WHIRLY1-deficient chloroplasts display enhanced formation of cyclobutane pyrimidine dimers during exposure to UV-B radiation.

The single-stranded DNA/RNA binding protein WHIRLY1 is a major chloroplast nucleoid-associated protein required for the compactness of nucleoids. Most nucleoids in chloroplasts of WHIRLY1-knockdown barley plants are less compact compared to nucleoids in wild-type plants. The reduced compaction leads to an enhanced optical cross-section, which may cause the plastid DNA to be a better target for damaging UV-B radiation. To investigate this hypothesis, primary foliage leaves, chloroplasts, and nuclei from wild-type and WHIRLY1-knockdown plants were exposed to experimental UV-B radiation. Thereafter, total, genomic and plastid DNA were isolated, respectively, and analyzed for the occurrence of cyclobutane pyrimidine dimers (CPDs), which is a parameter for genome stability. The results of this study revealed that WHIRLY1-deficient chloroplasts had strongly enhanced DNA damages, whereas isolated nuclei from the same plant line were not more sensitive than nuclei from the wild-type, indicating that WHIRLY1 has different functions in chloroplasts and nucleus. This supports the hypothesis that the compaction of nucleoids may provide protection against UV-B radiation.

Downsizing in plants-UV light induces pronounced morphological changes in the absence of stress.

Ultraviolet (UV) light induces a stocky phenotype in many plant species. In this study, we investigate this effect with regard to specific UV wavebands (UV-A or UV-B) and the cause for this dwarfing. UV-A- or UV-B-enrichment of growth light both resulted in a smaller cucumber (Cucumis sativus L.) phenotype, exhibiting decreased stem and petiole lengths and leaf area (LA). Effects were larger in plants grown in UV-B- than in UV-A-enriched light. In plants grown in UV-A-enriched light, decreases in stem and petiole lengths were similar independent of tissue age. In the presence of UV-B radiation, stems and petioles were progressively shorter the younger the tissue. Also, plants grown under UV-A-enriched light significantly reallocated photosynthates from shoot to root and also had thicker leaves with decreased specific LA. Our data therefore imply different morphological plant regulatory mechanisms under UV-A and UV-B radiation. There was no evidence of stress in the UV-exposed plants, neither in photosynthetic parameters, total chlorophyll content, or in accumulation of damaged DNA (cyclobutane pyrimidine dimers). The abscisic acid content of the plants also was consistent with non-stress conditions. Parameters such as total leaf antioxidant activity, leaf adaxial epidermal flavonol content and foliar total UV-absorbing pigment levels revealed successful UV acclimation of the plants. Thus, the UV-induced dwarfing, which displayed different phenotypes depending on UV wavelengths, occurred in healthy cucumber plants, implying a regulatory adjustment as part of the UV acclimation processes involving UV-A and/or UV-B photoreceptors.

Solar UV-B effects on composition and UV screening efficiency of foliar phenolics in Arabidopsis thaliana are augmented by temperature.

The accumulation of foliar phenolics constitutes one strategy of plants against the potentially harmful effects of ultraviolet-B and A (UV-B, UV-A) radiation. These compounds protect photosensitive tissues by shielding and antioxidative function. It is unknown, however, whether seasonal acclimation to natural conditions may modify the UV-B effect on phenylpropanoid composition and localisation, and thus their screening efficiency. To address this debate, a field experiment with the wildtype of Arabidopsis thaliana accession Landsberg erecta (Ler) was implemented over a whole year with plants exposed to different UV-filter treatments. While seasonal increases of UV-B radiation had a slight negative effect on the amount of hydroxycinnamic acids (HCAs), low temperatures increased foliar HCAs. HCAs, however, did not contribute substantially to seasonal changes of in vivo UV absorbance. Kaempferol and quercetin derivatives increased significantly under ambient UV-B radiation, and low temperature interacted with this effect. A shift of epidermal UV-A shielding from kaempferol to quercetin derivatives was elucidated in UV-B presence. Despite this, a substantial 20-fold increase of quercetin derivatives, during periods with high irradiance and low temperature, did not affect UV absorbance leading to the conclusion that quercetin accumulation was not exclusively in epidermal vacuoles. Using confocal microscopy, the potential occurrence of quercetin in mesophyll cells was demonstrated in plants grown with experimental UV-B radiation at low temperature for the first time in A. thaliana. The presented study discusses the idea that cross-talk of UV-B radiation and temperature might adjust the physiological function of quercetin from an (epidermal) screening to an antioxidant substance.

