Cell cycle-dependent localization of the proteasome to chromatin.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
02 04 2020
Historique:
received: 14 11 2019
accepted: 12 03 2020
entrez: 4 4 2020
pubmed: 4 4 2020
medline: 25 11 2020
Statut: epublish

Résumé

An integrative understanding of nuclear events including transcription in normal and cancer cells requires comprehensive and quantitative measurement of protein dynamics that underlie such events. However, the low abundance of most nuclear proteins hampers their detailed functional characterization. We have now comprehensively quantified the abundance of nuclear proteins with the use of proteomics approaches in both normal and transformed human diploid fibroblasts. We found that subunits of the 26S proteasome complex were markedly down-regulated in the nuclear fraction of the transformed cells compared with that of the wild-type cells. The intranuclear proteasome abundance appeared to be inversely related to the rate of cell cycle progression, with restraint of the cell cycle being associated with an increase in the amount of proteasome subunits in the nucleus, suggesting that the nuclear proteasome content is dependent on the cell cycle. Furthermore, chromatin enrichment for proteomics (ChEP) analysis revealed enrichment of the proteasome in the chromatin fraction of quiescent cells and its apparent dissociation from chromatin in transformed cells. Our results thus suggest that translocation of the nuclear proteasome to chromatin may play an important role in control of the cell cycle and oncogenesis through regulation of chromatin-associated transcription factors.

Identifiants

pubmed: 32242037
doi: 10.1038/s41598-020-62697-2
pii: 10.1038/s41598-020-62697-2
pmc: PMC7118148
doi:

Substances chimiques

Chromatin 0
Proteome 0
Proteasome Endopeptidase Complex EC 3.4.25.1
ATP dependent 26S protease EC 3.4.99.-

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

5801

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Auteurs

Yuki Kito (Y)

Division of Cell Biology and Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.

Masaki Matsumoto (M)

Division of Proteomics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan. masakim@med.niigata-u.ac.jp.
Department of Omics and Systems Biology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan. masakim@med.niigata-u.ac.jp.

Atsushi Hatano (A)

YCI Laboratory for Trans-Omics, Young Chief Investigator Program, RIKEN Center for Integrative Medical Sciences, Kanagawa, Japan.

Tomoyo Takami (T)

Department of Omics and Systems Biology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.

Kiyotaka Oshikawa (K)

Department of Omics and Systems Biology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.

Akinobu Matsumoto (A)

Division of Cell Biology and Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.

Keiichi I Nakayama (KI)

Division of Cell Biology and Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan. nakayak1@bioreg.kyushu-u.ac.jp.
Division of Proteomics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan. nakayak1@bioreg.kyushu-u.ac.jp.

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