ZNF16 is a nucleolar-associated protein that regulates expression of rDNA and cancer-associated genes
ZNF16 (also known as HZF1 and KOX9) is a multi-C2H2 zinc finger protein first identified via its expression in human T-cells and shown to have a role in blood cell differentiation. ZNF16 was later shown to be ubiquitously expressed in a variety of fetal and adult tissues, suggesting a broader function. In this study, we confirm the ubiquitous expression of ZNF16 in a variety of cancer and non-cancer cell lines and show that ZNF16 depletion reduces cell viability in all cell lines tested. Furthermore, we show that ZNF16 localizes to the nucleolus in a transcription-dependent manner, interacts with the intergenic spacer region of the rDNA and promotes rDNA transcription. Additionally, RNA-sequencing experiments after ZNF16 depletion revealed that ZNF16 also has roles in a variety of pathways including extracellular matrix-receptor interaction, focal adhesions, cytokine-cytokine receptor interactions, human papillomavirus infection and cancer pathways. These findings are consistent with broader roles for ZNF16, including the regulation of nucleolar function, a process that is essential for all cells, and provide evidence at the cellular/molecular level of its role in the regulation of cancer-associated genes (e.g. NRAS, BIRC3, EGFR).
Authors
- Nathan S. Reyna (ORCID: https://orcid.org/0000-0003-3430-0282)
- Arlene Levario
- Yasir Rahmatallah (ORCID: https://orcid.org/0000-0002-8176-6328)
- Jason Paratore
- Laura Quevedo (ORCID: https://orcid.org/0000-0001-8902-5818)
- Galina Glazko (ORCID: https://orcid.org/0000-0002-0570-5304)
- Chelsea L. George
- Laura Diaz-Martinez
- Matthew J. Alcaraz
Institutions
- Gonzaga University (US)
- The University of Texas at El Paso (US)
- Ouachita Baptist University (US)
- University of Arkansas for Medical Sciences (US)
Publication Details
- Journal
- Biology Open
- Published
- 2025-12-30
- DOI
- https://doi.org/10.1242/bio.062336
- Primary Topic
- Genetic Syndromes and Imprinting
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Science Foundation
- M.J. Murdock Charitable Trust
- National Institutes of Health
- National Institute of General Medical Sciences