PUBLICATION
A cell cycle-coordinated Polymerase II transcription compartment encompasses gene expression before global genome activation
- Authors
- Hadzhiev, Y., Qureshi, H.K., Wheatley, L., Cooper, L., Jasiulewicz, A., Van Nguyen, H., Wragg, J.W., Poovathumkadavil, D., Conic, S., Bajan, S., Sik, A., Hutvàgner, G., Tora, L., Gambus, A., Fossey, J.S., Müller, F.
- ID
- ZDB-PUB-190212-4
- Date
- 2019
- Source
- Nature communications 10: 691 (Journal)
- Registered Authors
- Hadzhiev, Yavor, Müller, Ferenc
- Keywords
- none
- MeSH Terms
-
- Blastula/diagnostic imaging
- Blastula/physiology
- Cell Cycle/genetics*
- Cell Cycle/physiology
- Blastocyst/physiology
- PubMed
- 30741925 Full text @ Nat. Commun.
Abstract
Most metazoan embryos commence development with rapid, transcriptionally silent cell divisions, with genome activation delayed until the mid-blastula transition (MBT). However, a set of genes escapes global repression and gets activated before MBT. Here we describe the formation and the spatio-temporal dynamics of a pair of distinct transcription compartments, which encompasses the earliest gene expression in zebrafish. 4D imaging of pri-miR430 and zinc-finger-gene activities by a novel, native transcription imaging approach reveals transcriptional sharing of nuclear compartments, which are regulated by homologous chromosome organisation. These compartments carry the majority of nascent-RNAs and active Polymerase II, are chromatin-depleted and represent the main sites of detectable transcription before MBT. Transcription occurs during the S-phase of increasingly permissive cleavage cycles. It is proposed, that the transcription compartment is part of the regulatory architecture of embryonic nuclei and offers a transcriptionally competent environment to facilitate early escape from repression before global genome activation.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping