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The human exosome: an autoantigenic complex of exoribonucleases in myositis and scleroderma

The anti-PM/Scl autoantibodies are known to characterize a subset of autoimmune patients with myositis, scleroderma (Scl), and the PM/Scl overlap syndrome. The major autoantigens that are recognized by anti-PM/Scl autoantibodies are designated PM/Scl-100 and PM/Scl-75. These autoantigens have been r...

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Autores principales: Brouwer, Rick, Pruijn, Ger JM, van Venrooij, Walther J
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC128886/
https://www.ncbi.nlm.nih.gov/pubmed/11178117
http://dx.doi.org/10.1186/ar147
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author Brouwer, Rick
Pruijn, Ger JM
van Venrooij, Walther J
author_facet Brouwer, Rick
Pruijn, Ger JM
van Venrooij, Walther J
author_sort Brouwer, Rick
collection PubMed
description The anti-PM/Scl autoantibodies are known to characterize a subset of autoimmune patients with myositis, scleroderma (Scl), and the PM/Scl overlap syndrome. The major autoantigens that are recognized by anti-PM/Scl autoantibodies are designated PM/Scl-100 and PM/Scl-75. These autoantigens have been reported to associate into a large complex consisting of 11 to 16 proteins and to play a role in ribosome synthesis. Recently, it was discovered that the PM/Scl complex is the human counterpart of the yeast (Saccharomyces cerevisiae) exosome, which is an RNA-processing complex consisting of 11 3' → 5' exoribonucleases. To date, 10 human exosome components have been identified, although only some of these were studied in more detail. In this review, we discuss some recent advances in the characterization of the PM/Scl complex.
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spelling pubmed-1288862002-10-28 The human exosome: an autoantigenic complex of exoribonucleases in myositis and scleroderma Brouwer, Rick Pruijn, Ger JM van Venrooij, Walther J Arthritis Res Review The anti-PM/Scl autoantibodies are known to characterize a subset of autoimmune patients with myositis, scleroderma (Scl), and the PM/Scl overlap syndrome. The major autoantigens that are recognized by anti-PM/Scl autoantibodies are designated PM/Scl-100 and PM/Scl-75. These autoantigens have been reported to associate into a large complex consisting of 11 to 16 proteins and to play a role in ribosome synthesis. Recently, it was discovered that the PM/Scl complex is the human counterpart of the yeast (Saccharomyces cerevisiae) exosome, which is an RNA-processing complex consisting of 11 3' → 5' exoribonucleases. To date, 10 human exosome components have been identified, although only some of these were studied in more detail. In this review, we discuss some recent advances in the characterization of the PM/Scl complex. BioMed Central 2001 2000-12-20 /pmc/articles/PMC128886/ /pubmed/11178117 http://dx.doi.org/10.1186/ar147 Text en Copyright © 2001 BioMed Central Ltd on behalf of the copyright holder
spellingShingle Review
Brouwer, Rick
Pruijn, Ger JM
van Venrooij, Walther J
The human exosome: an autoantigenic complex of exoribonucleases in myositis and scleroderma
title The human exosome: an autoantigenic complex of exoribonucleases in myositis and scleroderma
title_full The human exosome: an autoantigenic complex of exoribonucleases in myositis and scleroderma
title_fullStr The human exosome: an autoantigenic complex of exoribonucleases in myositis and scleroderma
title_full_unstemmed The human exosome: an autoantigenic complex of exoribonucleases in myositis and scleroderma
title_short The human exosome: an autoantigenic complex of exoribonucleases in myositis and scleroderma
title_sort human exosome: an autoantigenic complex of exoribonucleases in myositis and scleroderma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC128886/
https://www.ncbi.nlm.nih.gov/pubmed/11178117
http://dx.doi.org/10.1186/ar147
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