scholarly journals BBX16 mediates the repression of seedling photomorphogenesis downstream of the GUN1-GLK1 module during retrograde signaling

2021 ◽  
Author(s):  
Nil Veciana ◽  
Guiomar Martin ◽  
Pablo Leivar ◽  
Elena Monte
Keyword(s):  
Transcription Factor ◽  
Seedling Development ◽  
Transcriptional Network ◽  
High Light ◽  
Nuclear Genes ◽  
Retrograde Signaling ◽  
Light Conditions ◽  
Bifurcation Mechanism ◽  
Branching Point ◽  
Direct Target

Plastid-to-nucleus retrograde signals (RS) initiated by dysfunctional chloroplasts impact photomorphogenic development. We previously showed that the transcription factor GLK1 acts downstream of the RS-regulator GUN1 in photodamaging conditions to regulate not only the well-established expression of photosynthesis-associated nuclear genes (PhANGs) but also to regulate seedling morphogenesis. Specifically, the GUN1/GLK1 module inhibits the light-induced PIF-repressed transcriptional network to suppress cotyledon development when chloroplast integrity is compromised, modulating the area exposed to potentially damaging high light. However, how the GUN1/GLK1 module inhibits photomorphogenesis upon chloroplast damage remained undefined. Here, we report the identification of BBX16 as a novel direct target of GLK1. BBX16 is induced and promotes photomorphogenesis in moderate light and it is repressed via GUN1/GLK1 after chloroplast damage. Additionally, we show that BBX16 represents a regulatory branching point downstream of GUN1/GLK1 in the regulation of PhANG expression and seedling development upon RS activation. The gun1 phenotype in lincomycin and the gun1-like phenotype of GLK1OX are markedly suppressed in gun1bbx16 and GLK1OXbbx16. This study identifies BBX16 as the first member of the BBX family involved in RS, and defines a molecular bifurcation mechanism operated by GLK1/BBX16 to optimize seedling deetiolation, and to ensure photoprotection in unfavorable light conditions.

Control of light-dependent keto carotenoid biosynthesis in Nostoc 7120 by the transcription factor NtcA

2016 ◽  
Vol 71 (9-10) ◽  
pp. 303-311 ◽  
Author(s):  
Gerhard Sandmann ◽  
Jürgen Mautz ◽  
Jürgen Breitenbach
Keyword(s):  
Transcription Factor ◽  
Redox State ◽  
Photosynthetic Electron Transport ◽  
Carotenoid Biosynthesis ◽  
High Light ◽  
Light Conditions ◽  
Promoter Regions ◽  
Carotenogenic Genes ◽  
Pcc 7120 ◽  
Β Carotene

Abstract In Nostoc PCC 7120, two different ketolases, CrtW and CrtO are involved in the formation of keto carotenoids from β-carotene. In contrast to other cyanobacteria, CrtW catalyzes the formation of monoketo echinenone whereas CrtO is the only enzyme for the synthesis of diketo canthaxanthin. This is the major photo protective carotenoid in this cyanobacterium. Under high-light conditions, basic canthaxanthin formation was transcriptionally up-regulated. Upon transfer to high light, the transcript levels of all investigated carotenogenic genes including those coding for phytoene synthase, phytoene desaturase and both ketolases were increased. These transcription changes proceeded via binding of the transcription factor NtcA to the promoter regions of the carotenogenic genes. The binding was absolutely dependent on the presence of reductants and oxo-glutarate. Light-stimulated transcript formation was inhibited by DCMU. Therefore, photosynthetic electron transport is proposed as the sensor for high-light and a changing redox state as a signal for NtcA binding.

Light Absorption and Partitioning in Response to Nitrogen in Apple Leaves

HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 541a-541
Author(s):  
Lailiang Cheng ◽  
Leslie H. Fuchigami ◽  
Patrick J. Breen
Keyword(s):  
High Light ◽  
Thermal Dissipation ◽  
Photochemical Quenching ◽  
Light Conditions ◽  
Psii Efficiency ◽  
Fluorescence Measurements ◽  
Free Radical Formation ◽  
Highly Correlated ◽  
Non Photochemical Quenching ◽  
Leaf N

