Home LiteratureArticle Details
PMID: 24425162 Published · ppublish English Journal Article

Photoregulation of gene expression in the filamentous cyanobacterium Calothrix sp. PCC 7601: light-harvesting complexes and cell differentiation.

Photosynthesis research ·Vol. 18 ·No. 1-2 ·1988-10-00 ·Pages 99-132

De Marsac NT, Mazel D, Damerval T, Guglielmi G, Capuano V, Houmard J

Abstract

Light plays a major role in many physiological processes in cyanobacteria. In Calothrix sp. PCC 7601, these include the biosynthesis of the components of the light-harvesting antenna (phycobilisomes) and the differentiation of the vegetative trichomes into hormogonia (short chains of smaller cells). In order to study the molecular basis for the photoregulation of gene expression, physiological studies have been coupled with the characterization of genes involved either in the formation of phycobilisomes or in the synthesis of gas vesicles, which are only present at the hormogonial stage.In each system, a number of genes have been isolated and sequenced. This demonstrated the existence of multigene families, as well as of gene products which have not yet been identified biochemically. Further studies have also established the occurrence of both transcriptional and post-transcriptional regulation. The transcription of genes encoding components of the phycobilisome rods is light-wavelength dependent, while translation of the phycocyanin genes may require the synthesis of another gene product irrespective of the light regime. In this report, we propose two hypothetical models which might be part of the complex regulatory mechanisms involved in the formation of functional phycobilisomes. On the other hand, transcription of genes involved in the gas vesicles formation (gvp genes) is turned on during hormogonia differentiation, while that of phycobiliprotein genes is simultaneously turned off. In addition, and antisense RNA which might modulate the translation of the gvp mRNAs is synthezised.