UV-A screening in Cladophora sp. lowers internal UV-A availability and photoreactivation as compared to non-UV screening in Ulva intestinalis.

In the Baltic Sea, two co-occurring green macroalgae Cladophora sp. and Ulva intestinalis grow in the upper eulittoral. Due to regular and high sunlight exposure in their habitat, both species need resistance mechanisms to protect themselves against ultraviolet-B (UV-B)-induced DNA damage. While Cladophora sp. possesses efficient screening of UV-B and ultraviolet-A (UV-A) radiation, U. intestinalis was recently shown to have higher DNA repair by UVA-driven photoreactivation than Cladophora sp. [F. Pescheck and W. Bilger, Mar. Biol., 2018, 165, 132]. In the present study, the hypothesis that the screening of UV-A radiation limits internal UV-A availability for photoreactivation in Cladophora sp. was tested. Both species had identical and much lower fractions of damaged DNA when sampled in situ under direct sunlight as expected based on a photophysical prediction. To quantify the effect of UV-A screening spectrally and physiologically, in vivo UV screening spectra were determined and the UV-A photon flux dependency of photoreactivation was investigated for both species. Identical intrinsic photoreactivation rates were revealed by the applied correction for internal UV-A photon flux density and under irradiation with visible radiation which is not screened by the UV absorbing compounds in Cladophora sp. Natural sunlight was weighted with in vivo action spectra for DNA damage induction and light-dependent repair. The resulting spectrum was further corrected for the apparent UV screening spectra of both species to calculate the species-specific internal ratios of DNA damaging and photoreactivating photons. This photophysical modelling improves the understanding of UV damage and tolerance mechanisms in the two co-occurring green macroalgae under solar irradiation.

High impact of seasonal temperature changes on acclimation of photoprotection and radiation-induced damage in field grown Arabidopsis thaliana.

At temperate latitudes environmental factors such as irradiance, including ultraviolet-B radiation (UV-B, 280-315 nm), temperature and day length vary widely over the course of a year in a concerted way. In the present study physiological acclimation of photoprotection, growth and development of the model organism Arabidopsis thaliana were correlated to these strongly but gradually changing conditions in a one year field study. Plants were sown in the field avoiding any manipulation (and abrupt change) during their life. Developmental rate was strongly dependent on prevailing temperature. Moderate signs of light stress in form of photoinhibition at photosystem II were significantly related to solar irradiances while amount of DNA damage was low and not correlated to UV-B irradiance. Although all the markers were hypothesized to primarily react to radiation, multiple regression analysis showed at least a similarly strong influence of temperature as that of light. Especially for the classical UV screening compounds a positive correlation to UV-B radiation during the course of the year was absent, whereas there was a significant negative correlation between temperature and quercetin content. The sum of violaxanthin cycle pigments was correlated to both, irradiance and temperature, but with opposite sign. Epidermal UV-B transmittance was also much better related to air temperature than to UV-B irradiance. The data show that under natural conditions temperature has at least a similar importance for photoprotective acclimation and partially also for photosensitivity as solar irradiance.

UVB-induced DNA and photosystem II damage in two intertidal green macroalgae: distinct survival strategies in UV-screening and non-screening Chlorophyta.

Ultraviolet-B-induced (UVB, 280-315 nm) accumulation of cyclobutane pyrimidine dimers (CPDs) and deactivation of photosystem II (PS II) was quantified in two intertidal green macroalgae, Ulva clathrata and Rhizoclonium riparium. The species were chosen due to their shared habitats but contrasting UVB screening potentials. In the non-screening U. clathrata CPDs accumulated and PS II activity declined as a linear function of applied UVB irradiance. In R. riparium UVB-induced damage was significantly lower than in U. clathrata, demonstrating an efficient UVB protection of DNA and PS II by screening. Based on the UVB irradiance reaching the chloroplasts, both species showed an identical intrinsic sensitivity of PS II towards UVB, but DNA lesions accumulated slower in U. clathrata. While repair of CPDs was similar in both species, U. clathrata was capable of restoring its PS II function decidedly faster than R. riparium. In R. riparium efficient screening may represent an adaptation to its high light habitat, whereas in U. clathrata high repair rates of PS II appear to be important to survive natural UVB exposure. The role of shading of the nucleus by the large chloroplasts in U. clathrata is discussed.