Bench-grafted Fuji/M26 apple trees were fertigated with different concentrations of nitrogen by using a modified Hoagland solution for 6 weeks, resulting in a range of leaf N from 1.0 to 4.3 g·m–2. Over this range, leaf absorptance increased curvilinearly from 75% to 92.5%. Under high light conditions (1500 (mol·m–2·s–1), the amount of absorbed light in excess of that required to saturate CO2 assimilation decreased with increasing leaf N. Chlorophyll fluorescence measurements revealed that the maximum photosystem II (PSII) efficiency of dark-adapted leaves was relatively constant over the leaf N range except for a slight drop at the lower end. As leaf N increased, non-photochemical quenching under high light declined and there was a corresponding increase in the efficiency with which the absorbed photons were delivered to open PSII centers. Photochemical quenching coefficient decreased significantly at the lower end of the leaf N range. Actual PSII efficiency increased curvilinearly with increasing leaf N, and was highly correlated with light-saturated CO2 assimilation. The fraction of absorbed light potentially used for free radical formation was estimated to be about 10% regardless of the leaf N status. It was concluded that increased thermal dissipation protected leaves from photo-oxidation as leaf N declined.

Changes in the Stoichiometry of Photosystem II Components as an Adaptive Response to High-Light and Low-Light Conditions during Growth

1986 ◽  
Vol 41 (5-6) ◽  
pp. 597-603 ◽  
Author(s):  
Aloysius Wild ◽  
Matthias Höpfner ◽  
Wolfgang Rühle ◽  
Michael Richter
Keyword(s):  
Photosystem Ii ◽  
Functional Organization ◽  
Photosynthetic Apparatus ◽  
High Light ◽  
Molar Ratio ◽  
Light Conditions ◽  
Low Light ◽  
Pigment System ◽  
Transport Chain ◽  
The One

The effect of different growth light intensities (60 W·m-2, 6 W·m-2) on the performance of the photosynthetic apparatus of mustard plants (Sinapis alba L.) was studied. A distinct decrease in photosystem II content per chlorophyll under low-light conditions compared to high-light conditions was found. For P-680 as well as for Oᴀ and Oв protein the molar ratio between high-light and low-light plants was 1.4 whereas the respective concentrations per chlorophyll showed some variations for P-680 and Oᴀ on the one and Oв protein on the other hand.In addition to the study of photosystem II components, the concentrations of PQ, Cyt f, and P-700 were measured. The light regime during growth had no effect on the amount of P-700 per chlorophyll but there were large differences with respect to PQ and Cyt f. The molar ratio for Cyt f and PQ between high- and low-light leaves was 2.2 and 1.9, respectively.Two models are proposed, showing the functional organization of the pigment system and the electron transport chain in thylakoids of high-light and low-light leaves of mustard plants.

scholarly journals Effects of alkalinity and salinity at low and high light intensity on hydrogen isotope fractionation of long-chain alkenones produced by <i>Emiliania huxleyi</i>

2017 ◽  
Vol 14 (24) ◽  
pp. 5693-5704 ◽  
Author(s):  
Gabriella M. Weiss ◽  
Eva Y. Pfannerstill ◽  
Stefan Schouten ◽  
Jaap S. Sinninghe Damsté ◽  
Marcel T. J. van der Meer
Keyword(s):  
Light Intensity ◽  
Environmental Conditions ◽  
Hydrogen Isotope ◽  
Isotope Fractionation ◽  
Emiliania Huxleyi ◽  
High Light Intensity ◽  
High Light ◽  
Light Conditions ◽  
Low Light ◽  
Long Chain

Abstract. Over the last decade, hydrogen isotopes of long-chain alkenones have been shown to be a promising proxy for reconstructing paleo sea surface salinity due to a strong hydrogen isotope fractionation response to salinity across different environmental conditions. However, to date, the decoupling of the effects of alkalinity and salinity, parameters that co-vary in the surface ocean, on hydrogen isotope fractionation of alkenones has not been assessed. Furthermore, as the alkenone-producing haptophyte, Emiliania huxleyi, is known to grow in large blooms under high light intensities, the effect of salinity on hydrogen isotope fractionation under these high irradiances is important to constrain before using δDC37 to reconstruct paleosalinity. Batch cultures of the marine haptophyte E. huxleyi strain CCMP 1516 were grown to investigate the hydrogen isotope fractionation response to salinity at high light intensity and independently assess the effects of salinity and alkalinity under low-light conditions. Our results suggest that alkalinity does not significantly influence hydrogen isotope fractionation of alkenones, but salinity does have a strong effect. Additionally, no significant difference was observed between the fractionation responses to salinity recorded in alkenones grown under both high- and low-light conditions. Comparison with previous studies suggests that the fractionation response to salinity in culture is similar under different environmental conditions, strengthening the use of hydrogen isotope fractionation as a paleosalinity proxy.

scholarly journals Occurrence of neoxanthin and lutein epoxide cycle in parasitic Cuscuta species.

