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Non-base-contacting residues enable kaleidoscopic evolution of metazoan C2H2 zinc finger DNA binding

BACKGROUND: The C2H2 zinc finger (C2H2-ZF) is the most numerous protein domain in many metazoans, but is not as frequent or diverse in other eukaryotes. The biochemical and evolutionary mechanisms that underlie the diversity of this DNA-binding domain exclusively in metazoans are, however, mostly un...

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Autores principales: Najafabadi, Hamed S., Garton, Michael, Weirauch, Matthew T., Mnaimneh, Sanie, Yang, Ally, Kim, Philip M., Hughes, Timothy R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5588721/
https://www.ncbi.nlm.nih.gov/pubmed/28877740
http://dx.doi.org/10.1186/s13059-017-1287-y
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author Najafabadi, Hamed S.
Garton, Michael
Weirauch, Matthew T.
Mnaimneh, Sanie
Yang, Ally
Kim, Philip M.
Hughes, Timothy R.
author_facet Najafabadi, Hamed S.
Garton, Michael
Weirauch, Matthew T.
Mnaimneh, Sanie
Yang, Ally
Kim, Philip M.
Hughes, Timothy R.
author_sort Najafabadi, Hamed S.
collection PubMed
description BACKGROUND: The C2H2 zinc finger (C2H2-ZF) is the most numerous protein domain in many metazoans, but is not as frequent or diverse in other eukaryotes. The biochemical and evolutionary mechanisms that underlie the diversity of this DNA-binding domain exclusively in metazoans are, however, mostly unknown. RESULTS: Here, we show that the C2H2-ZF expansion in metazoans is facilitated by contribution of non-base-contacting residues to DNA binding energy, allowing base-contacting specificity residues to mutate without catastrophic loss of DNA binding. In contrast, C2H2-ZF DNA binding in fungi, plants, and other lineages is constrained by reliance on base-contacting residues for DNA-binding functionality. Reconstructions indicate that virtually every DNA triplet was recognized by at least one C2H2-ZF domain in the common progenitor of placental mammals, but that extant C2H2-ZF domains typically bind different sequences from these ancestral domains, with changes facilitated by non-base-contacting residues. CONCLUSIONS: Our results suggest that the evolution of C2H2-ZFs in metazoans was expedited by the interaction of non-base-contacting residues with the DNA backbone. We term this phenomenon “kaleidoscopic evolution,” to reflect the diversity of both binding motifs and binding motif transitions and the facilitation of their diversification. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-017-1287-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-55887212017-09-14 Non-base-contacting residues enable kaleidoscopic evolution of metazoan C2H2 zinc finger DNA binding Najafabadi, Hamed S. Garton, Michael Weirauch, Matthew T. Mnaimneh, Sanie Yang, Ally Kim, Philip M. Hughes, Timothy R. Genome Biol Research BACKGROUND: The C2H2 zinc finger (C2H2-ZF) is the most numerous protein domain in many metazoans, but is not as frequent or diverse in other eukaryotes. The biochemical and evolutionary mechanisms that underlie the diversity of this DNA-binding domain exclusively in metazoans are, however, mostly unknown. RESULTS: Here, we show that the C2H2-ZF expansion in metazoans is facilitated by contribution of non-base-contacting residues to DNA binding energy, allowing base-contacting specificity residues to mutate without catastrophic loss of DNA binding. In contrast, C2H2-ZF DNA binding in fungi, plants, and other lineages is constrained by reliance on base-contacting residues for DNA-binding functionality. Reconstructions indicate that virtually every DNA triplet was recognized by at least one C2H2-ZF domain in the common progenitor of placental mammals, but that extant C2H2-ZF domains typically bind different sequences from these ancestral domains, with changes facilitated by non-base-contacting residues. CONCLUSIONS: Our results suggest that the evolution of C2H2-ZFs in metazoans was expedited by the interaction of non-base-contacting residues with the DNA backbone. We term this phenomenon “kaleidoscopic evolution,” to reflect the diversity of both binding motifs and binding motif transitions and the facilitation of their diversification. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-017-1287-y) contains supplementary material, which is available to authorized users. BioMed Central 2017-09-06 /pmc/articles/PMC5588721/ /pubmed/28877740 http://dx.doi.org/10.1186/s13059-017-1287-y Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Najafabadi, Hamed S.
Garton, Michael
Weirauch, Matthew T.
Mnaimneh, Sanie
Yang, Ally
Kim, Philip M.
Hughes, Timothy R.
Non-base-contacting residues enable kaleidoscopic evolution of metazoan C2H2 zinc finger DNA binding
title Non-base-contacting residues enable kaleidoscopic evolution of metazoan C2H2 zinc finger DNA binding
title_full Non-base-contacting residues enable kaleidoscopic evolution of metazoan C2H2 zinc finger DNA binding
title_fullStr Non-base-contacting residues enable kaleidoscopic evolution of metazoan C2H2 zinc finger DNA binding
title_full_unstemmed Non-base-contacting residues enable kaleidoscopic evolution of metazoan C2H2 zinc finger DNA binding
title_short Non-base-contacting residues enable kaleidoscopic evolution of metazoan C2H2 zinc finger DNA binding
title_sort non-base-contacting residues enable kaleidoscopic evolution of metazoan c2h2 zinc finger dna binding
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5588721/
https://www.ncbi.nlm.nih.gov/pubmed/28877740
http://dx.doi.org/10.1186/s13059-017-1287-y
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