Maternal TDP-43 interacts with RNA Pol II and regulates zygotic genome activation

Nat Commun. 2023 Jul 17;14(1):4275. doi: 10.1038/s41467-023-39924-1.

Abstract

Zygotic genome activation (ZGA) is essential for early embryonic development. However, the regulation of ZGA remains elusive in mammals. Here we report that a maternal factor TDP-43, a nuclear transactive response DNA-binding protein, regulates ZGA through RNA Pol II and is essential for mouse early embryogenesis. Maternal TDP-43 translocates from the cytoplasm into the nucleus at the early two-cell stage when minor to major ZGA transition occurs. Genetic deletion of maternal TDP-43 results in mouse early embryos arrested at the two-cell stage. TDP-43 co-occupies with RNA Pol II as large foci in the nucleus and also at the promoters of ZGA genes at the late two-cell stage. Biochemical evidence indicates that TDP-43 binds Polr2a and Cyclin T1. Depletion of maternal TDP-43 caused the loss of Pol II foci and reduced Pol II binding on chromatin at major ZGA genes, accompanied by defective ZGA. Collectively, our results suggest that maternal TDP-43 is critical for mouse early embryonic development, in part through facilitating the correct RNA Pol II configuration and zygotic genome activation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Embryonic Development / genetics
  • Gene Expression Regulation, Developmental*
  • Mammals / genetics
  • Mice
  • RNA Polymerase II* / genetics
  • RNA Polymerase II* / metabolism
  • Zygote / metabolism

Substances

  • RNA Polymerase II
  • DNA-Binding Proteins
  • TDP-43 protein, mouse