Zygotic Splicing Activation of the Transcriptome is a Crucial Aspect of Maternal-to-Zygotic Transition and Required for the Conversion from Totipotency to Pluripotency

Adv Sci (Weinh). 2024 Apr;11(14):e2308496. doi: 10.1002/advs.202308496. Epub 2024 Feb 2.

Abstract

During maternal-to-zygotic transition (MZT) in the embryo, mRNA undergoes complex post-transcriptional regulatory processes. However, it is unclear whether and how alternative splicing plays a functional role in MZT. By analyzing transcriptome changes in mouse and human early embryos, dynamic changes in alternative splicing during MZT are observed and a previously unnoticed process of zygotic splicing activation (ZSA) following embryonic transcriptional activation is described. As the underlying mechanism of RNA splicing, splicing factors undergo dramatic maternal-to-zygotic conversion. This conversion relies on the key maternal factors BTG4 and PABPN1L and is zygotic-transcription-dependent. CDK11-dependent phosphorylation of the key splicing factor, SF3B1, and its aggregation with SRSF2 in the subnuclear domains of 2-cell embryos are prerequisites for ZSA. Isoforms generated by erroneous splicing, such as full-length Dppa4, hinder normal embryonic development. Moreover, alternative splicing regulates the conversion of early embryonic blastomeres from totipotency to pluripotency, thereby affecting embryonic lineage differentiation. ZSA is an essential post-transcriptional process of MZT and has physiological significance in generating new life. In addition to transcriptional activation, appropriate expression of transcript isoforms is also necessary for preimplantation embryonic development.

Keywords: RNA processing; alternative splicing; early embryo; splicing factors; totipotency and pluripotency; zygotic genome activation.

MeSH terms

  • Animals
  • Embryonic Development / genetics
  • Humans
  • Mice
  • Nuclear Proteins / genetics
  • Poly(A)-Binding Proteins / genetics
  • Poly(A)-Binding Proteins / metabolism
  • Protein Isoforms / genetics
  • RNA Splicing
  • Transcriptome* / genetics
  • Zygote* / metabolism

Substances

  • Protein Isoforms
  • PABPN1L protein, human
  • Poly(A)-Binding Proteins
  • Dppa4 protein, mouse
  • Nuclear Proteins