Authors & Affiliations
6 authors, click to expand affiliations / ORCID
De Marsac N T
Unité de Physiologie Microbienne (C.N.R.S., U.A. 1129), Département de Biochimie et Génétique Moléculaire, Institut Pasteur, 28 rue du Docteur Roux, 75724, Paris Cedex 15, France.
Mazel D
Damerval T
Guglielmi G
Capuano V
Houmard J
References (50)
50 references, click to expand
  1. Phycobilisome-associated glycoproteins in the cyanobacterium Anacystis nidulans R 2.
    FEBS Lett. 1987 May 11;215(2):209-14 PMID: 2438157
  2. Construction of shuttle vectors capable of conjugative transfer from Escherichia coli to nitrogen-fixing filamentous cyanobacteria.
    Proc Natl Acad Sci U S A. 1984 Mar;81(5):1561-5 PMID: 6324204
  3. A plasmid-encoded gas vesicle protein gene in a halophilic archaebacterium.
    Mol Microbiol. 1987 Nov;1(3):365-70 PMID: 3448465
  4. Determinants of messenger RNA stability.
    Cell. 1987 Jan 16;48(1):5-6 PMID: 2431794
  5. Differential expression of photosynthesis genes in R. capsulata results from segmental differences in stability within the polycistronic rxcA transcript.
    Cell. 1985 Jan;40(1):171-81 PMID: 2981627
  6. Phototrophic prokaryotes: the cyanobacteria.
    Annu Rev Microbiol. 1977;31:225-74 PMID: 410354
  7. Transcriptional analysis of the cyanobacterial gvpABC operon in differentiated cells: occurrence of an antisense RNA complementary to three overlapping transcripts.
    Gene. 1987;60(1):29-37 PMID: 2450053
  8. Division patterns and cellular differentiation in cyanobacteria.
    Ann Inst Pasteur Microbiol (1985). 1985 Jan-Feb;136A(1):33-9 PMID: 3923902
  9. Transcription termination and the regulation of gene expression.
    Annu Rev Biochem. 1986;55:339-72 PMID: 3527045
  10. Complete nucleotide sequence of the red-light specific set of phycocyanin genes from the cyanobacterium Calothrix PCC 7601.
    Nucleic Acids Res. 1988 Feb 25;16(4):1626 PMID: 3126486
  11. Genes for the alpha and beta subunits of phycocyanin.
    Proc Natl Acad Sci U S A. 1984 Dec;81(24):7946-50 PMID: 6096868
  12. Identification of a positive retroregulator that stabilizes mRNAs in bacteria.
    Proc Natl Acad Sci U S A. 1986 May;83(10):3233-7 PMID: 3085085
  13. Morphological parameters and macromolecular organization of gas vacuole membranes of Microcystis aeruginosa Kuetz. emend. Elenkin.
    Can J Microbiol. 1970 Mar;16(3):159-64 PMID: 4191159
  14. Cyanobacterial light-harvesting complex subunits encoded in two red light-induced transcripts.
    Science. 1985 Nov 1;230(4725):550-3 PMID: 3931221
  15. Isolation and molecular characterization of the gene encoding allophycocyanin B, a terminal energy acceptor in cyanobacterial phycobilisomes.
    Mol Microbiol. 1988 Jan;2(1):101-7 PMID: 3130540
  16. Phycobilisomes: macromolecular structure and energy flow dynamics.
    Biophys J. 1986 Jan;49(1):115-6 PMID: 19431610
  17. The complete amino-acid sequence of both subunits of phycoerythrocyanin from the thermophilic cyanobacterium Mastigocladus laminosus.
    Hoppe Seylers Z Physiol Chem. 1983 Jun;364(6):691-712 PMID: 6411579
  18. Control of phycobiliprotein proteolysis and heterocyst differentiation in Anabaena.
    J Bacteriol. 1980 Mar;141(3):1375-85 PMID: 6767709
  19. Phycobilisomes: structure and dynamics.
    Annu Rev Microbiol. 1982;36:173-98 PMID: 6816134
  20. Genes encoding major light-harvesting polypeptides are clustered on the genome of the cyanobacterium Fremyella diplosiphon.
    Proc Natl Acad Sci U S A. 1986 Jun;83(11):3924-8 PMID: 3086870
  21. Post-translational methylation of asparaginyl residues. Identification of beta-71 gamma-N-methylasparagine in allophycocyanin.
    J Biol Chem. 1986 Dec 5;261(34):15891-4 PMID: 3782095
  22. Occurrence and nature of chromatic adaptation in cyanobacteria.
    J Bacteriol. 1977 Apr;130(1):82-91 PMID: 856789
  23. Regulation of Nostoc sp. phycobilisome structure by light and temperature.
    J Bacteriol. 1983 Sep;155(3):1407-16 PMID: 6411691
  24. Linker polypeptides of the phycobilisome from the cyanobacterium Mastigocladus laminosus: amino-acid sequences and relationships.
    Biol Chem Hoppe Seyler. 1985 Oct;366(10):993-1001 PMID: 3933528
  25. Organization and nucleotide sequence of genes encoding core components of the phycobilisomes from Synechococcus 6301.
