Nucleoli and the nucleoli–centromere association are dynamic during normal development and in cancer

Aaron Rodrigues, Kyle L. MacQuarrie, Emma Freeman, Alicia Lin, Alexander B. Willis, Zhaofa Xu, Angel A. Alvarez, Yongchao Ma, Bethany E. Perez White, Daniel R. Foltz, Sui Huang*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

Centromeres are known to cluster around nucleoli in Drosophila and mammalian cells, but the significance of the nucleoli–centromere interaction remains underexplored. To determine whether the interaction is dynamic under different physiological and pathological conditions, we examined nucleolar structure and centromeres at various differentiation stages using cell culture models and the results showed dynamic changes in nucleolar characteristics and nucleoli–centromere interactions through differentiation and in cancer cells. Embryonic stem cells usually have a single large nucleolus, which is clustered with a high percentage of centromeres. As cells differentiate into intermediate states, the nucleolar number increases and the centromere association decreases. In terminally differentiated cells, including myotubes, neurons, and keratinocytes, the number of nucleoli and their association with centromeres are at the lowest. Cancer cells demonstrate the pattern of nucleoli number and nucleoli–centromere association that is akin to proliferative cell types, suggesting that nucleolar reorganization and changes in nucleoli–centromere interactions may play a role in facilitating malignant transformation. This idea is supported in a case of pediatric rhabdomyosarcoma, in which induced differentiation reduces the nucleolar number and centromere association. These findings suggest active roles of nucleolar structure in centromere function and genome organization critical for cellular function in both normal development and cancer.

Original languageEnglish (US)
Article numberbr5
JournalMolecular biology of the cell
Volume34
Issue number4
DOIs
StatePublished - Apr 2023

Funding

D.R.F. is funded by GM1111907 and U10CA260699. Y.C.M. was supported by NIH R01NS-094564 and R21NS-106307. B.E.P.W. was supported by NIH NIAMS Grants no. K01AR-072773 and no. P30AR-075049. S.H. was supported by U10CA260699. K.L.M. is supported, in part, by the NIH’s National Center for Advancing Translational Sciences, Grant no. KL2TR-001424, as well as the Hyundai Hope on Wheels Scholar Hope Grant, the Stanley Manne Children’s Research Institute, and the Ann & Robert H. Lurie Children’s Hospital of Chicago. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH. We would also like to thank Robert Goldman for the CREST and lamin A antibodies, Thomas Meier for Nopp140 antibodies, and Joe Ibarra for technical assistance as well as Steven Kosak and Kurt Leano. We would also like to thank Stephen Adam, Paul Kaufman, and Anastassiia Vertii for critical reading.

ASJC Scopus subject areas

  • Molecular Biology
  • Cell Biology

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