Phytochrome Responses to End-of-Day Irradiations in Light-grown Corn Grown in the Presence and Absence of Sandoz 9789

Corn seedlings were grown in white light in the absence and presence of the chlorosis-inducing herbicide San 9789. The resulting green and achlorophyllous seedlings were used to investigate phytochrome-mediated responses to end-of-day far red irradiation and reversal of these responses by subsequent red irradiation. Mesocotyl and coleoptile elongation increased in response to end-of-day far red irradiation, whereas the anthocyanin content of the coleoptiles was decreased. All three responses were reversible by red irradiation following the far red. Dose-response curves for far red induction and red reversal of these responses did not differ significantly for plants grown in the presence or absence of San 9789. Thus, San 9789 appears to affect neither phytochrome itself nor the response system involved. Chlorophyll screening likewise does not affect phytochrome relationships for these responses.     

Phytochrome Effects on the Relationship between Chlorophyll and Steady-State Levels of Thylakoid Polypeptides in Light-Grown Tobacco

The effects of phytochrome status on chlorophyll content and on steady-state levels of thylakoid proteins were investigated in green leaves of Nicotiana tabacum L. plants grown under white light. Far-red light given either as a pulse at the end of each photoperiod, or as a supplement to white light during the photoperiod, reduced chlorophyll content per unit area and per unit dry weight. These differences were also observed after resolving chlorophyll-containing polypeptides by gel electrophoresis. Chlorophyll a:b ratio was unchanged. Both Coomassie blue-stained gels and immunochemical analyses showed that, in contrast to the observations in etiolated barley (K Apel, K Kloppstech [1980] Planta 150: 426-430) and pea (J Bennett [1981] Eur J Biochem 118: 61-70) seedlings, and in etiolated tobacco leaves (this report), in fully deetiolated tobacco plants changes in chlorophyll content were not correlated with obvious changes in the steady-state levels of thylakoid proteins (e.g. light-harvesting, chlorophyll a/b-binding proteins).     

Phytochrome changes correlated to mesocotyl inhibition in etiolated Avena seedlings

The elongation of etiolated Avena mesocotyls is inhibited by red light (660 mμ). Immediately after exposing mesocotyl sections to varying doses of red light the ensuing concentrations of phytochrome in the far-red absorbing form (P₇₃₀) were measured. The extent of mesocotyl inhibition observed 5 days later is proportional to the logarithm of P₇₃₀ concentration in mesocotyl tissue at the time of red light exposure.

The inhibition of mesocotyl growth by red light can be reversed partially by subsequent exposure to far-red light (730 mμ). Increasing doses of far-red light result in decreasing concentrations of P₇₃₀ as compared with the original P₇₃₀ level due to the preceding red light exposure. The reduced mesocotyl inhibition of seedings which had been exposed to red and far-red light is proportional to the logarithm of P₇₃₀ concentration remaining in the tissue at the end of the two light exposures.

This indicates that the same correlation exists between P₇₃₀ concentration and growth response whether the seedlings had been exposed to red light only or to red followed by far-red light.

     

Photocontrol of Hypocotyl Elongation in Light-Grown Cucumis sativus L. : Responses to Phytochrome Photostationary State and Fluence Rate

The effects of the calculated photostationary state of phytochrome (_c) and the photon fluence rate on the elongation growth of the hypocotyl of light-grown seedlings of Cucumis sativus L. are examined. Two threshold responses to _c are found at values of 0.06 and 0.43. At _c = 0.06, there is no response at any fluence rate. In the _c range 0.1 to 0.43, elongation growth does not respond to changes in _c. Above the second threshold (_c = 0.43), there is a strong response to changes in _c. At all values of _c at and above 0.1, there is a response to fluence rate. A linear relationship can be demonstrated between a factor comprised of the logarithm of phytochrome cycling rate (a fluence-rate-dependent process) and _c, and the growth response.     

Phytochrome B Is Not Detectable in the hy3 Mutant of Arabidopsis, Which Is Deficient in Responding to End-of-Day Far-Red Light Treatments

Immunoblot analysis using a monoclonal antibody specific tophytochrome B (phyB) suggest that this protein is undetectablein the hy3 mutant of Arabidopsis. Photophysiological experimentsrevealed that hy3 mutants do not display end-of-day far-redgrowth responses. Thus, this particular phytochrome responseseems to be mediated in large part by phyB. (Received September 20, 1991; Accepted September 26, 1991)     

Photoregulation of Phytochrome Synthesis in Germinating Embryos of Avena sativa L.

