4.7 Article

Histone concentration regulates the cell cycle and transcription in early development

Journal

DEVELOPMENT
Volume 146, Issue 19, Pages -

Publisher

COMPANY BIOLOGISTS LTD
DOI: 10.1242/dev.177402

Keywords

Chromatin; Maternal to zygotic transition; MZT; Mid-blastula transition; MBT; Zygotic genome activation; ZGA; Nuclear cytoplasmic ratio; Cell cycle

Funding

  1. Lewis-Sigler Fellows program at Princeton University, USA

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The early embryos of many animals, including flies, fish and frogs, have unusually rapid cell cycles and delayed onset of transcription. These divisions are dependent on maternally supplied RNAs and proteins including histones. Previous work suggests that the pool size of maternally provided histones can alter the timing of zygotic genome activation (ZGA) in frogs and fish. Here, we examine the effects of under- and overexpression of maternal histones in Drosophila embryogenesis. Decreasing histone concentration advances zygotic transcription, cell cycle elongation, Chk1 activation and gastrulation. Conversely, increasing histone concentration delays transcription and results in an additional nuclear cycle before gastrulation. Numerous zygotic transcripts are sensitive to histone concentration, and the promoters of histone-sensitive genes are associated with specific chromatin features linked to increased histone turnover. These include enrichment of the pioneer transcription factor Zelda, and lack of SIN3A and associated histone deacetylases. Our findings uncover a crucial regulatory role for histone concentrations in ZGA of Drosophila.

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