bims-mazytr Biomed News
on Maternal‐to‐zygotic transition
Issue of 2025–05–11
three papers selected by
川一刀



  1. J Reprod Dev. 2025 May 03.
      During mouse preimplantation development, zygotic genome activation (ZGA), which synthesizes new transcripts in the embryo, occurs during the 1-cell to 2-cell stage. Embryos at the 1- and 2-cell stages are totipotent, and as embryonic development progresses, their differentiation potential decreases, and the embryos become pluripotent. However, the roles of genes expressed during ZGA in mouse embryonic differentiation remain incompletely understood. Here, we show that periodic tryptophan protein 1 (Pwp1), a WD-repeat protein, is expressed from the ZGA and controls embryonic differentiation at later stages. Developmental potential was reduced when siRNAs or antisense oligonucleotides targeting Pwp1 were introduced into 1-cell stage mouse embryos. Further, Pwp1 knockdown resulted in irregular localization of YAP1 at the morula stage, upregulation of the inner cell mass marker Nanog, and downregulation of the trophectoderm marker Cdx2 at the blastocyst stage. Transcriptome analysis showed that Pwp1 knockdown upregulated ZGA gene expression at the morula stage. Because Pwp1 contributes to H4K20me3 histone modification, these results suggest that Pwp1 is required for mouse preimplantation development to control differentiation-associated genes via H4K20me3 modification. Elucidating the role of Pwp1 in embryonic differentiation is expected to contribute toward the advancement of assisted reproductive technologies.
    Keywords:  Antisense oligonucleotide; Mouse preimplantation embryos; PWP1; siRNA
    DOI:  https://doi.org/10.1262/jrd.2024-111
  2. Genome Biol. 2025 May 08. 26(1): 120
       BACKGROUND: During meiosis, the oocyte genome keeps dormant for a long time until zygotic genome activation. The dynamics and homeostasis of the maternal transcriptome are essential for maternal-to-zygotic transition. Zygotic arrest 1 (ZAR1) and its homolog, ZAR2, are RNA-binding proteins that are important for the regulation of maternal mRNA stability.
    RESULTS: Smart-seq2 analysis reveals drastically downregulated maternal transcripts. However, the detection of transcript levels by Smart-seq2 may be biased by the polyadenylated tail length of the mRNAs. Similarly, differential expression of maternal transcripts in oocytes with or without Zar1/2 differs when analyzed using total RNA-seq and Smart-seq2, suggesting an influence of polyadenylation. Combined analyses using total RNA-seq, LACE-seq, PAIso-seq2, and immunoprecipitation-mass spectrometry reveals that ZAR1 may target the 3'-untranslated regions of maternal transcripts, regulates their stability in germinal vesicle stage oocytes, and interacts with other proteins to control the polyadenylation of mRNAs.
    CONCLUSIONS: The jointly analyzed multi-omics data highlight the limitations of Smart-seq2 in oocytes, clarify the dynamics of the maternal transcriptome, and uncover new roles of ZAR1 in regulating the maternal transcriptome.
    Keywords:  Maternal-to-zygotic transition; Meiosis; Oocyte transcriptome; RNA polyadenylation; RNA-binding proteins
    DOI:  https://doi.org/10.1186/s13059-025-03593-8
  3. Biol Reprod. 2025 May 03. pii: ioaf098. [Epub ahead of print]
      Previous murine studies have established that large-scale chromatin modifications upon completion of oocyte growth are associated with nucleolar transcriptional silencing. These modifications seem essential both for completion of the oocyte's meiosis and subsequent embryonic developmental success. Investigating this putative interconnection between nucleolar transcriptional activity and spatial chromatin organization towards completion of oocyte growth in pigs, we scrutinized whether 3D chromatin organization and heterochromatin localization, along with epigenetic markers, could indicate oocyte quality and predict developmental competence of harvested porcine oocytes. Supravital brilliant-cresyl-blue (BCB) staining was used to classify porcine cumulus-oocyte-complexes (COCs) as fully grown (BCB+) or still growing (BCB-). Oocytes were analyzed via integrated 3D-immunofluorescence for nucleolar activity and heterochromatin markers, as well as 3D-DNA-FISH for specific heterochromatin sequences. Additionally, some oocytes were prepared for transmission electron microscopy (TEM). TEM revealed distinct ultrastructural differences between BCB+ and BCB- oocytes and validated BCB-staining as viable method for a rough assessment of oocyte developmental competence. Immunostaining identified all known germinal vesicle (GV) chromatin configurations (non-surrounded nucleolus (NSN), partially non-surrounded nucleolus (pNSN), partially surrounded nucleolus (pSN), surrounded nucleolus (SN)) and linked them to respective BCB categories. Nucleolar activity was detected only in NSN oocytes, predominantly from the BCB- group. Protein markers and FISH signals revealed significant 3D-organizational changes in chromatin between NSN and SN conformations, clustering around the nucleolus towards final oocyte maturation. These findings highlight an evident interconnection between nucleolar transcriptional silencing and specific 3D chromatin organization patterns, with changes in heterochromatin localization indicating completion of the oocytes' growth phase and marking higher competency for subsequent final maturation and embryonic development.
    Keywords:  Brilliant cresyl blue; Chromatin conformation; Epigenetics; Nucleolar sphere; Oocyte developmental biology; Pericentromeric satellite dna; Porcine oocytes; Transcriptional activity
    DOI:  https://doi.org/10.1093/biolre/ioaf098