Hilton, J. R. and Thomas, B. 1987. Photoregulation of phytochromesynthesis in germinating embryos of Avena sativa L.—J.exp. Bot. 38: 1704–1712. The effect of light on the accumulation of phytochrome in germinatingAvena embryos was determined. A quantitative ELISA using monoclonalantibody AFRC MAC 56 was used to measure specifically type 1(or dark) phytochrome. A pulse of red light given after 14 himbibition but prior to the onset of type 1 phytochrome synthesis,strongly inhibited subsequent type 1 phytochrome accumulation.This effect of red light at 14 h was reversible by far-red lightindicating the involvement of phytochrome. Red light also inhibitedphytochrome synthesis after 18 h and 24 h imbibition but after24 h, far-red light did not reverse the effect. The effect ofred light treatment at 18 h was reversed by giving a pulse offar-red light at any time up to 30 h. Seed germination was notinfluenced by light under the conditions of these experiments.It is proposed that type 2 (or light) phytochrome may be responsiblefor photoregulation of type 1 phytochrome synthesis in germinatingAvena embryos. Key words: Photoregulation, phytochrome, seed.     

Physiological and Genetic Characterization of End-of-Day Far-Red Light Response in Maize Seedlings

Developmental responses associated with end-of-day far-red light (EOD-FR) signaling were investigated in maize (Zea mays subspecies mays) seedlings. A survey of genetically diverse inbreds of temperate and tropical/semitropical origins, together with teosinte (Zea mays subspecies parviglumis) and a modern hybrid, revealed distinct elongation responses. A mesocotyl elongation response to the EOD-FR treatment was largely absent in the tropical/semitropical lines, but both hybrid and temperate inbred responses were of the same magnitude as in teosinte, suggesting that EOD-FR-mediated mesocotyl responses were not lost during the domestication or breeding process. The genetic architecture underlying seedling responses to EOD-FR was investigated using the intermated B73 × Mo17 mapping population. Among the different quantitative trait loci identified, two were consistently detected for elongation and responsiveness under EOD-FR, but none were associated with known light signaling loci. The central role of phytochromes in mediating EOD-FR responses was shown using a phytochromeB1 phytochromeB2 (phyB1 phyB2) mutant series. Unlike the coleoptile and first leaf sheath, EOD-FR-mediated elongation of the mesocotyl appears predominantly controlled by gibberellin. EOD-FR also reduced abscisic acid (ABA) levels in the mesocotyl for both the wild type and phyB1 phyB2 double mutants, suggesting a FR-mediated but PHYB-independent control of ABA accumulation. EOD-FR elongation responses were attenuated in both the wild type and phyB1 phyB2 double mutants when a chilling stress was applied during the dark period, concomitant with an increase in ABA levels. We present a model for the EOD-FR response that integrates light and hormonal control of seedling elongation.Plants utilize a complex network of photoreceptors to monitor the spectral quality, fluence, direction, and duration of light (Smith, 1995). These photosensory pigments include phytochromes that sense red light (R; 580–690 nm) and far-red light (FR; 690–800 nm) and the cryptochromes, phototropins, and zeitlupes for blue light (380–495 nm) and UV-A light (320–380 nm). The light reflected and transmitted by the vegetation creates a canopy characterized by reductions in both the R-to-FR ratio (R:FR) and the photosynthetically active radiation (400–700 nm). This light environment induces adaptive biochemical and morphological responses known as the shade avoidance syndrome (Smith and Whitelam, 1997). These responses can be induced early in development, before canopy closure, through FR reflected from adjacent neighbor plants (Ballare et al., 1990) or from low-lying weeds (Rajcan and Swanton, 2001), which can negatively impact yields in maize (Zea mays subspecies mays; Rajcan et al., 2004), even if only present early in the growing season (Liu et al., 2009).R:FR signals are transduced by the phytochrome family of photoreceptors (Franklin and Whitelam, 2007b). In rice (Oryza sativa) and sorghum (Sorghum bicolor), three genes constitute the phytochrome family: PhytochromeA (PhyA), PhytochromeB (PhyB), and PhytochromeC (PhyC). In maize, an ancient alloploidization has doubled the family size to six: PhyA1, PhyA2, PhyB1, PhyB2, PhyC1, and PhyC2 (Sheehan et al., 2004). Although many similarities are apparent between maize and Arabidopsis (Arabidopsis thaliana) light response, there are significant differences between members of the phytochrome gene family in copy number and selection pressures that have resulted in the divergence of phytochrome signaling networks (Sawers et al., 2005; Sheehan et al., 2007). Thus far, only three phytochrome mutants have been characterized in