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Targeted gene disruption by use of transcription activator-like effector nuclease (TALEN) in the water flea Daphnia pulex

BACKGROUND: The cosmopolitan microcrustacean Daphnia pulex provides a model system for both human health research and monitoring ecosystem integrity. It is the first crustacean to have its complete genome sequenced, an unprecedented ca. 36% of which has no known homologs with any other species. More...

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Autores principales: Hiruta, Chizue, Ogino, Yukiko, Sakuma, Tetsushi, Toyota, Kenji, Miyagawa, Shinichi, Yamamoto, Takashi, Iguchi, Taisen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4239399/
https://www.ncbi.nlm.nih.gov/pubmed/25404042
http://dx.doi.org/10.1186/s12896-014-0095-7
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author Hiruta, Chizue
Ogino, Yukiko
Sakuma, Tetsushi
Toyota, Kenji
Miyagawa, Shinichi
Yamamoto, Takashi
Iguchi, Taisen
author_facet Hiruta, Chizue
Ogino, Yukiko
Sakuma, Tetsushi
Toyota, Kenji
Miyagawa, Shinichi
Yamamoto, Takashi
Iguchi, Taisen
author_sort Hiruta, Chizue
collection PubMed
description BACKGROUND: The cosmopolitan microcrustacean Daphnia pulex provides a model system for both human health research and monitoring ecosystem integrity. It is the first crustacean to have its complete genome sequenced, an unprecedented ca. 36% of which has no known homologs with any other species. Moreover, D. pulex is ideally suited for experimental manipulation because of its short reproductive cycle, large numbers of offspring, synchronization of oocyte maturation, and other life history characteristics. However, existing gene manipulation techniques are insufficient to accurately define gene functions. Although our previous investigations developed an RNA interference (RNAi) system in D. pulex, the possible time period of functional analysis was limited because the effectiveness of RNAi is transient. Thus, in this study, we developed a genome editing system for D. pulex by first microinjecting transcription activator-like effector nuclease (TALEN) mRNAs into early embryos and then evaluating TALEN activity and mutation phenotypes. RESULTS: We assembled a TALEN construct specific to the Distal-less gene (Dll), which is a homeobox transcription factor essential for distal limb development in invertebrates and vertebrates, and evaluated its activity in vitro by single-strand annealing assay. Then, we injected TALEN mRNAs into eggs within 1 hour post-ovulation. Injected embryos presented with defects in the second antenna and altered appendage development, and indel mutations were detected in Dll loci, indicating that this technique successfully knocked out the target gene. CONCLUSIONS: We succeeded, for the first time in D. pulex, in targeted mutagenesis by use of Platinum TALENs. This genome editing technique makes it possible to conduct reverse genetic analysis in D. pulex, making this species an even more appropriate model organism for environmental, evolutionary, and developmental genomics. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12896-014-0095-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-42393992014-11-21 Targeted gene disruption by use of transcription activator-like effector nuclease (TALEN) in the water flea Daphnia pulex Hiruta, Chizue Ogino, Yukiko Sakuma, Tetsushi Toyota, Kenji Miyagawa, Shinichi Yamamoto, Takashi Iguchi, Taisen BMC Biotechnol Methodology Article BACKGROUND: The cosmopolitan microcrustacean Daphnia pulex provides a model system for both human health research and monitoring ecosystem integrity. It is the first crustacean to have its complete genome sequenced, an unprecedented ca. 36% of which has no known homologs with any other species. Moreover, D. pulex is ideally suited for experimental manipulation because of its short reproductive cycle, large numbers of offspring, synchronization of oocyte maturation, and other life history characteristics. However, existing gene manipulation techniques are insufficient to accurately define gene functions. Although our previous investigations developed an RNA interference (RNAi) system in D. pulex, the possible time period of functional analysis was limited because the effectiveness of RNAi is transient. Thus, in this study, we developed a genome editing system for D. pulex by first microinjecting transcription activator-like effector nuclease (TALEN) mRNAs into early embryos and then evaluating TALEN activity and mutation phenotypes. RESULTS: We assembled a TALEN construct specific to the Distal-less gene (Dll), which is a homeobox transcription factor essential for distal limb development in invertebrates and vertebrates, and evaluated its activity in vitro by single-strand annealing assay. Then, we injected TALEN mRNAs into eggs within 1 hour post-ovulation. Injected embryos presented with defects in the second antenna and altered appendage development, and indel mutations were detected in Dll loci, indicating that this technique successfully knocked out the target gene. CONCLUSIONS: We succeeded, for the first time in D. pulex, in targeted mutagenesis by use of Platinum TALENs. This genome editing technique makes it possible to conduct reverse genetic analysis in D. pulex, making this species an even more appropriate model organism for environmental, evolutionary, and developmental genomics. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12896-014-0095-7) contains supplementary material, which is available to authorized users. BioMed Central 2014-11-18 /pmc/articles/PMC4239399/ /pubmed/25404042 http://dx.doi.org/10.1186/s12896-014-0095-7 Text en © Hiruta et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Methodology Article
Hiruta, Chizue
Ogino, Yukiko
Sakuma, Tetsushi
Toyota, Kenji
Miyagawa, Shinichi
Yamamoto, Takashi
Iguchi, Taisen
Targeted gene disruption by use of transcription activator-like effector nuclease (TALEN) in the water flea Daphnia pulex
title Targeted gene disruption by use of transcription activator-like effector nuclease (TALEN) in the water flea Daphnia pulex
title_full Targeted gene disruption by use of transcription activator-like effector nuclease (TALEN) in the water flea Daphnia pulex
title_fullStr Targeted gene disruption by use of transcription activator-like effector nuclease (TALEN) in the water flea Daphnia pulex
title_full_unstemmed Targeted gene disruption by use of transcription activator-like effector nuclease (TALEN) in the water flea Daphnia pulex
title_short Targeted gene disruption by use of transcription activator-like effector nuclease (TALEN) in the water flea Daphnia pulex
title_sort targeted gene disruption by use of transcription activator-like effector nuclease (talen) in the water flea daphnia pulex
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4239399/
https://www.ncbi.nlm.nih.gov/pubmed/25404042
http://dx.doi.org/10.1186/s12896-014-0095-7
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