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At least 19 recordsLinked to original sources

Lightness induction in the S-cone pathway.

Lightness induction is classically regarded as a contrast phenomenon limited to pathways which process luminance information. To determine if lightness induction can also occur in the chromatic domain, this phenomenon was studied with stimuli visible only to the short wavelength sensitive (S)-cones which have post-receptoral connections limited to chromatic pathways. The lightness of an object visible only to S-cones was found to be dependent on the relative intensity of its background in a manner similar to achromatic, luminance stimuli. Less intense (dark) backgrounds made the object appear lighter, while more intense (light) backgrounds made the same object appear darker. These results indicate a commonality among lightness induction effect in the processing of chromatic and luminance information.

Adaptation, Ocular

[Nicotinamide coenzymes at the early stages of light induction of carotenogenesis in the Neurospora crassa mycelium].

Changes in the concentration of NAD+, NADH, NADP+ and NADPH in the mycelium of the NADase free mutant of Neurospora crassa were studied during the latent stage of light induction of carotenogenesis. A 30 minute illumination by visible light brought about a stable decrease in the NADH/NAD+NADH ratio, exerting no effect on the NADPH/NADP+NADPH ratio. At the same time the NADP+/NAD+ ratio increased. These changes occurred only when illumination induced carotenoid accumulation in the N. crassa mycelium.

Carotenoids

Counterphase lightness induction.

When half-cycle wide mid-grey test elements are superimposed on a black and white square wave induction grating, their apparent lightness is a linear function of their phase relationship with the induction grating; being judged lightest when in phase with the black bars of the grating, and darkest when in phase with the white bars. This finding justifies the use of the term "counterphase induction" to describe the effect, and emphasizes the similarity between this effect and McCourt's (1982) [Vision Res. 22, 119-134] grating induction effect. The fact that the same linear function holds whether the test elements are square or rectangular favours a global over a local explanation.

Female

Light induction of the Euglena chloroplast protein synthesis elongation factors: relative effectiveness of different wavelength ranges.

The abilities of different wavelength ranges of light to promote the increase in the activities of the Euglena chloroplast protein synthesis elongation factors (EFs) during chloroplast biogenesis have been determined. Blue light was far more effective than either green light or red light in increasing the level of chloroplast EF-G, a nuclear encoded gene product. This observation suggests that the induction of EF-Gchl is under the control of the blue photoreceptor that has been identified in Euglena. Blue light was also the most effective wavelength range in facilitating the increase in EF-Ts, a nuclear gene product, and EF-Tu, a chloroplast gene product. However, red light and surprisingly green light were also effective. These results are not consistent with either of the known blue or blue/red photoreceptor systems in Euglena being the sole component involved in the light induction of these two factors and suggest that a green photoresponse may also be important in the development of the chloroplast. The specific activity of the Euglena mitochondrial protein biosynthetic translocase (EF-Gmt) decreased in cells exposed to light. Blue light caused an immediate decline in EF-Gmt activity; whereas, there was a temporal delay in the decrease in EF-Gmt activity when cells were exposed to either red or green light.

Chloroplasts

Black light induction of skin tumors in mice.

Albino inbred mice (A/J strain exposed to 40-w black light fluorescent lamps (BLB) for 12 hr a day for up to a year developed inflammatory and hyperplastic responses on hairless ear and tail skin, but not on back skin covered by hair. After 1 year of such exposure, many individuals developed papillomas, carcinomas, and sarcomas on their ears and tails. It may be concluded that black light is a skin carcinogen for A/J mice.

Animals

Photosensitized UVA light induction of the SOS response in Escherichia coli.

