Coordinating transcription and replication to mitigate their conflicts in early Drosophila embryos

Cell Rep. 2022 Oct 18;41(3):111507. doi: 10.1016/j.celrep.2022.111507.

Abstract

Collisions between transcribing RNA polymerases and DNA replication forks are disruptive. The threat of collisions is particularly acute during the rapid early embryonic cell cycles of Drosophila when S phase occupies the entirety of interphase. We hypothesize that collision-avoidance mechanisms safeguard this early transcription. Real-time imaging of endogenously tagged RNA polymerase II (RNAPII) and a reporter for nascent transcripts in unperturbed embryos shows clustering of RNAPII at around 2 min after mitotic exit, followed by progressive dispersal as associated nascent transcripts accumulate later in interphase. Abrupt inhibition of various steps in DNA replication, including origin licensing, origin firing, and polymerization, suppresses post-mitotic RNAPII clustering and transcription in nuclear cycles. We propose that replication dependency defers the onset of transcription so that RNAPII transcribes behind advancing replication forks. The resulting orderly progression can explain how early embryos circumvent transcription-replication conflicts to express essential developmental genes.

Keywords: CP: Developmental biology; CP: Molecular biology; Drosophila; RNA polymerase II; embryonic cell cycle; live imaging; transcription-replication conflict; zygotic transcription.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • DNA-Directed RNA Polymerases / metabolism
  • Drosophila Proteins* / genetics
  • Drosophila Proteins* / metabolism
  • Drosophila* / metabolism
  • RNA Polymerase II / metabolism
  • S Phase

Substances

  • RNA Polymerase II
  • Drosophila Proteins
  • DNA-Directed RNA Polymerases