maize: elongated mesocotyl1 (elm1), phyB1, and phyB2. The elm1 mutant carries a mutation in phytochromobilin synthase, necessary for the biosynthesis of the chromophore common to all phytochromes (Sawers et al., 2004). The mutation severely reduces the total phytochrome pool, but the weak nature of the allele enables a partial responsiveness to R and FR (Markelz et al., 2003). At maturity, elm1 mutants have elongated internodes, pale green leaves, and flower early (Sawers et al., 2002). Mutations at phyB1 and phyB2 also impair light signal transduction. At maturity, both PHYB1 and PHYB2 contribute to plant height, stem diameter, and sheath-internode length, but PHYB2 predominates in the control of flowering (Sheehan et al., 2007). Like the sorghum and rice phyB mutants (Childs et al., 1997; Takano et al., 2005; Kebrom et al., 2010), both elm1 and phyB1 phyB2 double mutants constitutively display several traits associated with low R:FR response (Sawers et al., 2002; Markelz et al., 2003; Sheehan et al., 2007).In Arabidopsis, R/FR-mediated responses are developmentally complex and involve the PIF proteins (Duek and Fankhauser, 2005) and many hormones including auxins (Tao et al., 2008), ethylene (Khanna et al., 2007), jasmonate (Moreno et al., 2009), and GA (Djakovic-Petrovic et al., 2007). In particular, there is a direct interaction between PIF and DELLA proteins that govern phytochrome-mediated elongation (de Lucas et al., 2008; Feng et al., 2008; Lorrain et al., 2008). DELLA proteins also regulate FR inhibition of germination by abscisic acid (ABA; Piskurewicz et al., 2009), suggesting an interaction between the PIFs and ABA signaling. Complex cross talk between light and temperature has also been reported (Franklin, 2009). In Arabidopsis, colder temperatures can repress the early-flowering phenotype of the phyB mutant (Halliday et al., 2003). These studies suggest a complex interplay between light, hormone, and temperature to fine-tune the elongation response.The end-of-day far-red light (EOD-FR) treatment consists of a pulse of FR given at subjective dusk (Kasperbauer, 1971) and triggers a circadian clock-gated response (Salter et al., 2003). EOD-FR treatments result in a minimal pool of active Pfr during the dark period (Fankhauser and Casal, 2004), and plants submitted to daily treatments display similar developmental responses to those elicited by a continuous photoperiod with low R:FR (Smith, 1994). One of the key features that contributed to the discovery of the phytochromes is the photoreversibility of the response (Borthwick et al., 1952). These low-fluence responses (LFRs) are induced or repressed by alternating R and FR treatments (Mancinelli, 1994). The LFR nature of EOD-FR in maize was previously demonstrated in 5-d-old mesocotyl and coleoptile tissues (Gorton and Briggs, 1980). The EOD-FR treatment offers several advantages over growing plants in continuous low R:FR, including exposing plants to relatively brief treatment periods, thus potentially reducing genotype × environment effects. It also facilitates kinetic assays of phytochrome response, as treatments are limited to a single point in the diurnal cycle and can be delivered at any stage in plant development. Finally, as relatively low fluences of light are needed to saturate EOD-FR responses, large populations of seedlings can be screened without the need for large numbers of FR light-emitting diodes (LEDs) or sophisticated light chambers.Here, we have examined EOD-FR-mediated responses in maize and its closest relative, teosinte (Zea mays subspecies parviglumis). A survey of genetically diverse maize and teosinte accessions revealed extensive tissue-specific variations in mesocotyl, coleoptile, and first leaf sheath elongation. EOD-FR responses were greatly attenuated in tropical/semitropical (TS) accessions but present in teosinte, temperate inbreds, and a modern commercial hybrid, suggesting that the EOD-FR response is plastic in Z. mays. To investigate the genetic regulation underlying seedling responses to EOD-FR, we performed a quantitative trait locus (QTL) analysis using the intermated B73 × Mo17 (IBM) recombinant inbred population. We identified several QTLs that regulate mesocotyl and first leaf sheath response to EOD-FR and show that these QTLs mediate tissue-specific responses. The phyB1 phyB2 mutant series was also evaluated, indicating that the two PhyB paralogs are largely redundant in mediating the EOD-FR response. Pharmacological assays revealed a major role for GA in promoting mesocotyl, but not coleoptile or first leaf sheath, elongation in response to EOD-FR treatments. In contrast, EOD-FR reduced mesocotyl ABA levels. A chill treatment (10°C) applied during dark breaks attenuated EOD-FR elongation responses. Based on these observations, we discuss a model that integrates temperature, light, and hormonal inputs in the regulation of mesocotyl elongation.     