Several of the factors controlling the extent of the ultraviolet light (and particularly of UVA 320 nm less than lambda less than 380 nm) induced SOS response in E. coli have been studied using a sfiA::lacZ fusion. The decreased 254 nm induced sfiA expression level triggered by a UVA-induced growth delay (Caldeira de Araujo A. & Favre A. (1986) Embo J., 5, 175-179), is closely mimicked by a transient chloramphenicol protein synthesis inhibition. In a nuvA mutant strain (lacking the growth delay effect), UVA light triggers a 30-40% lower SOS response at temperatures higher than 20 degrees C when illumination is performed under anaerobic conditions: endogenous oxygen-mediated photosensitized reactions appear to contribute to the SOS response. In contrast to the temperature independence of the sfiA induction levels obtained after 254 nm irradiation, the UVA induced response is 30-60% lower when the temperature (T) increases from a value lower than 10 degrees C to a value higher than 20 degrees C. This indicates that detoxifying enzymes play a role at T greater than 20 degrees C. Also the in vitro photooxydation of NADH to give NAD+ is described and its possible role in endogenous photosensibilizations discussed. To explain the contrasted mutagenic efficiencies of UVA light treatment when applied to cells in buffer at high fluences, and to growing cells at low fluence rates, we propose that intrinsically the UVA-induced DNA damages are able to trigger the SOS response (cyclobutyl pyrimidine dimers and some O2-dependent lesions) but also constitute premutagenic sites (some lesions leading to alkali-labile DNA breaks).(ABSTRACT TRUNCATED AT 250 WORDS)

Bacterial Proteins

Ultraviolet light induction of skin carcinoma in the mouse; influence of cAMP modifying agents.

A short review of pathogenic factors in U.V. light skin carcinogenesis in the mouse is presented. Caffeine and theophylline applied locally during U.V. irradiation caused a 50 percent reduction of skin tumour induction in Swiss mice. These two chemicals are inhibitors of DNA postreplication repair, but they also raise the intracellular level of cyclic AMP by inhibiting cAMP phosphodiesterase with, as a consequence, a possible slowing down of cellular growth. Control experiments using three different chemicals capable of raising the cAMP level in epidermal cells gave negative results. These experimental data are compatible with our original hypothesis according to which production of skin cancers by U.V. radiation is in same way related to DNA repair which helps the cell to survive but allows or favours the occurrence of errors in cellular DNA.

Animals

Bright light induction of strong (type 0) resetting of the human circadian pacemaker.

The response of the human circadian pacemaker to light was measured in 45 resetting trials. Each trial consisted of an initial endogenous circadian phase assessment, a three-cycle stimulus which included 5 hours of bright light per cycle, and a final phase assessment. The stimulus induced strong (type 0) resetting, with responses highly dependent on the initial circadian phase of light exposure. The magnitude and direction of the phase shifts were modulated by the timing of exposure to ordinary room light, previously thought to be undetectable by the human pacemaker. The data indicate that the sensitivity of the human circadian pacemaker to light is far greater than previously recognized and have important implications for the therapeutic use of light in the management of disorders of circadian regulation.

Adult

Ultraviolet light induction of lambda from dcm host strains alleviates EcoRII restriction of phage.

A new form of restriction alleviation is demonstrated for phage induced by ultraviolet light from dcm strains of Escherichia coli K-12. EcoRII restriction of the induced phage is alleviated, which is the first report of Type II restriction alleviation. Unlike previously reported restriction alleviation, the increase in phage-plating efficiency is not dependent upon irradiation of the plating host for its induction.

Bacteriophage lambda

Ultraviolet light induction of peripheral granulocytosis with splenomegaly: protection of mice with topical p-aminobenzoic acid (PABA).

Hairless mice were exposed to UVB irradiation from a Philips T1 12 light source. Mice that were exposed to UV-light and not protected with 5% p-aminobenzoic acid (PABA) showed a significantly higher number of peripheral blood granulocytes (P less than 0.001) and a significantly higher mean weight of both the spleen and the liver (P less than 0.001) than the non-irradiated controls. Light microscopy of the histology of the enlarged liver and spleen showed a proliferation of granulocytes and the reticuloendothelial cells. Treatment with topical PABA during the whole period of UV-exposure prevented the peripheral blood granulocytosis. These protected mice also had a significantly (P less than 0.001) lower mean weight for the liver and spleen than UV-exposed and non-protected mice.

