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Structure of the bifunctional cryptochrome aCRY from Chlamydomonas reinhardtii

Photolyases and cryptochromes form an almost ubiquitous family of blue light photoreceptors involved in the repair and maintenance of DNA integrity or regulatory control. We found that one cryptochrome from the green alga Chlamydomonas reinhardtii (CraCRY) is capable of both, control of transcript l...

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Detalles Bibliográficos
Autores principales: Franz, Sophie, Ignatz, Elisabeth, Wenzel, Sandra, Zielosko, Hannah, Putu, Eka Putra Gusti Ngurah, Maestre-Reyna, Manuel, Tsai, Ming-Daw, Yamamoto, Junpei, Mittag, Maria, Essen, Lars-Oliver
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125616/
https://www.ncbi.nlm.nih.gov/pubmed/30032195
http://dx.doi.org/10.1093/nar/gky621
Descripción
Sumario:Photolyases and cryptochromes form an almost ubiquitous family of blue light photoreceptors involved in the repair and maintenance of DNA integrity or regulatory control. We found that one cryptochrome from the green alga Chlamydomonas reinhardtii (CraCRY) is capable of both, control of transcript levels and the sexual cycle of the alga in a positive (germination) and negative manner (mating ability), as well as catalyzing the repair of UV-DNA lesions. Its 1.6 Å crystal structure shows besides the FAD chromophore an aromatic tetrad that is indispensable in animal-like type I cryptochromes for light-driven change of their signaling-active redox state and formation of a stable radical pair. Given CraCRY’s catalytic activity as (6-4) photolyase in vivo and in vitro, we present the first co-crystal structure of a cryptochrome with duplex DNA comprising a (6-4) pyrimidine–pyrimidone lesion. This 2.9 Å structure reveals a distinct conformation for the catalytic histidine His(1), H357, that challenges previous models of a single-photon driven (6-4) photolyase mechanism.