Cloning, Tissue Expression, and Mapping of a Human Photolyase Homolog with Similarity to Plant Blue-Light Receptors

Enzymatic photoreactivation is a DNA repair mechanism that removes UV-induced pyrimidine dimer lesions by action of a single enzyme, photolyase, and visible light. Its presence has been demonstrated in a wide variety of organisms, ranging from simple prokaryotes to higher eukaryotes. We have isolate...

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Veröffentlicht in:Genomics (San Diego, Calif.) Calif.), 1996-10, Vol.37 (2), p.177-182
Hauptverfasser: Van Der Spek, P.J., Kobayashi, K., Bootsma, D., Takao, M., Eker, A.P.M., Yasui, A.
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Sprache:eng
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Zusammenfassung:Enzymatic photoreactivation is a DNA repair mechanism that removes UV-induced pyrimidine dimer lesions by action of a single enzyme, photolyase, and visible light. Its presence has been demonstrated in a wide variety of organisms, ranging from simple prokaryotes to higher eukaryotes. We have isolated a human gene encoding a 66-kDa protein that shows clear overall homology to known bacterial photolyase genes. The human gene product is more similar to plant blue-light receptors within class I photolyases than to higher eukaryote class II photolyases. Northern blot analysis showed two transcripts with constitutive expression in all tissues examined and an elevated expression in testis.In situhybridization with a cDNA-derived probe localized this human gene to chromosome 12q23–q24.1. Southern analysis of the cloned human gene suggests a wide distribution of the gene family in various species.
ISSN:0888-7543
1089-8646
DOI:10.1006/geno.1996.0539