Myosin VI in the nucleolus of neurosecretory PC12 cells: its involvement in the maintenance of nucleolar structure and ribosome organization.

B23 PC12 cells actinomycin D fibrillarin myosin VI nucleolar stress nucleolin nucleolus

Journal

Frontiers in physiology
ISSN: 1664-042X
Titre abrégé: Front Physiol
Pays: Switzerland
ID NLM: 101549006

Informations de publication

Date de publication:
2024
Historique:
received: 10 01 2024
accepted: 01 04 2024
medline: 22 5 2024
pubmed: 22 5 2024
entrez: 22 5 2024
Statut: epublish

Résumé

We have previously shown that unconventional myosin VI (MVI), a unique actin-based motor protein, shuttles between the cytoplasm and nucleus in neurosecretory PC12 cells in a stimulation-dependent manner and interacts with numerous proteins involved in nuclear processes. Among the identified potential MVI partners was nucleolin, a major nucleolar protein implicated in rRNA processing and ribosome assembly. Several other nucleolar proteins such as fibrillarin, UBF (upstream binding factor), and B23 (also termed nucleophosmin) have been shown to interact with MVI. A bioinformatics tool predicted the presence of the nucleolar localization signal (NoLS) within the MVI globular tail domain, and immunostaining confirmed the presence of MVI within the nucleolus. Depletion of MVI, previously shown to impair PC12 cell proliferation and motility, caused disorganization of the nucleolus and rough endoplasmic reticulum (rER). However, lack of MVI does not affect nucleolar transcription. In light of these data, we propose that MVI is important for nucleolar and ribosome maintenance but not for RNA polymerase 1-related transcription.

Identifiants

pubmed: 38774650
doi: 10.3389/fphys.2024.1368416
pii: 1368416
pmc: PMC11106421
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1368416

Informations de copyright

Copyright © 2024 Nowak, Lenartowski, Kalita, Lehka, Karatsai, Lenartowska and Rędowicz.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.

Auteurs

Jolanta Nowak (J)

Laboratory of Molecular Basis of Cell Motility, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland.

Robert Lenartowski (R)

Faculty of Biological and Veterinary Sciences, Nicolaus Copernicus University in Torun, Torun, Poland.
Centre for Modern Interdisciplinary Technologies, Nicolaus Copernicus University in Torun, Torun, Poland.

Katarzyna Kalita (K)

Laboratory of Neurobiology, Nencki-EMBL Partnership for Neural Plasticity and Brain Disorders-BRAINCITY, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland.

Lilya Lehka (L)

Laboratory of Molecular Basis of Cell Motility, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland.

Olena Karatsai (O)

Laboratory of Molecular Basis of Cell Motility, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland.

Marta Lenartowska (M)

Faculty of Biological and Veterinary Sciences, Nicolaus Copernicus University in Torun, Torun, Poland.
Centre for Modern Interdisciplinary Technologies, Nicolaus Copernicus University in Torun, Torun, Poland.

Maria Jolanta Rędowicz (MJ)

Laboratory of Molecular Basis of Cell Motility, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland.

Classifications MeSH