4-Aminobenzoic Acid

Sucrose mimics the light induction of Arabidopsis nitrate reductase gene transcription.

Nitrate reductase, the first enzyme in nitrate assimilation, is located at the crossroad of two energy-consuming pathways: nitrate assimilation and carbon fixation. Light, which regulates the expression of many higher-plant carbon fixation genes, also regulates nitrate reductase gene expression. Located in the cytosol, nitrate reductase obtains its reductant not from photosynthesis but from carbohydrate catabolism. This relationship prompted us to investigate the indirect role that light might play, via photosynthesis, in the regulation of nitrate reductase gene expression. We show that sucrose can replace light in eliciting an increase of nitrate reductase mRNA accumulation in dark-adapted green Arabidopsis plants. We show further that sucrose alone is sufficient for the full expression of nitrate reductase genes in etiolated Arabidopsis plants. Finally, using a reporter gene, we show that a 2.7-kilobase region of 5' flanking sequence of the nitrate reductase gene is sufficient to confer the light or the sucrose response.

Gene Expression

Blue light induction of conidiation-specific genes in Neurospora crassa.

The con genes of Neurospora crassa are preferentially expressed during a developmental process known as conidiation. We present evidence indicating that transcription of con-5 and con-10 is also stimulated by blue light. Transcription of these genes was not photoinducible in wc-1 and wc-2 mutant strains. The response of con-5 and con-10 to blue light was similar to that of al-1 and al-2, genes involved in carotenoid biosynthesis, and bli-3 and bli-4, blue light inducible genes.

Blotting, Northern

Cytokinin enhancement of the light induction of nitrate reductase transcript levels in etiolated barley leaves.

To investigate the molecular mechanism of cytokinin regulation of nitrate reductase (NR) activity, the influence of benzyladenine (BA) on the level of NR transcript was studied in etiolated barley leaves using a barley NR cDNA as a probe. Northern blot analyses of the levels of NR poly (A)+ RNA indicate that the amount present is proportional to the concentration of BA (2 x 10(-8) to 2 x 10(-4) M) applied to the leaves. Enhancement of NR mRNA by 2 x 10(-5) M BA was clearly detected after 15 minutes of exposure of the leaves to light. The enhancement is cytokinin-specific and adenine is ineffective. Brief treatment with the protein synthesis inhibitor, cycloheximide, inhibited BA-enhanced NR activity but did not inhibit BA-enhanced NR transcript level, thus the enhancement was independent of concurrent protein synthesis. Nuclear runoff transcription studies showed that the enhancement of NR mRNA was at least partially due to increased transcription rates.

Adenine

Ultraviolet light induction of diphtheria toxin-resistant mutants of normal and xeroderma pigmentosum human fibroblasts.

The UV induction of diphtheria toxin-resistant (DTr) mutants in normal and xeroderma pigmentosum human fibroblasts has been quantitatively characterized. A concentration of diphtheria toxin at which DTr cells are cross-resistant to Pseudomonas aeruginosa exotoxin A was determined and used in the selection of resistant mutants. Recovery of mutants was not influenced by the presence of wild-type cell densities of 1-8 x 10(5) per 9-cm plate, indicating no metabolic cooperation exists, in contrast to what is seen in the selection of some other variant phenotypes. Expression periods for UV-induced mutations differed with the severity of mutagen treatment and cell strain used. A relatively long (10-15 days after UV treatment) expression period was required for the maximum recovery of DTr mutants. Maximum recovery was followed by a decrease in mutation frequency on subsequent days evaluated. An apparent linear dose response within the dose range used was observed for UV-induced mutations in both normal and xeroderma pigmentosum fibroblasts. Our results indicate that xeroderma pigmentosum fibroblasts have higher UV-induced mutation frequencies per unit UV dose but similar frequencies per unit survival compared to normal cells within the range of UV doses tested.

Cells, Cultured