Dichroic Orientation of Phytochrome Intermediates in the Pathway from PR to PFR as Analyzed by Double Laser Flash Irradiations in Polarotropism of Adiantum Protonemata

The polarotropic response in protonemata of the fern Adiantumis regulated by phytochrome (Kadota et al. 1984); P_R and P_FRhave been shown to be dichroically oriented parallel and normalto the cell surface, respectively (Kadota et al. 1982). Thischange in the dichroic orientation of phytochrome during photoconversionwas analyzed by a newly-built, polarization plane-rotatabledouble laser flash irradiator. A polarotropic response was effectivelyinduced with a flash of polarized red (640 nm) light (6xl0^–7s) having the vibration plane of the electrical vector parallelto the protonemal cell axis. When a flash of polarized far-red(710 nm) light (6xl0^–7s) was given 30 sec after the redflash, the red flash-induced response was reversed by a far-redflash vibrating normal to the cell axis but not by one vibratingparallel. However, when given 2 µs or 2 ms after the redflash, the polarotropic response was not reversed by a polarizedfar-red flash vibrating normal to the cell axis but was reversedby a parallel-vibrating flash. These results suggest that theorientation of phototransformation intermediates existing 2µs or 2 ms after a red flash is still parallel to thecell surface, and that the change in the orientation of phytochromemolecules occurs between 2 ms and 30 s after the red flash. (Received February 3, 1986; Accepted April 23, 1986)     

A Comparison of Seed and Seedling Phytochrome in Avena sativa L. using Monoclonal Antibodies

Hilton, J.R. and Thomas, B. 1985. A comparison of seed and seedlingphytochrome in Avena saliva L.using monoclonal antibodies.—J.exp. Bot. 36: 1937–1946.The kinetics of phytochrome accumulationduring imbibition and germination of seeds of Avena saliva L.cv. Saladin has been determined in vivo by spectrophotometryand in extracts by using Enzyme–Linked Immunosorbent Assay(EL1SA). In vivo measurements show two phases of phytochromeincrease. The first occurs during the initial 2 h of imbibitionand is associated with the hydration of the seed proteins; thesecond larger increase begins after 16 h, due probably to denovo synthesis. An ELISA using monoclonal antibodies purifiedfrom dark grown Avena seedlings detected only the second increasein phytochrome content. Mixing experiments indicate that theinability to detect phytochrome by ELISA during the first 16h is not due to the presence of inhibitors in the extracts.It is concluded that pre–existent seed phytochrome isantigenically dissimilar to seedling phytochrome. These twopools of phytochrome are stable and unstable respectively withregard to Pfr destruction. Key words: Immunology, phytochrome, seed     