    Mol Gen Genet. 1986 Dec;205(3):404-10 PMID: 3031427
  26. Phycocyanin synthesis and degradation in the blue-green bacterium Anacystis nidulans.
    J Bacteriol. 1977 Dec;132(3):771-8 PMID: 924972
  27. Cloning and light regulation of expression of the phycocyanin operon of the cyanobacterium Anabaena.
    EMBO J. 1987 Apr;6(4):871-84 PMID: 3109890
  28. Core substructure in cyanobacterial phycobilisomes.
    J Cell Biochem. 1983;22(1):1-14 PMID: 6421826
  29. Molecular cloning and nucleotide sequence of a developmentally regulated gene from the cyanobacterium Calothrix PCC 7601: a gas vesicle protein gene.
    Nucleic Acids Res. 1985 Oct 25;13(20):7223-36 PMID: 2997744
  30. Role of the colorless polypeptides in phycobilisome reconstitution from separated phycobiliproteins.
    Plant Physiol. 1982 May;69(5):991-7 PMID: 16662378
  31. Secondary structure of the Tetrahymena ribosomal RNA intervening sequence: structural homology with fungal mitochondrial intervening sequences.
    Proc Natl Acad Sci U S A. 1983 Jul;80(13):3903-7 PMID: 6306649
  32. Light harvesting by phycobilisomes.
    Annu Rev Biophys Biophys Chem. 1985;14:47-77 PMID: 3924069
  33. Isolation and characterization of light-regulated phycobilisome linker polypeptide genes and their transcription as a polycistronic mRNA.
    J Bacteriol. 1987 Jun;169(6):2675-84 PMID: 3108238
  34. Gene amplification.
    Annu Rev Biochem. 1984;53:447-91 PMID: 6383198
  35. Light-induced Changes in Allophycocyanin.
    Plant Physiol. 1980 Jan;65(1):6-12 PMID: 16661143
  36. A developmentally regulated gvpABC operon is involved in the formation of gas vesicles in the cyanobacterium Calothrix 7601.
    Gene. 1987;54(1):83-92 PMID: 3111941
  37. Light Intensity Adaptation and Phycobilisome Composition of Microcystis aeruginosa.
    Plant Physiol. 1985 Dec;79(4):983-7 PMID: 16664557
  38. Stabilization of translationally active mRNA by prokaryotic REP sequences.
    Cell. 1987 Jan 30;48(2):297-310 PMID: 2433046
  39. Photoreversible absorbance changes in solutions of allophycocyanin purified from Fremyella diplosiphon: Temperature dependence and quantum efficiency.
    Proc Natl Acad Sci U S A. 1979 Nov;76(11):5655-9 PMID: 16592721
  40. Cloning and sequencing of the genes encoding the alpha and beta subunits of C-phycocyanin from the cyanobacterium Agmenellum quadruplicatum.
    Proc Natl Acad Sci U S A. 1984 Nov;81(22):6983-7 PMID: 6438628
  41. Asymmetrical core structure in phycobilisomes of the cyanobacterium Synechocystis 6701.
    J Mol Biol. 1986 Oct 5;191(3):441-51 PMID: 3102748
  42. Complete amino acid sequence of cyanobacterial gas-vesicle protein indicates a 70-residue molecule that corresponds in size to the crystallographic unit cell.
    Biochem J. 1986 May 15;236(1):31-6 PMID: 3098234
  43. The complete amino-acid sequence of C-phycoerythrin from the cyanobacterium Fremyella diplosiphon.
    Biol Chem Hoppe Seyler. 1986 Jul;367(7):627-42 PMID: 3092842
  44. Green light induces transcription of the phycoerythrin operon in the cyanobacterium Calothrix 7601.
    Nucleic Acids Res. 1986 Nov 11;14(21):8279-90 PMID: 2431391
  45. Control of Phycoerythrin Synthesis during Chromatic Adaptation.
    Plant Physiol. 1979 Nov;64(5):786-90 PMID: 16661054
  46. A multigene family in Calothrix sp. PCC 7601 encodes phycocyanin, the major component of the cyanobacterial light-harvesting antenna
    Mol Gen Genet. ;211(2):296-304 PMID: 28124876
  47. Regulated synthesis of phycobilisome components.
    Photochem Photobiol. 1986 Dec;44(6):827-37 PMID: 3104939
  48. Linker polypeptides of the phycobilisome from the cyanobacterium Mastigocladus laminosus. II. Amino-acid sequences and functions.
    Biol Chem Hoppe Seyler. 1986 Jul;367(7):615-26 PMID: 3092841
  49. Complementary chromatic adaptation in a filamentous blue-green alga.
    J Cell Biol. 1973 Aug;58(2):419-35 PMID: 4199659
  50. Identification of facultatively heterotrophic, N2-fixing cyanobacteria able to receive plasmid vectors from Escherichia coli by conjugation.
    J Bacteriol. 1985 Jun;162(3):1339-41 PMID: 3922953
Article Info
Journal
Photosynthesis research
Abbr.
Photosynth Res
ISSN
0166-8595
Published
1988-10-00
Pages
99-132
Language
English
Region
Netherlands
NLM ID
100954728
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com