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      Kick-starting the zygotic genome: licensors, specifiers, and beyond

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          Abstract

          Zygotic genome activation (ZGA), the first transcription event following fertilization, kickstarts the embryonic program that takes over the control of early development from the maternal products. How ZGA occurs, especially in mammals, is poorly understood due to the limited amount of research materials. With the rapid development of single-cell and low-input technologies, remarkable progress made in the past decade has unveiled dramatic transitions of the epigenomes, transcriptomes, proteomes, and metabolomes associated with ZGA. Moreover, functional investigations are yielding insights into the key regulators of ZGA, among which two major classes of players are emerging: licensors and specifiers. Licensors would control the permission of transcription and its timing during ZGA. Accumulating evidence suggests that such licensors of ZGA include regulators of the transcription apparatus and nuclear gatekeepers. Specifiers would instruct the activation of specific genes during ZGA. These specifiers include key transcription factors present at this stage, often facilitated by epigenetic regulators. Based on data primarily from mammals but also results from other species, we discuss in this review how recent research sheds light on the molecular regulation of ZGA and its executors, including the licensors and specifiers.

          Abstract

          How zygotic genome activation occurs in mammals is poorly understood. This review discusses how licensors set the stage for the initiation of transcription and its timing, and how specifiers, master transcription factors often coupled with epigenetic regulators, instruct the activation of specific genes.

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          Most cited references189

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          Regulation of chromatin by histone modifications.

          Chromatin is not an inert structure, but rather an instructive DNA scaffold that can respond to external cues to regulate the many uses of DNA. A principle component of chromatin that plays a key role in this regulation is the modification of histones. There is an ever-growing list of these modifications and the complexity of their action is only just beginning to be understood. However, it is clear that histone modifications play fundamental roles in most biological processes that are involved in the manipulation and expression of DNA. Here, we describe the known histone modifications, define where they are found genomically and discuss some of their functional consequences, concentrating mostly on transcription where the majority of characterisation has taken place.
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            The diverse roles of DNA methylation in mammalian development and disease

            DNA methylation is of paramount importance for mammalian embryonic development. DNA methylation has numerous functions: it is implicated in the repression of transposons and genes, but is also associated with actively transcribed gene bodies and, in some cases, with gene activation per se. In recent years, sensitive technologies have been developed that allow the interrogation of DNA methylation patterns from a small number of cells. The use of these technologies has greatly improved our knowledge of DNA methylation dynamics and heterogeneity in embryos and in specific tissues. Combined with genetic analyses, it is increasingly apparent that regulation of DNA methylation erasure and (re-)establishment varies considerably between different developmental stages. In this Review, we discuss the mechanisms and functions of DNA methylation and demethylation in both mice and humans at CpG-rich promoters, gene bodies and transposable elements. We highlight the dynamic erasure and re-establishment of DNA methylation in embryonic, germline and somatic cell development. Finally, we provide insights into DNA methylation gained from studying genetic diseases.
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              The Polycomb complex PRC2 and its mark in life.

              Polycomb group proteins maintain the gene-expression pattern of different cells that is set during early development by regulating chromatin structure. In mammals, two main Polycomb group complexes exist - Polycomb repressive complex 1 (PRC1) and 2 (PRC2). PRC1 compacts chromatin and catalyses the monoubiquitylation of histone H2A. PRC2 also contributes to chromatin compaction, and catalyses the methylation of histone H3 at lysine 27. PRC2 is involved in various biological processes, including differentiation, maintaining cell identity and proliferation, and stem-cell plasticity. Recent studies of PRC2 have expanded our perspectives on its function and regulation, and uncovered a role for non-coding RNA in the recruitment of PRC2 to target genes.
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                Author and article information

                Contributors
                xiewei121@tsinghua.edu.cn
                Journal
                EMBO Rep
                EMBO Rep
                EMBO Reports
                Nature Publishing Group UK (London )
                1469-221X
                1469-3178
                19 August 2024
                19 August 2024
                October 2024
                : 25
                : 10
                : 4113-4130
                Affiliations
                [1 ]Center for Stem Cell Biology and Regenerative Medicine, MOE Key Laboratory of Bioinformatics, School of Life Sciences, Tsinghua University, ( https://ror.org/03cve4549) 100084 Beijing, China
                [2 ]GRID grid.11135.37, ISNI 0000 0001 2256 9319, Peking University-Tsinghua University-National Institute of Biological Sciences (PTN) Joint Graduate Program, Academy for Advanced Interdisciplinary Studies, , Peking University, ; 100871 Beijing, China
                [3 ]Department of Biology, University of Pennsylvania, ( https://ror.org/00b30xv10) Philadelphia, PA USA
                [4 ]GRID grid.27860.3b, ISNI 0000 0004 1936 9684, Department of Microbiology and Molecular Genetics, College of Biological Sciences, , University of California, Davis, ; Davis, CA USA
                [5 ]GRID grid.452723.5, ISNI 0000 0004 7887 9190, Tsinghua-Peking Center for Life Sciences, ; Beijing, China
                Author information
                http://orcid.org/0000-0001-5923-6825
                http://orcid.org/0000-0003-2126-3849
                Article
                223
                10.1038/s44319-024-00223-5
                11467316
                39160344
                bdf7dd8a-6722-4eee-b7c1-08d145c956de
                © The Author(s) 2024

                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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. Creative Commons Public Domain Dedication waiver http://creativecommons.org/publicdomain/zero/1.0/ applies to the data associated with this article, unless otherwise stated in a credit line to the data, but does not extend to the graphical or creative elements of illustrations, charts, or figures. This waiver removes legal barriers to the re-use and mining of research data. According to standard scholarly practice, it is recommended to provide appropriate citation and attribution whenever technically possible.

                History
                : 10 February 2024
                : 14 June 2024
                : 24 July 2024
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001809, MOST | National Natural Science Foundation of China (NSFC);
                Award ID: 31988101
                Award ID: 31830047
                Award ID: 31725018
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100012166, MOST | National Key Research and Development Program of China (NKPs);
                Award ID: 2021YFA1100102
                Award ID: 2019YFA0508900
                Award Recipient :
                Funded by: Tsinghua-Peking Center for Life Sciences
                Funded by: FundRef http://dx.doi.org/10.13039/100000011, Howard Hughes Medical Institute (HHMI);
                Categories
                Review Article
                Custom metadata
                © European Molecular Biology Organization 2024

                Molecular biology
                zga,early embryo,licensor,specifier,transcription factor,chromatin, transcription & genomics,development

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