Literature DB >> 27417138

Catalytically Active Proteasomes Function Predominantly in the Cytosol.

Francis Wang Dang1, Li Chen1, Kiran Madura2.   

Abstract

The ubiquitin/proteasome pathway is a well characterized system for degrading intracellular proteins, although many aspects remain poorly understood. There is, for instance, a conspicuous lack of understanding of the site(s) where nuclear proteins are degraded because the subcellular distribution of peptidase activity has not been investigated systematically. Although nuclear proteins could be degraded by importing proteasomes into the nucleus, it is also evident that some nuclear proteins are degraded only after export to cytosolic proteasomes. Proteasomes and substrates are mobile, and consequently, the sites of degradation might not be static. We sought to identify the location of proteasomes to provide more conclusive evidence on the sites of protein degradation. We report that catalytically active proteasomes exist almost exclusively in the cytosol. The resulting lack of nuclear peptidase activity suggests that little, if any, degradation occurs in the nucleus. These and other studies suggest that the export of proteolytic substrates could define an important regulatory step in the degradation of nuclear proteins by cytosolic proteasomes.
© 2016 by The American Society for Biochemistry and Molecular Biology, Inc.

Keywords:  E3 ubiquitin ligase; nuclear envelope; nuclear pore; proteasome; protein degradation; protein export; proteolysis

Mesh:

Substances:

Year:  2016        PMID: 27417138      PMCID: PMC5009251          DOI: 10.1074/jbc.M115.712406

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  52 in total

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4.  Sts1 plays a key role in targeting proteasomes to the nucleus.

Authors:  Li Chen; Lizbeth Romero; Show-Mei Chuang; Vincent Tournier; Kishore Kumar Joshi; Jung Ah Lee; Gopala Kovvali; Kiran Madura
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5.  The DNA damage-inducible UbL-UbA protein Ddi1 participates in Mec1-mediated degradation of Ho endonuclease.

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6.  Subcellular distribution of proteasomes implicates a major location of protein degradation in the nuclear envelope-ER network in yeast.

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7.  Chromatin-bound nuclear pore components regulate gene expression in higher eukaryotes.

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10.  Proteasome assembly influences interaction with ubiquitinated proteins and shuttle factors.

Authors:  Abhishek Chandra; Li Chen; Huiyan Liang; Kiran Madura
Journal:  J Biol Chem       Date:  2010-01-08       Impact factor: 5.157

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2.  Programmed cell death 4 mechanism of action: The model to be updated?

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3.  The Proline/Arginine Dipeptide from Hexanucleotide Repeat Expanded C9ORF72 Inhibits the Proteasome.

Authors:  Rahul Gupta; Matthews Lan; Jelena Mojsilovic-Petrovic; Won Hoon Choi; Nathaniel Safren; Sami Barmada; Min Jae Lee; Robert Kalb
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Authors:  Sahradha Albert; Miroslava Schaffer; Florian Beck; Shyamal Mosalaganti; Shoh Asano; Henry F Thomas; Jürgen M Plitzko; Martin Beck; Wolfgang Baumeister; Benjamin D Engel
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6.  Comprehensive Analysis of Proteasomal Complexes in Mouse Brain Regions Detects ENO2 as a Potential Partner of the Proteasome in the Striatum.

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Review 7.  Sledgehammer to Scalpel: Broad Challenges to the Heart and Other Tissues Yield Specific Cellular Responses via Transcriptional Regulation of the ER-Stress Master Regulator ATF6α.

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9.  MDM2-Driven Ubiquitination Rapidly Removes p53 from Its Cognate Promoters.

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Review 10.  Ubiquitin Ligase Redundancy and Nuclear-Cytoplasmic Localization in Yeast Protein Quality Control.

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