Literature DB >> 11539322

Phytochrome is required for the occurrence of time-dependent phototropism in maize coleoptiles

Y J Liu1, M Iino.   

Abstract

Time-dependent phototropism (TDP), sometimes called second positive curvature, occurs when the duration of phototropic stimulation with blue light (B) exceeds a few minutes. TDP was characterized in maize (Zea mays L.) coleoptiles raised under continuous red light (R). Subsequently, coleoptiles adapted to darkness were used to investigate the effect of R on TDP. It was found that TDP, which is induced in R-grown coleoptiles, does not occur in dark-adapted coleoptiles and that dark-adapted coleoptiles begin to show TDP after treatment with R. The TDP responsiveness became maximal 1-2 h after treatment with a R pulse and decreased during the next few hours. At least 10 min was required after a short pulse of R before the coleoptile began to respond to B for the induction of TDP. The effect of R in establishing the TDP responsiveness was totally suppressed by a pulse of far-red light given immediately after an inductive pulse of R. It is concluded that the mechanism of TDP requires for its establishment a R signal perceived by phytochrome. The TDP of R-grown and R-pretreated coleoptiles showed relationships to stimulation times and fluence rates that are similar to those reported for oat coleoptiles, except that TDP of maize showed a sharp increase in its magnitude within a narrow range of stimulation times as short as 5-10 min.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 11539322     DOI: 10.1111/j.1365-3040.1996.tb00016.x

Source DB:  PubMed          Journal:  Plant Cell Environ        ISSN: 0140-7791            Impact factor:   7.228


  9 in total

1.  Phototropism: mechanism and outcomes.

Authors:  Ullas V Pedmale; R Brandon Celaya; Emmanuel Liscum
Journal:  Arabidopsis Book       Date:  2010-08-31

2.  The Rice COLEOPTILE PHOTOTROPISM1 gene encoding an ortholog of Arabidopsis NPH3 is required for phototropism of coleoptiles and lateral translocation of auxin.

Authors:  Ken Haga; Makoto Takano; Ralf Neumann; Moritoshi Iino
Journal:  Plant Cell       Date:  2004-12-14       Impact factor: 11.277

3.  The enhancement of phototropin-induced phototropic curvature in Arabidopsis occurs via a photoreversible phytochrome A-dependent modulation of auxin responsiveness.

Authors:  E L Stowe-Evans; D R Luesse; E Liscum
Journal:  Plant Physiol       Date:  2001-06       Impact factor: 8.340

4.  Phototropism of rice (Oryza sativa L.) coleoptiles: fluence-response relationships, kinetics and photogravitropic equilibrium.

Authors:  R Neumann; M Iino
Journal:  Planta       Date:  1997-03       Impact factor: 4.116

5.  Interaction of cryptochrome 1, phytochrome, and ion fluxes in blue-light-induced shrinking of Arabidopsis hypocotyl protoplasts.

Authors:  X Wang; M Iino
Journal:  Plant Physiol       Date:  1998-08       Impact factor: 8.340

6.  High pigment1 mutation negatively regulates phototropic signal transduction in tomato seedlings.

Authors:  Ankanagari Srinivas; Rajendra K Behera; Takatoshi Kagawa; Masamitsu Wada; Rameshwar Sharma
Journal:  Plant Physiol       Date:  2004-01-22       Impact factor: 8.340

7.  Blue light regulates an auxin-induced K+-channel gene in the maize coleoptile.

Authors:  I Fuchs; K Philippar; K Ljung; G Sandberg; R Hedrich
Journal:  Proc Natl Acad Sci U S A       Date:  2003-09-19       Impact factor: 11.205

8.  PINOID AGC kinases are necessary for phytochrome-mediated enhancement of hypocotyl phototropism in Arabidopsis.

Authors:  Ken Haga; Ken-ichiro Hayashi; Tatsuya Sakai
Journal:  Plant Physiol       Date:  2014-10-03       Impact factor: 8.340

9.  NPH3- and PGP-like genes are exclusively expressed in the apical tip region essential for blue-light perception and lateral auxin transport in maize coleoptiles.

Authors:  Satomi Matsuda; Tomomi Kajizuka; Akeo Kadota; Takeshi Nishimura; Tomokazu Koshiba
Journal:  J Exp Bot       Date:  2011-03-31       Impact factor: 6.992

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.