ALFALFA SEEDLINGS GROWN OUTDOORS ARE MORE RESISTANT TO UV‐INDUCED DNA DAMAGE THAN PLANTS GROWN IN A UV‐FREE ENVIRONMENTAL CHAMBER

Abstract The relative UV sensitivities of alfalfa seedlings grown outdoors versus plants grown in a growth chamber under UV‐filtered cool white fluorescent bulbs have been determined using three criteria: (1) level of endogenous DNA damage as sites for the UV endonuclease from Micrococcus luteus. (2) susceptibility to pyrimidine dimer induction by a UV challenge exposure and (3) ability to repair UV‐induced damage. We find that outdoor‐grown plants contain approximately equal frequencies of endogenous DNA damages, are less susceptible to dimer induction by a challenge exposure of broad‐spectrum UV and photorepair dimers more rapidly than plants grown in an environmental chamber under cool white fluorescent lamps plus a filter that removes most UV radiation. These data suggest that plants grown in a natural environment would be less sensitive to UVB‐induced damage than would be predicted on the basis of studies on plants grown under minimum UV.

[1]  A. Stapleton,et al.  Flavonoids Can Protect Maize DNA from the Induction of Ultraviolet Radiation Damage , 1994, Plant physiology.

[2]  J. Sutherland,et al.  Quantitation of supercoiled DNA cleavage in nonradioactive DNA: application to ionizing radiation and synthetic endonuclease cleavage. , 1992, Analytical biochemistry.

[3]  A. Takahashi,et al.  Light-Induced Anthocyanin Reduces the Extent of Damage to DNA in UV-Irradiated Centaurea cyanus Cells in Culture , 1991 .

[4]  B. Langer,et al.  PHYTOCHROME INDUCTION OF PHOTOREACTIVATING ENZYME IN Phaseolus vulgaris L. SEEDLINGS* , 1990 .

[5]  J. Sutherland,et al.  Electronic imaging system for direct and rapid quantitation of fluorescence from electrophoretic gels: application to ethidium bromide-stained DNA. , 1987, Analytical biochemistry.

[6]  J. Sutherland,et al.  Unidirectional pulsed-field electrophoresis of single- and double-stranded DNA in agarose gels: analytical expressions relating mobility and molecular length and their application in the measurement of strand breaks. , 1987, Analytical biochemistry.

[7]  J C Sutherland,et al.  Quantitation of radiation-, chemical-, or enzyme-induced single strand breaks in nonradioactive DNA by alkaline gel electrophoresis: application to pyrimidine dimers. , 1986, Analytical biochemistry.

[8]  A. Rauth,et al.  COMPARISON OF SPECTRAL PURITY AND INTENSITY OF DIFFERENT U.V. MONOCHROMATORS , 1965 .

[9]  A. Rauth,et al.  THEORY AND DESIGN OF HIGH INTENSITY U.V MONOCHROMATORS FOR PHOTOBIOLOGY AND PHOTOCHEMISTRY , 1965 .

[10]  J. Jagger A small and inexpensive ultraviolet dose-rate meter useful in biological experiements. , 1961, Radiation research.

[11]  J. C. Sutherland,et al.  Action spectrum for DMA damage in alfalfa lowers predicted impact of ozone depletion , 1992, Nature.

[12]  F. E. Quaite,et al.  Quantitation of pyrimidine dimers in DNA from UVB-irradiated alfalfa (Medicago sativa L.) seedlings. , 1992, Applied and theoretical electrophoresis : the official journal of the International Electrophoresis Society.

[13]  C. S. Rupert,et al.  Analaysis of photoenzymatic repair of UV lesions in DNA by single light flashes. XI. Light-induced activation of the yeast photoreactivating enzyme. , 1976, Mutation research.