Caspase-dependent cleavage of nucleic acids

• Published in: Cell death and differentiation Vol. 7; no. 7; pp. 616 - 627
• Main Authors: Degen, W G, Pruijn, G J, Raats, J M, van Venrooij, W J
• Format: Journal Article
• Language: English
• Published: England Nature Publishing Group 01-07-2000
• Subjects: 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; Netherlands
• ISSN: 1350-9047; 1476-5403
• DOI: 10.1038/sj.cdd.4400672

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.