2008 ◽  
Vol 55 (1) ◽  
pp. 183-190 ◽  
Author(s):  
Jerzy Kruk ◽  
Renata Szymańska
Keyword(s):  
Substrate Specificity ◽  
Xanthophyll Cycle ◽  
Higher Plants ◽  
Light Stress ◽  
High Light ◽  
Light Conditions ◽  
Strong Light ◽  
Zeaxanthin Epoxidase ◽  
Typical Response ◽  
Cuscuta Species

In the present study, xanthophyll composition of eight parasitic Cuscuta species under different light conditions was investigated. Neoxanthin was not detected in four of the eight species examined, while in others it occurred at the level of several percent of total xanthophylls. In C. gronovii and C. lupuliformis it was additionally found that the neoxanthin content was considerably stimulated by strong light. In dark-adapted plants, lutein epoxide level amounted to 10-22% of total xanthophylls in only three species, the highest being for C. lupuliformis, while in others it was below 3%, indicating that the lutein epoxide cycle is limited to only certain Cuscuta species. The obtained data also indicate that the presence of the lutein epoxide cycle and of neoxanthin is independent and variable among the Cuscuta species. The xanthophyll cycle carotenoids violaxanthin, antheraxanthin and zeaxanthin were identified in all the examined species and occurred at the level found in other higher plants. The xanthophyll and lutein epoxide cycle pigments showed typical response to high light stress. The obtained results also suggest that the ability of higher plants to synthesize lutein epoxide probably does not depend on the substrate specificity of zeaxanthin epoxidase but on the availability of lutein for the enzyme.

Stomatal aperture can compensate altered stomatal density in Arabidopsis thaliana at growth light conditions

2006 ◽  
Vol 33 (11) ◽  
pp. 1037 ◽  
Author(s):  
Dirk Büssis ◽  
Uritza von Groll ◽  
Joachim Fisahn ◽  
Thomas Altmann
Keyword(s):  
Arabidopsis Thaliana ◽  
Stomatal Conductance ◽  
Stomatal Density ◽  
Co2 Assimilation ◽  
High Light ◽  
Stomatal Aperture ◽  
Photochemical Quenching ◽  
Light Conditions ◽  
Wild Type ◽  
Light Intensities

Stomatal density of transgenic Arabidopsis thaliana plants over-expressing the SDD1 (stomatal density and distribution) gene was reduced to 40% and in the sdd1-1 mutant increased to 300% of the wild type. CO2 assimilation rate and stomatal conductance of over-expressers and the sdd1-1 mutant were unchanged compared with wild types when measured under the light conditions the plants were exposed to during growth. Lower stomatal density was compensated for by increased stomatal aperture and conversely, increased stomatal density was compensated for by reduced stomatal aperture. At high light intensities the assimilation rates and stomatal conductance of SDD1 over-expressers were reduced to 80% of those in wild type plants. Areas beneath stomata and patches lacking stomata were analysed separately. In areas without stomata, maximum fluorescence yield (Fv / Fm) and quantum yield of photosystem II (Φ PSII) were significantly lower than in areas beneath stomata. In areas beneath stomata, Fv / Fm and Φ PSII were identical to levels measured in wild type leaves. At high light intensities over-expressers showed decreased photochemical quenching (qP) compared with wild types. However, the decrease of qP was significantly stronger in areas without stomata than in mesophyll areas beneath stomata. At high CO2 partial pressures and high light intensities CO2 assimilation rates of SDD1 over-expressers did not reach wild type levels. These results indicate that photosynthesis in SDD1 over-expressers was reduced because of limiting CO2 in areas furthest from stomata at high light.

