98%
921
2 minutes
20
Ultraviolet light induces photoproducts, cyclobutane pyrimidine dimers (CPDs) and (6-4) photoproducts (6-4PPs), in cellular DNA, which cause cytotoxic and genotoxic effects on the cells. Cells have several DNA repair mechanisms to repair the damage and to maintain genetic information of the cells. Photoreactivation is one of the DNA repair mechanism to remove UV-induced DNA damage from cellular DNA catalyzed by photolyase under visible light. Two types of photolyase, CPD photolyase and (6-4) photolyase, are specific for CPDs and for (6-4)PPs. We have isolated a gene product encoding CPD photolyase, named PHR2, from Dunaliella salina which is a kind of unicellular alga. Sequence analysis showed that PHR2 encodes a protein that has 529 amino acids and is similar to other Class II CPD photolyase. The complementation assay of the photoreactivation deficiency of the Escherichia coli SY2 by PHR2 cDNA showed a significant increase in survival rate when cells were irradiated with UV-C. Real-time PCR analysis indicated that the transcription of PHR2 was induced by UV-C, white light, high salinity, and H(2)O(2).
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.jphotobiol.2007.01.002 | DOI Listing |
Nat Commun
August 2025
Institute of Biological and Chemical Systems - Biological Information Processing, Karlsruhe Institute of Technology, Eggenstein-Leopoldshafen, Germany.
DNA damage is generated by various environmental stressors and so DNA repair systems must inevitably adapt to changing environments. Photolyases represent a highly conserved class of enzymes which repair UV-induced covalent crosslinks between adjacent pyrimidine bases (CPD and 6-4 photoproducts) via photoreactivation. In the blind cavefish Phreatichthys andruzzii which has evolved for millions of years completely isolated from UV radiation and visible light, we have documented multiple polymorphisms and loss of function mutations affecting both the 6-4phr and DASHphr photolyase genes while strangely, the CPDphr gene remains highly conserved.
View Article and Find Full Text PDFNucleic Acids Res
June 2025
School of Molecular Biosciences, Washington State University, Pullman, WA 99164, United States.
Ultraviolet (UV) light causes cyclobutane pyrimidine dimers (CPDs) and other DNA lesions that must be efficiently repaired to prevent cell death and mutagenesis. While mammals utilize the nucleotide excision repair (NER) pathway to repair CPDs, many species primarily utilize photolyase enzymes to repair UV damage. Our understanding of how different genomic and chromatin features impact photolyase repair across a eukaryotic genome is limited.
View Article and Find Full Text PDFJ Am Chem Soc
April 2025
Center for Ultrafast Science and Technology, School of Chemistry and Chemical Engineering, Zhangjiang Institute for Advanced Study, Shanghai Jiao Tong University, Shanghai 200240, China.
The class-II photolyases (PLs) are distantly related to the microbial class-I photolyases with low sequence similarity, yet they maintain a similar structural topology and repair the same UV-induced cyclobutane pyrimidine dimer (CPD). The class-I photolyases have been well characterized through a direct electron-transfer (ET) tunneling mechanism with high repair quantum yield, but such a mechanism seemingly does not apply to all of the members in the diversified photolyase family. Here, using femtosecond spectroscopy, we show our systematic characterization of CPD repair by the class-II photolyases from and and reveal their complete photocycles with determination of reaction times of all ten elementary steps, including seven electron-transfer processes.
View Article and Find Full Text PDFNutrients
February 2025
Department of Molecular Pathology, Tokyo Medical University, 6-1-1 Shinjyuku-ku, Tokyo 160-8402, Japan.
: Ultraviolet B (UV-B) is a significant risk factor for skin damage, as it induces cyclobutane pyrimidine dimers (CPD), which suppress DNA replication and transcription. Photolyase (PHR) is a blue light-dependent enzyme that repairs DNA damage caused by UV irradiation. While it is absent in human, it plays a crucial role in repairing CPD in other organisms.
View Article and Find Full Text PDFAppl Environ Microbiol
February 2025
Department of Microbiology and Immunology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Ultraviolet (UV) C light emitted by a krypton chloride (KrCl) lamp consists of mainly less harmful 222-nm Far-UVC (unfiltered 222-mm Far-UVC) compared with conventionally used 254-nm UVC. It also contains wavelengths that are harmful to mammalian cells. By contrast, UVC from a KrCl lamp with optical filter (filtered 222-nm Far-UVC) consists of much less harmful 222-nm Far-UVC and is available for sterilization of dwelling spaces.
View Article and Find Full Text PDF