The Drosophila Dbf4 ortholog Chiffon forms a complex with Gcn5 that is necessary for histone acetylation and viability

Author:

Torres-Zelada Eliana F.1ORCID,Stephenson Robert E.1,Alpsoy Aktan2,Anderson Benjamin D.1,Swanson Selene K.3,Florens Laurence3,Dykhuizen Emily C.2ORCID,Washburn Michael P.34,Weake Vikki M.15ORCID

Affiliation:

1. Department of Biochemistry, Purdue University, West Lafayette, Indiana 47907, USA

2. Department of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, Indiana 47907, USA

3. Stowers Institute for Medical Research, 1000 E. 50th St., Kansas City, Missouri 64110, USA

4. Department of Pathology and Laboratory Medicine, University of Kansas Medical Center, 3901 Rainbow Boulevard, Kansas City, Kansas 66160, USA

5. Purdue University Center for Cancer Research, Purdue University, West Lafayette, Indiana 47907, USA

Abstract

Metazoans contain two homologs of the Gcn5-binding protein Ada2, Ada2a and Ada2b, which nucleate formation of the ATAC and SAGA complexes respectively. In Drosophila melanogaster, there are two splice isoforms of Ada2b: Ada2b-PA and Ada2b-PB. Here we show only the Ada2b-PB isoform is in SAGA; in contrast, Ada2b-PA associates with Gcn5, Ada3, Sgf29 and Chiffon forming the Chiffon Histone Acetyltransferase (CHAT) complex. Chiffon is the Drosophila ortholog of Dbf4, which binds and activates the cell cycle kinase Cdc7 to initiate DNA replication. In flies, Chiffon and Cdc7 are required in ovary follicle cells for gene amplification, a specialized form of DNA re-replication. Although chiffon was previously reported to be dispensable for viability, here we find that Chiffon is required for both histone acetylation and viability in flies. Surprisingly, we show that chiffon is a dicistronic gene that encodes distinct Cdc7- and CHAT-binding polypeptides. Although the Cdc7-binding domain of Chiffon is not required for viability in flies, Chiffon's CHAT-binding domain is essential for viability but is not required for gene amplification, arguing against a role in DNA replication.

Funder

National Institute of General Medical Sciences

Publisher

The Company of Biologists

Subject

Cell Biology

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