The Fate of Nitrofen in Rape, Redroot Pigweed, and Green Foxtail

Weed Science ◽  
1971 ◽  
Vol 19 (5) ◽  
pp. 555-558 ◽  
Author(s):  
D. Hawton ◽  
E. H. Stobbe
Keyword(s):  
Light Intensity ◽  
Brassica Campestris ◽  
Molecular Size ◽  
Amaranthus Retroflexus ◽  
High Light ◽  
Setaria Viridis ◽  
Light Conditions ◽  
Ether Linkage ◽  
Redroot Pigweed ◽  
Green Foxtail

The fate of 2,4-dichlorophenyl p-nitrophenyl ether (nitrofen) in the foliage of rape (Brassica campestris L. ‘Echo’), redroot pigweed (Amaranthus retroflexus L.), and green foxtail (Setaria viridis (L.) Beauv.) was investigated with the aid of 14C-nitrofen. Only limited amounts of the label were translocated in these species. Plants treated with 14C-nitrofen under high light conditions produced several labelled compounds of different molecular size and chromatographic properties. The time at which these compounds were first detectable depended on light intensity. At least two of these compounds are lipid-nitrofen conjugates or nitrofen polymers and others may be formed by cleavage of nitrofen at the ether linkage.

scholarly journals The Response Regulator RpaB Binds to the Upstream Element of Photosystem I Genes To Work for Positive Regulation under Low-Light Conditions in Synechocystis sp. Strain PCC 6803

2008 ◽  
Vol 191 (5) ◽  
pp. 1581-1586 ◽  
Author(s):  
Yurie Seino ◽  
Tomoko Takahashi ◽  
Yukako Hihara
Keyword(s):  
Photosystem I ◽  
Promoter Activity ◽  
Response Regulator ◽  
Core Promoter ◽  
High Light ◽  
Light Conditions ◽  
Low Light ◽  
Positive Regulation ◽  
Upstream Element ◽  
Pcc 6803

ABSTRACT The coordinated high-light response of genes encoding subunits of photosystem I (PSI) is achieved by the AT-rich region located just upstream of the core promoter in Synechocystis sp. strain PCC 6803. The upstream element enhances the basal promoter activity under low-light conditions, whereas this positive regulation is lost immediately after the shift to high-light conditions. In this study, we focused on a high-light regulatory 1 (HLR1) sequence included in the upstream element of every PSI gene examined. A gel mobility shift assay revealed that a response regulator RpaB binds to the HLR1 sequence in PSI promoters. Base substitution in the HLR1 sequence or decrease in copy number of the rpaB gene resulted in decrease in the promoter activity of PSI genes under low-light conditions. These observations suggest that RpaB acts as a transcriptional activator for PSI genes. It is likely that RpaB binds to the HLR1 sequence under low-light conditions and works for positive regulation of PSI genes and for negative regulation of high-light-inducible genes depending on the location of the HLR1 sequence within target promoters.

Interactions entre mitochondries et chloroplastes dans la cellule. II. Action du DBMIB, de l'antimycine A et du FCCP sur la spore de Funaria hygrometrica

1977 ◽  
Vol 55 (12) ◽  
pp. 1650-1659 ◽  
Author(s):  
D. Chevallier ◽  
R. Douce ◽  
F. Nurit
Keyword(s):  
Cytochrome Oxidase ◽  
Dark Respiration ◽  
High Light ◽  
Light Conditions ◽  
Oxygen Production ◽  
Low Light ◽  
Funaria Hygrometrica ◽  
Light Intensities

The effect of DBMIB, antimycine A, and FCCP on respiration and photosynthesis of intact chlorophyllic moss (Funaria hygrometrica) spore was investigated.Antimycine A (1 μM) strongly inhibited dark respiration, was without effect on photosynthesis at high light intensities (above the saturation plateau values), and stimulated photosynthesis at low light intensities (below the saturation plateau values).DBMIB (3 μM) inhibited photosynthesis and was without effect, even under light conditions, on the dark respiration. Low amount of FCCP (3 μM) partially inhibited oxygen production at high light intensities. In this case, the inhibition observed was partially relieved by 1 μM antimycine A or 30 μM of KCN; higher concentration of FCCP totally inhibited the oxygen production.It seems likely, therefore, that in the chlorophyllic moss spore the cytochrome oxidase pathway is not functioning under high light intensities and that this inhibition of respiration is attributable to the low cytoplasmic ADP:ATP ratio.

Sign in / Sign up

Export Citation Format

Share Document