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ZNF16 is a nucleolar-associated protein that regulates expression of rDNA and cancer-associated genes

  • Chelsea L. George
    ,
  • Laura A. Espinoza Quevedo
    ,
  • Jason Paratore
    ,
  • Matthew J. Alcaraz
    ,
  • Arlene P. Levario
    ,
  • Yasir Rahmatallah
*Corresponding author for this work
  • University of Texas at El Paso
    ,
  • University of Arkansas for Medical Sciences
    ,
  • Ouachita Baptist University
    ,
Research Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

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).

Bibliographic Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Journal (Volume, Issue Number)

Biology Open (Volume 15, Issue 1)

Publication milestones

  • Published - 01/2026

Publication status

Published - 01/2026

Publication IDs

  • Scopus: 105032260630
  • PubMed: 41467516