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Pleomorphic Adenoma Gene 1 Is Needed For Timely Zygotic Genome Activation and Early Embryo Development

Pleomorphic adenoma gene 1 (PLAG1) is a transcription factor involved in cancer and growth. We discovered a de novo DNA motif containing a PLAG1 binding site in the promoters of genes activated during zygotic genome activation (ZGA) in human embryos. This motif was located within an Alu element in a...

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Autores principales: Madissoon, Elo, Damdimopoulos, Anastasios, Katayama, Shintaro, Krjutškov, Kaarel, Einarsdottir, Elisabet, Mamia, Katariina, De Groef, Bert, Hovatta, Outi, Kere, Juha, Damdimopoulou, Pauliina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6557853/
https://www.ncbi.nlm.nih.gov/pubmed/31182756
http://dx.doi.org/10.1038/s41598-019-44882-0
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author Madissoon, Elo
Damdimopoulos, Anastasios
Katayama, Shintaro
Krjutškov, Kaarel
Einarsdottir, Elisabet
Mamia, Katariina
De Groef, Bert
Hovatta, Outi
Kere, Juha
Damdimopoulou, Pauliina
author_facet Madissoon, Elo
Damdimopoulos, Anastasios
Katayama, Shintaro
Krjutškov, Kaarel
Einarsdottir, Elisabet
Mamia, Katariina
De Groef, Bert
Hovatta, Outi
Kere, Juha
Damdimopoulou, Pauliina
author_sort Madissoon, Elo
collection PubMed
description Pleomorphic adenoma gene 1 (PLAG1) is a transcription factor involved in cancer and growth. We discovered a de novo DNA motif containing a PLAG1 binding site in the promoters of genes activated during zygotic genome activation (ZGA) in human embryos. This motif was located within an Alu element in a region that was conserved in the murine B1 element. We show that maternally provided Plag1 is needed for timely mouse preimplantation embryo development. Heterozygous mouse embryos lacking maternal Plag1 showed disrupted regulation of 1,089 genes, spent significantly longer time in the 2-cell stage, and started expressing Plag1 ectopically from the paternal allele. The de novo PLAG1 motif was enriched in the promoters of the genes whose activation was delayed in the absence of Plag1. Further, these mouse genes showed a significant overlap with genes upregulated during human ZGA that also contain the motif. By gene ontology, the mouse and human ZGA genes with de novo PLAG1 motifs were involved in ribosome biogenesis and protein synthesis. Collectively, our data suggest that PLAG1 affects embryo development in mice and humans through a conserved DNA motif within Alu/B1 elements located in the promoters of a subset of ZGA genes.
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spelling pubmed-65578532019-06-19 Pleomorphic Adenoma Gene 1 Is Needed For Timely Zygotic Genome Activation and Early Embryo Development Madissoon, Elo Damdimopoulos, Anastasios Katayama, Shintaro Krjutškov, Kaarel Einarsdottir, Elisabet Mamia, Katariina De Groef, Bert Hovatta, Outi Kere, Juha Damdimopoulou, Pauliina Sci Rep Article Pleomorphic adenoma gene 1 (PLAG1) is a transcription factor involved in cancer and growth. We discovered a de novo DNA motif containing a PLAG1 binding site in the promoters of genes activated during zygotic genome activation (ZGA) in human embryos. This motif was located within an Alu element in a region that was conserved in the murine B1 element. We show that maternally provided Plag1 is needed for timely mouse preimplantation embryo development. Heterozygous mouse embryos lacking maternal Plag1 showed disrupted regulation of 1,089 genes, spent significantly longer time in the 2-cell stage, and started expressing Plag1 ectopically from the paternal allele. The de novo PLAG1 motif was enriched in the promoters of the genes whose activation was delayed in the absence of Plag1. Further, these mouse genes showed a significant overlap with genes upregulated during human ZGA that also contain the motif. By gene ontology, the mouse and human ZGA genes with de novo PLAG1 motifs were involved in ribosome biogenesis and protein synthesis. Collectively, our data suggest that PLAG1 affects embryo development in mice and humans through a conserved DNA motif within Alu/B1 elements located in the promoters of a subset of ZGA genes. Nature Publishing Group UK 2019-06-10 /pmc/articles/PMC6557853/ /pubmed/31182756 http://dx.doi.org/10.1038/s41598-019-44882-0 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Madissoon, Elo
Damdimopoulos, Anastasios
Katayama, Shintaro
Krjutškov, Kaarel
Einarsdottir, Elisabet
Mamia, Katariina
De Groef, Bert
Hovatta, Outi
Kere, Juha
Damdimopoulou, Pauliina
Pleomorphic Adenoma Gene 1 Is Needed For Timely Zygotic Genome Activation and Early Embryo Development
title Pleomorphic Adenoma Gene 1 Is Needed For Timely Zygotic Genome Activation and Early Embryo Development
title_full Pleomorphic Adenoma Gene 1 Is Needed For Timely Zygotic Genome Activation and Early Embryo Development
title_fullStr Pleomorphic Adenoma Gene 1 Is Needed For Timely Zygotic Genome Activation and Early Embryo Development
title_full_unstemmed Pleomorphic Adenoma Gene 1 Is Needed For Timely Zygotic Genome Activation and Early Embryo Development
title_short Pleomorphic Adenoma Gene 1 Is Needed For Timely Zygotic Genome Activation and Early Embryo Development
title_sort pleomorphic adenoma gene 1 is needed for timely zygotic genome activation and early embryo development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6557853/
https://www.ncbi.nlm.nih.gov/pubmed/31182756
http://dx.doi.org/10.1038/s41598-019-44882-0
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