Caspase-dependent cleavage of nucleic acids
Autoimmune diseases are frequently characterized by the presence of autoantibodies directed against nucleic acid-protein complexes present in the nucleus of the cell. The mechanisms by which these autoantigenic molecules escape immunological tolerance are largely unknown, although a number of recent...
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Published in: | Cell death and differentiation Vol. 7; no. 7; pp. 616 - 627 |
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01-07-2000
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Abstract | Autoimmune diseases are frequently characterized by the presence of autoantibodies directed against nucleic acid-protein complexes present in the nucleus of the cell. The mechanisms by which these autoantigenic molecules escape immunological tolerance are largely unknown, although a number of recent observations suggest that modified self-proteins generated during apoptosis may play an important role in the development of autoimmunity. It has been hypothesized that the recognition of these modified self-proteins by the immune system may promote autoantibody production. While apoptosis is specifically characterized by posttranslational modification of proteins, recent findings also show that nucleic acids are modified. This review summarizes the specific cleavages of some of these key nucleic acids, i.e. chromosomal DNA, ribosomal RNA and small structural RNAs (U1 snRNA, Y RNA), in apoptotic cells. |
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AbstractList | Autoimmune diseases are frequently characterized by the presence of autoantibodies directed against nucleic acid-protein complexes present in the nucleus of the cell. The mechanisms by which these autoantigenic molecules escape immunological tolerance are largely unknown, although a number of recent observations suggest that modified self-proteins generated during apoptosis may play an important role in the development of autoimmunity. It has been hypothesized that the recognition of these modified self-proteins by the immune system may promote autoantibody production. While apoptosis is specifically characterized by posttranslational modification of proteins, recent findings also show that nucleic acids are modified. This review summarizes the specific cleavages of some of these key nucleic acids, i.e. chromosomal DNA, ribosomal RNA and small structural RNAs (U1 snRNA, Y RNA), in apoptotic cells. |
Author | Pruijn, G J Raats, J M Degen, W G van Venrooij, W J |
Author_xml | – sequence: 1 givenname: W G surname: Degen fullname: Degen, W G organization: Department of Biochemistry, University of Nijmegen, P.O. Box 9101, NL-6500 HB Nijmegen, The Netherlands – sequence: 2 givenname: G J surname: Pruijn fullname: Pruijn, G J – sequence: 3 givenname: J M surname: Raats fullname: Raats, J M – sequence: 4 givenname: W J surname: van Venrooij fullname: van Venrooij, W J |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/10889506$$D View this record in MEDLINE/PubMed |
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SubjectTerms | Animals Antigens Apoptosis Apoptosis - physiology Apoptosis Regulatory Proteins Autoantigens - genetics Autoantigens - immunology Autoantigens - metabolism Autoimmune diseases Autoimmune Diseases - immunology Autoimmune Diseases - metabolism Autoimmunity - genetics Autoimmunity - physiology Base Sequence Biochemistry Caspases - metabolism Cell death Deoxyribonucleases - metabolism DNA - metabolism DNA Fragmentation Humans Immune system Immunology Models, Molecular Molecular Sequence Data Proteins Ribonucleoproteins, Small Nuclear - immunology RNA - metabolism RNA, Ribosomal - immunology RNA, Ribosomal - metabolism snRNA U1 |
Title | Caspase-dependent cleavage of nucleic acids |
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