Literature DB >> 27520054

Photocontrol of anthocyanin biosynthesis in tomato.

L Huub1, J Kerckhoffs1, R E Kendrick2,3.   

Abstract

Juvenile anthocyanin biosynthesis has been studied in dark-grown seedlings of tomato (Lycopersicon esculentum Mill.) wild types (WTs) and photomorphogenic mutants. During a subsequent 24-hr period of monochromatic irradiation at different fluence rates of red light (R) the fluence-rate response relationships for induction of anthocyanin in all the WTs are similar, yet complex, showing a response at low fluence rates (LFRR) followed by a fluence rate-dependent high irradiance response (HIR). In the hypocotyl this response is restricted to the sub-epidermal layer of cells. The high-pigment-1 (hp-1) mutant exhibits a strong amplification of both response components. Theatroviolacea (atv) mutant shows strongest amplification of the HIR component. In contrast, a transgenic line overexpressing an oat phytochrome A gene (PHYA3 (+)) shows a most dramatic amplification of the LFRR component. The far-red light (FR)-insensitive (fri) mutant, deficient in phytochrome A (phyA), lacks the LFRR component whilst retaining a normal HIR. The temporarily R-insensitive (tri) mutant, deficient in phytochrome B1 (phyB1) retains the LFRR, but lacks the HIR. Thehp-1,fri andhp-1,tri double mutant, exhibit amplified, yet qualitatively similar responses to the monogenicfri andtri mutants. Thefri,tri double mutant lacks both response components in R, but a residual response to blue light (B) remains. Similarly, theaurea (au) mutant deficient in phytochrome chromophore biosynthesis and presumably all phytochromes, lacks both response components in the R and FR regions of the spectrum. Experiments at other wavelengths demonstrate that while there is only a small response in the FR spectral region (729 nm) in tomato, there is an appreciable HIR response in the near FR at 704 nm, which is retained in thetri mutant. This suggests that the labile phyA pool participates in the HIR at this wavelength. The intense pigmentation (Ip) mutant appears to be specifically deficient in the B1 induced anthocyanin biosynthesis. Adult plants, grown under fluorescent light/dark cycles, show a reduction of anthocyanin content of young developing leaves upon application of supplemtary or end-of-day FR. The involvement of different phytochrome species in anthocyanin biosynthesis based on micro-injection studies into theau mutant and studies using type specific phytochrome mutants is discussed.

Entities:  

Keywords:  Anthocyanin; Photomorphogenesis; Photomorphogenic mutants; Tomato (Lycopersicon esculentum Mill.)

Year:  1997        PMID: 27520054     DOI: 10.1007/BF02506853

Source DB:  PubMed          Journal:  J Plant Res        ISSN: 0918-9440            Impact factor:   2.629


  17 in total

1.  Oat Phytochrome Is Biologically Active in Transgenic Tomatoes.

Authors:  M. T. Boylan; P. H. Quail
Journal:  Plant Cell       Date:  1989-08       Impact factor: 11.277

2.  Light-grown plants of transgenic tobacco expressing an introduced oat phytochrome A gene under the control of a constitutive viral promoter exhibit persistent growth inhibition by far-red light.

Authors:  A McCormac; G Whitelam; H Smith
Journal:  Planta       Date:  1992-09       Impact factor: 4.116

3.  Functional analysis of yeast-derived phytochrome A and B phycocyanobilin adducts.

Authors:  T Kunkel; G Neuhaus; A Batschauer; N H Chua; E Schäfer
Journal:  Plant J       Date:  1996-10       Impact factor: 6.417

Review 4.  Phytochromes: photosensory perception and signal transduction.

Authors:  P H Quail; M T Boylan; B M Parks; T W Short; Y Xu; D Wagner
Journal:  Science       Date:  1995-05-05       Impact factor: 47.728

5.  The phytochrome gene family in tomato includes a novel subfamily.

Authors:  B A Hauser; M M Cordonnier-Pratt; F Daniel-Vedele; L H Pratt
Journal:  Plant Mol Biol       Date:  1995-12       Impact factor: 4.076

6.  Far-red light-insensitive, phytochrome A-deficient mutants of tomato.

Authors:  A van Tuinen; L H Kerckhoffs; A Nagatani; R E Kendrick; M Koornneef
Journal:  Mol Gen Genet       Date:  1995-01-20

Review 7.  Emerging themes of plant signal transduction.

Authors:  C Bowler; N H Chua
Journal:  Plant Cell       Date:  1994-11       Impact factor: 11.277

8.  Phytochrome signal transduction pathways are regulated by reciprocal control mechanisms.

Authors:  C Bowler; H Yamagata; G Neuhaus; N H Chua
Journal:  Genes Dev       Date:  1994-09-15       Impact factor: 11.361

9.  The mapping of phytochrome genes and photomorphogenic mutants of tomato.

Authors:  A van Tuinen; M Koornneef; M M Cordonnier-Pratt; L H Pratt; R Verkerk; P Zabel
Journal:  Theor Appl Genet       Date:  1997-01       Impact factor: 5.699

10.  Cyclic GMP and calcium mediate phytochrome phototransduction.

Authors:  C Bowler; G Neuhaus; H Yamagata; N H Chua
Journal:  Cell       Date:  1994-04-08       Impact factor: 41.582

View more
  3 in total

1.  Biliverdin reductase-induced phytochrome chromophore deficiency in transgenic tobacco.

Authors:  B L Montgomery; K A Franklin; M J Terry; B Thomas; S D Jackson; M W Crepeau; J C Lagarias
Journal:  Plant Physiol       Date:  2001-01       Impact factor: 8.340

2.  Cyclic GMP acts as a common regulator for the transcriptional activation of the flavonoid biosynthetic pathway in soybean.

Authors:  Kenji Suita; Takaaki Kiryu; Maki Sawada; Maiko Mitsui; Masataka Nakagawa; Kengo Kanamaru; Hiroshi Yamagata
Journal:  Planta       Date:  2008-11-06       Impact factor: 4.116

3.  The tomato homolog of the gene encoding UV-damaged DNA binding protein 1 (DDB1) underlined as the gene that causes the high pigment-1 mutant phenotype.

Authors:  Michal Lieberman; Orit Segev; Nehama Gilboa; Avraham Lalazar; Ilan Levin
Journal:  Theor Appl Genet       Date:  2004-02-14       Impact factor: 5.699

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.