Response of excised Avena coleoptile segments to red and far-red light

Summary In seeking a simple, red light-promoted straight growth test in which phytochrome assays may be conducted without interference by protochlorophyll, the response of excised Avena coleoptile segments to red and far-red light was re-examined. The elongation of apical (non-decapitated) segments is promoted by a brief exposure to red light, and this effect is almost completely nullified by an immediately subsequent exposure to far-red light. Although growth promotion by red light occurs in distilled water alone, the effect is greater on a medium consisting of 0.02 M phosphate buffer, pH 6.2 to 6.4, with 1 to 2% sucrose. Over the pH range 4.5 to 7.4, dark-growth decreases with increasing pH, but the absolute increment brought about by red light is nearly constant. Elongation appears to be entirely the result of increased cell size.Contrary to previous reports, similar results can be obtained with subapical (decapitated) coleoptile segments, although the absolute magnitude of the response is reduced.Research carried out at Brookhaven National Laboratory under the auspices of the U.S. Atomic Energy Commision.     

Phytochrome Regulation of the Response to Exogenous Gibberellins by Epicotyls of Vigna sinensis

The elongation rate of cowpea epicotyls from whole cowpea (Vigna sinensis) seedlings and derooted and debladed plants (explants) increased after the main light period (8-hour duration) was extended with either continuous low intensity tungsten light or brief (5 minutes) far-red (FR) irradiation. This end-of-day FR effect was reversed by red (R) irradiation suggesting the involvement of phytochrome. These results confirm and extend those obtained previously with other species. Localization studies indicate the epicotyl to be the site of the photoreceptor. Treatment of cowpea seedlings with paclobutrazol, a gibberellin (GA) biosynthetic inhibitor, abolished the FR promoted epicotyl elongation, indicating a role for GAs in this process. There was no significant difference in epicotyl elongation rates of R plus FR irradiated explants treated with GA₁ or GA₂₀ and R irradiated explants treated with GA₁. However, R irradiation inhibited subsequent epicotyl elongation of GA₂₀ treated explants. Moreover, the observation, using GC-MS, that GA₁ and GA₂₀ are native GAs in cowpea lends support to the concept that phytochrome may control the conversion of endogenous GA₂₀ to GA₁ in cowpea.     

Response of Chlamydomonas to Temperature Change

SYNOPSIS. Response of Chlamydomonas to temperature change was investigated. When the temperature of the medium was suddenly increased (decreased) the abrupt velocity rise (drop) was observed. This abrupt velocity change was induced immediately after the temperature change. Then, the high (low) level of the velocity was maintained for a few minutes. Finally the velocity decreased (increased), tending to a stationary level at the new temperature with the decay time of a few minutes. The rate of the temperature change determined the magnitude of response. The threshold value was found in the rate of the temperature change to produce the transient change of the velocity. It was ∼ 0.2 C/sec.     

Phytochrome chromophore biosynthesis. Treatment of tetrapyrrole-deficient Avena explants with natural and non-natural bilatrienes leads to formation of spectrally active holoproteins

Etiolated Avena seedlings grown in the presence of 4-amino-5-hexynoic acid, an inhibitor of 5-aminolevulinic acid synthesis in plants, contain less than 10% of the spectrally detectable levels of phytochrome found in untreated seedlings (Elich, T.D., and Lagarias, J.C. (1988) Plant Physiol. 88, 747-751). In this study, incubation of explants from such seedlings with [14C]biliverdin IX alpha led to rapid covalent incorporation of radiolabel into a single 124-kDa polypeptide in soluble protein extracts. Immunoprecipitation experiments confirmed that this protein was phytochrome. Parallel experiments were performed with four unlabeled linear tetrapyrroles, the naturally occurring biliverdin IX alpha isomer, two non-natural isomers, biliverdin XIII alpha and biliverdin III alpha, and phycocyanobilin-the cleaved prosthetic group of the light-harvesting antenna protein C-phycocyanin. In all cases, except for the III alpha isomer of biliverdin, a time-dependent recovery of photoreversible phytochrome was observed. The newly formed phytochrome obtained after incubation with biliverdin IX alpha exhibited spectral characteristics identical with those of the native protein. In contrast, the spectral properties of phytochromes formed during incubation with biliverdin XIII alpha and phycocyanobilin differed significantly from those of the native chromoprotein. These results indicate that biliverdin IX alpha is an intermediate in the biosynthesis of the phytochrome chromophore and that phytochromes with prosthetic groups derived from bilatrienes having non-natural D-ring substituents are photochromic.