A cell cycle-coordinated Polymerase II transcription compartment encompasses gene expression before global genome activation

Yavor Hadzhiev(University of Birmingham), Haseeb K. Qureshi(University of Birmingham), Lucy Wheatley(University of Birmingham), Ledean Cooper(University of Birmingham), Aleksandra Jasiulewicz(University of Birmingham), Huy V. Nguyen(University of Birmingham), Joseph W. Wragg(University of Birmingham), Divyasree Poovathumkadavil(University of Birmingham), Sascha Conic(Institut de génétique et de biologie moléculaire et cellulaire), Sarah Bajan(University of Technology Sydney), Attila Sı́k(University of Birmingham), György Hutvágner(University of Technology Sydney), Làszlò Tora(Institut de génétique et de biologie moléculaire et cellulaire), Agnieszka Gambus(University of Birmingham), John Fossey(University of Birmingham), Ferenc Müller(University of Birmingham)
Nature Communications
February 11, 2019
Cited by 260Open Access
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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.


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