Native Chromatin Proteomics Reveals a Role for Specific Nucleoporins in Heterochromatin Organization and Maintenance.


Journal

Molecular cell
ISSN: 1097-4164
Titre abrégé: Mol Cell
Pays: United States
ID NLM: 9802571

Informations de publication

Date de publication:
02 01 2020
Historique:
received: 06 03 2019
revised: 19 08 2019
accepted: 11 10 2019
pubmed: 1 12 2019
medline: 28 3 2020
entrez: 1 12 2019
Statut: ppublish

Résumé

Spatially and functionally distinct domains of heterochromatin and euchromatin play important roles in the maintenance of chromosome stability and regulation of gene expression, but a comprehensive knowledge of their composition is lacking. Here, we develop a strategy for the isolation of native Schizosaccharomyces pombe heterochromatin and euchromatin fragments and analyze their composition by using quantitative mass spectrometry. The shared and euchromatin-specific proteomes contain proteins involved in DNA and chromatin metabolism and in transcription, respectively. The heterochromatin-specific proteome includes all proteins with known roles in heterochromatin formation and, in addition, is enriched for subsets of nucleoporins and inner nuclear membrane (INM) proteins, which associate with different chromatin domains. While the INM proteins are required for the integrity of the nucleolus, containing ribosomal DNA repeats, the nucleoporins are required for aggregation of heterochromatic foci and epigenetic inheritance. The results provide a comprehensive picture of heterochromatin-associated proteins and suggest a role for specific nucleoporins in heterochromatin function.

Identifiants

pubmed: 31784357
pii: S1097-2765(19)30796-8
doi: 10.1016/j.molcel.2019.10.018
pmc: PMC7224636
mid: NIHMS1547202
pii:
doi:

Substances chimiques

Chromatin 0
DNA, Ribosomal 0
Euchromatin 0
Heterochromatin 0
Nuclear Pore Complex Proteins 0
Schizosaccharomyces pombe Proteins 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

51-66.e8

Subventions

Organisme : NIGMS NIH HHS
ID : R01 GM072805
Pays : United States
Organisme : NCI NIH HHS
ID : P01 CA196539
Pays : United States
Organisme : NIDDK NIH HHS
ID : K01 DK098285
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM110174
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM132129
Pays : United States

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

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Auteurs

Nahid Iglesias (N)

Howard Hughes Medical Institute, Department of Cell Biology, Harvard Medical School, Boston, MA, USA.

Joao A Paulo (JA)

Department of Cell Biology, Harvard Medical School, Boston, MA, USA.

Antonis Tatarakis (A)

Howard Hughes Medical Institute, Department of Cell Biology, Harvard Medical School, Boston, MA, USA.

Xiaoyi Wang (X)

Howard Hughes Medical Institute, Department of Cell Biology, Harvard Medical School, Boston, MA, USA.

Amanda L Edwards (AL)

Massachusetts General Hospital Cancer Center and Department of Medicine, Harvard Medical School, Charlestown, MA, USA.

Natarajan V Bhanu (NV)

Department of Biochemistry and Biophysics, Epigenetics Program, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Benjamin A Garcia (BA)

Department of Biochemistry and Biophysics, Epigenetics Program, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Wilhelm Haas (W)

Department of Cell Biology, Harvard Medical School, Boston, MA, USA; Massachusetts General Hospital Cancer Center and Department of Medicine, Harvard Medical School, Charlestown, MA, USA.

Steven P Gygi (SP)

Department of Cell Biology, Harvard Medical School, Boston, MA, USA.

Danesh Moazed (D)

Howard Hughes Medical Institute, Department of Cell Biology, Harvard Medical School, Boston, MA, USA. Electronic address: danesh@hms.harvard.edu.

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Classifications MeSH