CLAMP and Zelda function together to promote Drosophila zygotic genome activation

Author:

Duan Jingyue1ORCID,Rieder Leila2,Colonnetta Megan M3ORCID,Huang Annie1,Mckenney Mary1,Watters Scott4,Deshpande Girish13,Jordan William1,Fawzi Nicolas4,Larschan Erica1ORCID

Affiliation:

1. Department of Molecular Biology, Cellular Biology, and Biochemistry, Brown University, Providence, United States

2. Department of Biology, Emory University, Atlanta, United States

3. Department of Molecular Biology, Princeton University, Princeton, United States

4. Department of Molecular Pharmacology, Physiology and Biotechnology, Brown University, Providence, United States

Abstract

During the essential and conserved process of zygotic genome activation (ZGA), chromatin accessibility must increase to promote transcription. Drosophila is a well-established model for defining mechanisms that drive ZGA. Zelda (ZLD) is a key pioneer transcription factor (TF) that promotes ZGA in the Drosophila embryo. However, many genomic loci that contain GA-rich motifs become accessible during ZGA independent of ZLD. Therefore, we hypothesized that other early TFs that function with ZLD have not yet been identified, especially those that are capable of binding to GA-rich motifs such as chromatin-linked adaptor for male-specific lethal (MSL) proteins (CLAMP). Here, we demonstrate that Drosophila embryonic development requires maternal CLAMP to (1) activate zygotic transcription; (2) increase chromatin accessibility at promoters of specific genes that often encode other essential TFs; and (3) enhance chromatin accessibility and facilitate ZLD occupancy at a subset of key embryonic promoters. Thus, CLAMP functions as a pioneer factor that plays a targeted yet essential role in ZGA.

Funder

National Institute of General Medical Sciences

National Science Foundation

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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