Cellular maintenance of nuclear protein homeostasis
Cellular maintenance of nuclear protein homeostasis
The accumulation and aggregation of misfolded proteins is the primary hallmark for more than 45 human degenerative diseases. These devastating disorders include Alzheimer's, Parkinson's, Huntington's, and amyotrophic lateral sclerosis. Over 15 degenerative diseases are associated with the aggregation of misfolded proteins specifically in the nucleus of cells. However, how the cell safeguards the nucleus from misfolded proteins is not entirely clear. In this review, we discuss what is currently known about the cellular mechanisms that maintain protein homeostasis in the nucleus and protect the nucleus from misfolded protein accumulation and aggregation. In particular, we focus on the chaperones found to localize to the nucleus during stress, the ubiquitin-proteasome components enriched in the nucleus, the signaling systems that might be present in the nucleus to coordinate folding and degradation, and the sites of misfolded protein deposition associated with the nucleus.
Cell Nucleus/metabolism, Homeostasis, Humans, Molecular Chaperones/metabolism, Nuclear Proteins/chemistry, Proteasome Endopeptidase Complex/metabolism, Signal Transduction, Sumoylation, Ubiquitin/metabolism, Ubiquitin-Protein Ligases/chemistry
1865-79
Gallagher, Pamela S
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Oeser, Michelle L
3fe66ab8-6a12-442b-b21b-82116ca2b456
Abraham, Ayelet-chen
9d7bdc49-a883-463d-acce-8635fa88e8b1
Kaganovich, Daniel
ebb13f4e-e925-4aef-88e7-ddc25ef52d8f
Gardner, Richard G
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1 May 2014
Gallagher, Pamela S
a4f5d773-f2ec-4e01-aa9e-e8e4300dba4b
Oeser, Michelle L
3fe66ab8-6a12-442b-b21b-82116ca2b456
Abraham, Ayelet-chen
9d7bdc49-a883-463d-acce-8635fa88e8b1
Kaganovich, Daniel
ebb13f4e-e925-4aef-88e7-ddc25ef52d8f
Gardner, Richard G
0e858b70-0e70-4b2b-9080-0389b6a4f6e4
Gallagher, Pamela S, Oeser, Michelle L, Abraham, Ayelet-chen, Kaganovich, Daniel and Gardner, Richard G
(2014)
Cellular maintenance of nuclear protein homeostasis.
Cellular and Molecular Life Sciences, 71 (10), .
(doi:10.1007/s00018-013-1530-y).
Abstract
The accumulation and aggregation of misfolded proteins is the primary hallmark for more than 45 human degenerative diseases. These devastating disorders include Alzheimer's, Parkinson's, Huntington's, and amyotrophic lateral sclerosis. Over 15 degenerative diseases are associated with the aggregation of misfolded proteins specifically in the nucleus of cells. However, how the cell safeguards the nucleus from misfolded proteins is not entirely clear. In this review, we discuss what is currently known about the cellular mechanisms that maintain protein homeostasis in the nucleus and protect the nucleus from misfolded protein accumulation and aggregation. In particular, we focus on the chaperones found to localize to the nucleus during stress, the ubiquitin-proteasome components enriched in the nucleus, the signaling systems that might be present in the nucleus to coordinate folding and degradation, and the sites of misfolded protein deposition associated with the nucleus.
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More information
Accepted/In Press date: 19 November 2013
Published date: 1 May 2014
Keywords:
Cell Nucleus/metabolism, Homeostasis, Humans, Molecular Chaperones/metabolism, Nuclear Proteins/chemistry, Proteasome Endopeptidase Complex/metabolism, Signal Transduction, Sumoylation, Ubiquitin/metabolism, Ubiquitin-Protein Ligases/chemistry
Identifiers
Local EPrints ID: 474161
URI: http://eprints.soton.ac.uk/id/eprint/474161
ISSN: 1420-682X
PURE UUID: fcf22f5f-9f38-479e-ab90-5276c322fc88
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Date deposited: 14 Feb 2023 17:49
Last modified: 17 Mar 2024 04:17
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Contributors
Author:
Pamela S Gallagher
Author:
Michelle L Oeser
Author:
Ayelet-chen Abraham
Author:
Daniel Kaganovich
Author:
Richard G Gardner
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