哺乳類発生開始の新しいロードマップを提示(Roadmap for the start of human embryonic life)

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2025-08-08 バース大学

バース大学のMaki Asami博士とTony Perry教授らは、哺乳類の発生開始時における遺伝子活性化の時系列モデル「ロードマップ」を提示した。従来法では捉えにくかった受精直後の微弱な遺伝子発現を、高感度計測とケンブリッジ大学との共同研究により検出し、既存データと統合してモデル化。これにより、受精後すぐに遺伝子が活動を開始することが明らかになった。この知見は発生生物学の基礎理解を深めるだけでなく、不妊治療の改善や成人期疾患(がんなど)の起源解明にも寄与する可能性がある。

哺乳類発生開始の新しいロードマップを提示(Roadmap for the start of human embryonic life)
The researchers have created a roadmap of gene activity from the earliest moments after fertilisation.

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マウスとヒトの胚ゲノム活性化は1細胞期に開始される
Mouse and human embryonic genome activation initiate at the one-cell stage

Maki Asami,Anthony C. F. Perry
Frontiers in Cell and Developmental Biology   Published:30 July 2025
DOI:https://doi.org/10.3389/fcell.2025.1594995

At the moment of their union, fertilizing gametes (sperm and oocyte) are transcriptionally silent: gene expression has to be initiated within the resulting embryo, a process termed embryonic genome activation, EGA. Until recently, EGA was believed to occur at the two-cell stage (mouse) or four-to-eight-cell stage (human), but new evidence from single-cell RNA-sequencing (scRNAseq) suggests that it initiates at the one-cell stage in both species. Precise time-course scRNA-seq of mouse one-cell embryos revealed an EGA program referred to as immediate EGA, iEGA: iEGA occurred from within 4 h of fertilization, mainly from the maternal genome, with paternal genomic transcription from ∼10 h. Significant low-magnitude upregulation similarly occurred in healthy human one-cell embryos. In both species, new transcripts were canonically spliced, and expression predicted embryonic processes and regulatory transcription factors (TFs) associated with cancer, including MYC/c-Myc. Blocking their activities in mouse one-cell embryos induced acute developmental arrest and disrupted iEGA. Inhibiting c-Myc induced upregulation of hundreds of genes, implying that they are normatively repressed, a phenomenon we term embryonic genome repression, EGR. iEGA is downregulated coincidentally with a subsequent, higher-amplitude wave of gene expression (referred to as ‘major EGA’ or ‘major ZGA’) in two-cell (mouse) or 4–8-cell (human) embryos. We suggest that iEGA is continuous with gene expression previously termed ‘minor EGA’ (or ‘minor ZGA’) and that the regulation of iEGA and major EGA are distinctive. The pattern of gene upregulation in iEGA illuminates processes involved at the onset of development, with implications for epigenetic inheritance, stem cell-derived embryos and cancer.

細胞遺伝子工学
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