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Genomics Proteomics Bioinformatics ; 21(5): 950-961, 2023 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-37075831

RESUMEN

During mammalian preimplantation development, a totipotent zygote undergoes several cell cleavages and two rounds of cell fate determination, ultimately forming a mature blastocyst. Along with compaction, the establishment of apicobasal cell polarity breaks the symmetry of an embryo and guides subsequent cell fate choice. Although the lineage segregation of the inner cell mass (ICM) and trophectoderm (TE) is the first symbol of cell differentiation, several molecules have been shown to bias the early cell fate through their inter-cellular variations at much earlier stages, including the 2- and 4-cell stages. The underlying mechanisms of early cell fate determination have long been an important research topic. In this review, we summarize the molecular events that occur during early embryogenesis, as well as the current understanding of their regulatory roles in cell fate decisions. Moreover, as powerful tools for early embryogenesis research, single-cell omics techniques have been applied to both mouse and human preimplantation embryos and have contributed to the discovery of cell fate regulators. Here, we summarize their applications in the research of preimplantation embryos, and provide new insights and perspectives on cell fate regulation.


Asunto(s)
Blastocisto , Embrión de Mamíferos , Humanos , Animales , Ratones , Diferenciación Celular , Blastocisto/fisiología , Desarrollo Embrionario/genética , Cigoto , Linaje de la Célula/genética , Regulación del Desarrollo de la Expresión Génica , Mamíferos
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