct contrast to the report of Roux et al. (1975 Physiol Plant 35: 85-90).

Entities:  

Year:  1981        PMID: 16662000      PMCID: PMC425987          DOI: 10.1104/pp.68.4.789

Source DB:  PubMed          Journal:  Plant Physiol        ISSN: 0032-0889            Impact factor:   8.340


  10 in total

1.  Irradiation-enhanced Phytochrome Pelletability: Requirement for Phosphorylative Energy in Vivo.

Authors:  P H Quail; W R Briggs
Journal:  Plant Physiol       Date:  1978-11       Impact factor: 8.340

2.  Phytochrome Modification and Light-enhanced, In Vivo-induced Phytochrome Pelletability.

Authors:  M L Boeshore; L H Pratt
Journal:  Plant Physiol       Date:  1980-09       Impact factor: 8.340

3.  Phytochrome immunoaffinity purification.

Authors:  R E Hunt; L H Pratt
Journal:  Plant Physiol       Date:  1979-08       Impact factor: 8.340

4.  On the molecular weight of phytochrome: a new high molecular phytochrome species in oat seedlings.

Authors:  S Grombein; W Rüdiger
Journal:  Hoppe Seylers Z Physiol Chem       Date:  1976-07

5.  Glycoproteins of cell surfaces. A comparative study of three different cell surfaces of the rat.

Authors:  H Glossmann; D M Neville
Journal:  J Biol Chem       Date:  1971-10-25       Impact factor: 5.157

6.  Glycoprotein staining following electrophoresis on acrylamide gels.

Authors:  R M Zacharius; T E Zell; J H Morrison; J J Woodlock
Journal:  Anal Biochem       Date:  1969-07       Impact factor: 3.365

7.  The reliability of molecular weight determinations by dodecyl sulfate-polyacrylamide gel electrophoresis.

Authors:  K Weber; M Osborn
Journal:  J Biol Chem       Date:  1969-08-25       Impact factor: 5.157

8.  Physicochemical differences between the red- and the far-red-absorbing forms of phytochrome.

Authors:  R E Hunt; L H Pratt
Journal:  Biochemistry       Date:  1981-02-17       Impact factor: 3.162

9.  Comparative immunochemistry of phytochrome.

Authors:  L H Pratt
Journal:  Plant Physiol       Date:  1973-01       Impact factor: 8.340

10.  Red Light-enhanced Phytochrome Pelletability: Re-examination and Further Characterization.

Authors:  L H Pratt; D Marmé
Journal:  Plant Physiol       Date:  1976-11       Impact factor: 8.340

  10 in total
  3 in total

1.  The transcript abundance of GmGT-2, a new member of the GT-2 family of transcription factors from soybean, is down-regulated by light in a phytochrome-dependent manner.

Authors:  K O'Grady; V H Goekjian; C J Naim; R T Nagao; J L Key
Journal:  Plant Mol Biol       Date:  2001-10       Impact factor: 4.076

2.  Fruit-localized phytochromes regulate lycopene accumulation independently of ethylene production in tomato.

Authors:  R Alba; M M Cordonnier-Pratt; L H Pratt
Journal:  Plant Physiol       Date:  2000-05       Impact factor: 8.340

3.  Native phytochrome: Inhibition of proteolysis yields a homogeneous monomer of 124 kilodaltons from Avena.

Authors:  R D Vierstra; P H Quail
Journal:  Proc Natl Acad Sci U S A       Date:  1982-09       Impact factor: 11.205

  3 in total

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