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A program of successive gene expression in mouse one-cell embryos.
Asami, Maki; Lam, Brian Y H; Hoffmann, Martin; Suzuki, Toru; Lu, Xin; Yoshida, Naoko; Ma, Marcella K; Rainbow, Kara; Guzvic, Miodrag; VerMilyea, Matthew D; Yeo, Giles S H; Klein, Christoph A; Perry, Anthony C F.
Afiliación
  • Asami M; Laboratory of Mammalian Molecular Embryology, Department of Biology and Biochemistry, University of Bath, Bath BA2 7AY, UK.
  • Lam BYH; Medical Research Council (MRC) Metabolic Diseases Unit, Wellcome-MRC Institute of Metabolic Science-Metabolic Research Laboratories, Addenbrooke's Hospital, University of Cambridge, Cambridge CB2 0QQ, UK.
  • Hoffmann M; Project Group Personalized Tumor Therapy, Fraunhofer Institute for Toxicology and Experimental Medicine (ITEM), Regensburg, Germany.
  • Suzuki T; Laboratory of Mammalian Molecular Embryology, Department of Biology and Biochemistry, University of Bath, Bath BA2 7AY, UK.
  • Lu X; Experimental Medicine and Therapy Research, University of Regensburg, Regensburg, Germany.
  • Yoshida N; Department of Pathology, Kansai Medical University, Osaka 573-1010, Japan.
  • Ma MK; Medical Research Council (MRC) Metabolic Diseases Unit, Wellcome-MRC Institute of Metabolic Science-Metabolic Research Laboratories, Addenbrooke's Hospital, University of Cambridge, Cambridge CB2 0QQ, UK.
  • Rainbow K; Medical Research Council (MRC) Metabolic Diseases Unit, Wellcome-MRC Institute of Metabolic Science-Metabolic Research Laboratories, Addenbrooke's Hospital, University of Cambridge, Cambridge CB2 0QQ, UK.
  • Guzvic M; Experimental Medicine and Therapy Research, University of Regensburg, Regensburg, Germany.
  • VerMilyea MD; Embryology and Andrology Laboratories, Ovation Fertility Austin, Austin, TX 78731, USA.
  • Yeo GSH; Medical Research Council (MRC) Metabolic Diseases Unit, Wellcome-MRC Institute of Metabolic Science-Metabolic Research Laboratories, Addenbrooke's Hospital, University of Cambridge, Cambridge CB2 0QQ, UK. Electronic address: gshy2@cam.ac.uk.
  • Klein CA; Project Group Personalized Tumor Therapy, Fraunhofer Institute for Toxicology and Experimental Medicine (ITEM), Regensburg, Germany; Experimental Medicine and Therapy Research, University of Regensburg, Regensburg, Germany. Electronic address: christoph.klein@klinik.uni-regensburg.de.
  • Perry ACF; Laboratory of Mammalian Molecular Embryology, Department of Biology and Biochemistry, University of Bath, Bath BA2 7AY, UK. Electronic address: perry135@aol.com.
Cell Rep ; 42(2): 112023, 2023 02 28.
Article en En | MEDLINE | ID: mdl-36729835
At the moment of union in fertilization, sperm and oocyte are transcriptionally silent. The ensuing onset of embryonic transcription (embryonic genome activation [EGA]) is critical for development, yet its timing and profile remain elusive in any vertebrate species. We here dissect transcription during EGA by high-resolution single-cell RNA sequencing of precisely synchronized mouse one-cell embryos. This reveals a program of embryonic gene expression (immediate EGA [iEGA]) initiating within 4 h of fertilization. Expression during iEGA produces canonically spliced transcripts, occurs substantially from the maternal genome, and is mostly downregulated at the two-cell stage. Transcribed genes predict regulation by transcription factors (TFs) associated with cancer, including c-Myc. Blocking c-Myc or other predicted regulatory TF activities disrupts iEGA and induces acute developmental arrest. These findings illuminate intracellular mechanisms that regulate the onset of mammalian development and hold promise for the study of cancer.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Perfilación de la Expresión Génica / Embrión de Mamíferos Tipo de estudio: Prognostic_studies Idioma: En Revista: Cell Rep Año: 2023 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Perfilación de la Expresión Génica / Embrión de Mamíferos Tipo de estudio: Prognostic_studies Idioma: En Revista: Cell Rep Año: 2023 Tipo del documento: Article