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Rizzo, F.* ; Ben-Shem, A.* ; Timmers, H.T.M.* ; Bartke, T. ; Vincent, S.D.* ; Tora, L.*

Step-brothers in arms, SAGA and ATAC co-activator complexes, use different strategies.

EMBO J., DOI: 10.1038/s44318-026-00892-z (2026)
Verlagsversion Forschungsdaten DOI PMC
Open Access Gold
Creative Commons Lizenzvertrag
Transcriptional co-activator complexes play essential roles in regulating gene transcription by integrating signals from transcription factors and chromatin. Among these, the SAGA (Spt-Ada-Gcn5 acetyltransferase) and ATAC (Ada Two-A Containing) complexes represent related histone acetyltransferase assemblies that contain both shared and specific subunits. SAGA and ATAC possess similar and divergent enzymatic activities that shape their contributions to transcriptional control. Here, we review emerging evidence that highlights differential interactions of transcriptional activators with SAGA or ATAC and their differential chromatin-reading capabilities through specific recognition of histone modifications. Distinct requirements for SAGA and for ATAC have been observed in gene regulation important for maintaining cellular homeostasis and for oncogenic transformation, indicating that dysregulation of these complexes can contribute to cancer progression. The development of small-molecule inhibitors targeting key components of SAGA and/or ATAC offers promising strategies to disrupt their recruitment and transcriptional activity in cancer cells. Our review dissects the unique and overlapping functions of SAGA and ATAC, which are crucial for understanding regulation by these complexes in order to exploit them as targets in precision oncology.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Review
Schlagwörter Histone Acetyltransferase Complex; Chromatin-modifying Complex; Drosophila Ada2 Homologs; Human Staga Complex; Transcription Factor; H2b Ubiquitylation; Binding Protein; Activation Domain; Structural Basis; Gene-expression
ISSN (print) / ISBN 0261-4189
e-ISSN 1460-2075
Zeitschrift EMBO Journal, The
Verlag Springer
Verlagsort Heidelberg, Germany
Begutachtungsstatus Peer reviewed
Institut(e) Institiute of Functional Epigenetics (IFE)
Förderungen HHS | NIH | National Institute of General Medical Sciences (NIGMS)
Agence Nationale de la Recherche (ANR)
Deutsche Forschungsgemeinschaft (DFG)