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1.
Eukaryot Cell ; 6(9): 1682-92, 2007 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-17545314

RESUMEN

The photolyases, DNA repair enzymes that use visible and long-wavelength UV light to repair cyclobutane pyrimidine dimers (CPDs) created by short-wavelength UV, belong to the larger photolyase-cryptochrome gene family. Cryptochromes (UVA-blue light photoreceptors) lack repair activity, and sensory and regulatory roles have been defined for them in plants and animals. Evolutionary considerations indicate that cryptochromes diverged from CPD photolyases before the emergence of eukaryotes. In prokaryotes and lower eukaryotes, some photolyases might have photosensory functions. phr1 codes for a class I CPD photolyase in Trichoderma atroviride. phr1 is rapidly induced by blue and UVA light, and its photoinduction requires functional blue light regulator (BLR) proteins, which are White Collar homologs in Trichoderma. Here we show that deletion of phr1 abolished photoreactivation of UVC (200 to 280 nm)-inhibited spores and thus that PHR1 is the main component of the photorepair system. The 2-kb 5' upstream region of phr1, with putative light-regulated elements, confers blue light regulation on a reporter gene. To assess phr1 photosensory function, fluence response curves of this light-regulated promoter were tested in null mutant (Deltaphr1) strains. Photoinduction of the phr1 promoter in Deltaphr1 strains was >5-fold more sensitive to light than that in the wild type, whereas in PHR1-overexpressing lines the sensitivity to light increased about 2-fold. Our data suggest that PHR1 may regulate its expression in a light-dependent manner, perhaps through negative modulation of the BLR proteins. This is the first evidence for a regulatory role of photolyase, a role usually attributed to cryptochromes.


Asunto(s)
Desoxirribodipirimidina Fotoliasa/genética , Proteínas Fúngicas/genética , Regulación Fúngica de la Expresión Génica , Homeostasis , Trichoderma/enzimología , Secuencia de Aminoácidos , Criptocromos , Reparación del ADN , Desoxirribodipirimidina Fotoliasa/fisiología , Flavoproteínas/metabolismo , Proteínas Fúngicas/fisiología , Eliminación de Gen , Expresión Génica/efectos de la radiación , Proteínas Fluorescentes Verdes/análisis , Proteínas Fluorescentes Verdes/genética , Datos de Secuencia Molecular , Regiones Promotoras Genéticas/efectos de la radiación , Trichoderma/genética , Trichoderma/efectos de la radiación , Rayos Ultravioleta
2.
J Biol Chem ; 278(40): 39143-54, 2003 Oct 03.
Artículo en Inglés | MEDLINE | ID: mdl-12878596

RESUMEN

The sequence of Vibrio cholerae genome revealed three genes belonging to the photolyase/cryptochrome blue-light photoreceptor family. The proteins encoded by the three genes were purified and characterized. All three proteins contain folate and flavin cofactors and have absorption peaks in the range of 350-500 nm. Only one of the three, VcPhr, is a photolyase specific for cyclobutane pyrimidine dimers. The other two are cryptochromes and were designated VcCry1 and VcCry2, respectively. Mutation of phr abolishes photoreactivation of UV-induced killing, whereas mutations in cry1 and cry2 do not affect photorepair activity. VcCry1 exhibits some unique features. Of all cryptochromes characterized to date, it is the only one that contains stoichiometric amounts of both chromophores and retains its flavin cofactor in the two-electron reduced FADH2 form. In addition, VcCry1 exhibits RNA binding activity and co-purifies with an RNA of 60-70 nucleotides in length.


Asunto(s)
Desoxirribodipirimidina Fotoliasa/química , Proteínas de Drosophila , Proteínas del Ojo , Flavina-Adenina Dinucleótido/análogos & derivados , Flavoproteínas/química , Células Fotorreceptoras de Invertebrados , Células Fotorreceptoras/química , Vibrio cholerae/metabolismo , Secuencia de Aminoácidos , Clonación Molecular , Criptocromos , Desoxirribodipirimidina Fotoliasa/aislamiento & purificación , Dimerización , Relación Dosis-Respuesta en la Radiación , Electroforesis en Gel de Poliacrilamida , Escherichia coli/metabolismo , Flavina-Adenina Dinucleótido/química , Flavoproteínas/aislamiento & purificación , Calor , Ligandos , Luz , Datos de Secuencia Molecular , Mutación , Plásmidos/metabolismo , ARN/metabolismo , Receptores Acoplados a Proteínas G , Homología de Secuencia de Aminoácido , Espectrometría de Fluorescencia , Espectrofotometría , Rayos Ultravioleta
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