Kravchenko Pavel, Tachibana Kikuë
Department of Totipotency, Max Planck Institute of Biochemistry, Munich, Germany.
Nat Rev Mol Cell Biol. 2025 Jan;26(1):68-79. doi: 10.1038/s41580-024-00772-6. Epub 2024 Oct 2.
In sexually reproducing organisms, life begins with the fusion of transcriptionally silent gametes, the oocyte and sperm. Although initiation of transcription in the embryo, known as zygotic genome activation (ZGA), is universally required for development, the transcription factors regulating this process are poorly conserved. In this Perspective, we discuss recent insights into the mechanisms of ZGA in totipotent mammalian embryos, namely ZGA regulation by several transcription factors, including by orphan nuclear receptors (OrphNRs) such as the pioneer transcription factor NR5A2, and by factors of the DUX, TPRX and OBOX families. We performed a meta-analysis and compiled a list of pan-ZGA genes, and found that most of these genes are indeed targets of the above transcription factors. Remarkably, more than a third of these ZGA genes appear to be regulated both by OrphNRs such as NR5A2 and by OBOX proteins, whose motifs co-occur in SINE B1 retrotransposable elements, which are enriched near ZGA genes. We propose that ZGA in mice is activated by recruitment of multiple transcription factors to SINE B1 elements that function as enhancers, and discuss a potential relevance of this mechanism to Alu retrotransposable elements in human ZGA.
在有性生殖的生物体中,生命始于转录沉默的配子——卵母细胞和精子的融合。尽管胚胎中的转录起始,即合子基因组激活(ZGA),是发育普遍所需的,但调节这一过程的转录因子在进化上保守性较差。在这篇观点文章中,我们讨论了对全能哺乳动物胚胎中ZGA机制的最新见解,即ZGA受多种转录因子的调控,包括孤儿核受体(OrphNRs),如先锋转录因子NR5A2,以及DUX、TPRX和OBOX家族的因子。我们进行了一项荟萃分析并编制了一份泛ZGA基因列表,发现这些基因中的大多数确实是上述转录因子的靶标。值得注意的是,这些ZGA基因中有超过三分之一似乎同时受NR5A2等OrphNRs和OBOX蛋白的调控,它们的基序共同出现在SINE B1逆转座子元件中,这些元件在ZGA基因附近富集。我们提出,小鼠中的ZGA是通过多种转录因子被招募到作为增强子的SINE B1元件上而被激活的,并讨论了这一机制与人类ZGA中的Alu逆转座子元件的潜在相关性。