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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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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 |
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author | 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 |
author_facet | 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 |
author_sort | Franz, Sophie |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6125616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61256162018-09-11 Structure of the bifunctional cryptochrome aCRY from Chlamydomonas reinhardtii 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 Nucleic Acids Res Structural Biology 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. Oxford University Press 2018-09-06 2018-07-19 /pmc/articles/PMC6125616/ /pubmed/30032195 http://dx.doi.org/10.1093/nar/gky621 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Structural Biology 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 Structure of the bifunctional cryptochrome aCRY from Chlamydomonas reinhardtii |
title | Structure of the bifunctional cryptochrome aCRY from Chlamydomonas reinhardtii |
title_full | Structure of the bifunctional cryptochrome aCRY from Chlamydomonas reinhardtii |
title_fullStr | Structure of the bifunctional cryptochrome aCRY from Chlamydomonas reinhardtii |
title_full_unstemmed | Structure of the bifunctional cryptochrome aCRY from Chlamydomonas reinhardtii |
title_short | Structure of the bifunctional cryptochrome aCRY from Chlamydomonas reinhardtii |
title_sort | structure of the bifunctional cryptochrome acry from chlamydomonas reinhardtii |
topic | Structural Biology |
url | 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 |
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