Abstract
Annual Review of Immunology
Vol. 23:
853-875
(Volume publication date April 2005)
(doi:10.1146/annurev.immunol.23.021704.115811)
First published online as a Review in Advance on December 17, 2004DNA DEGRADATION IN DEVELOPMENT AND PROGRAMMED CELL DEATH Shigekazu NagataLaboratory of Genetics, Integrated Biology Laboratories, Graduate School of Frontier Biosciences, Osaka University; Department of Genetics, Osaka University Medical School; Solution Oriented Research for Science and Technology, Japanese Science and Technology Agency, Osaka, Japan; email: nagata@genetic.med.osaka-u.ac.jp ▪ Abstract Most mammalian cells have nuclei that contain DNA, which replicates during cell proliferation. DNA is destroyed by various developmental processes in mammals. It is degraded during programmed cell death that accompanies mammalian development. The nuclei of erythrocytes and eye lens fiber cells are also removed during their differentiation into mature cells. If DNA is not properly degraded in these processes, it can cause various diseases, including tissue atrophy, anemia, cataract, and autoimmune diseases, which indicates that DNA can be a pathogenic molecule. Here, I present how DNA is degraded during programmed cell death, erythroid cell differentiation, and lens cell differentiation. I discuss what might be or will be learned from understanding the molecular mechanisms of DNA degradation that occurs during mammalian development. Most recent citing papers (via CrossRef)Cell-autonomous requirement for DNaseII in nonapoptotic cell death Cell Death and Differentiation (2009) Aeromonas Spp. Human Isolates Induce Apoptosis of Murine Macrophages Current Microbiology 58(3):252-257 (2009) IFN regulatory factor (IRF) 3/7-dependent and -independent gene induction by mammalian DNA that escapes degradation European Journal of Immunology 38(11):3150-3158 (2008) Hypothetical review: thymic aberrations and type-I interferons; attempts to deduce autoimmunizing mechanisms from unexpected clues in monogenic and paraneoplastic syndromes Clinical & Experimental Immunology 154(1):141-151 (2008) Mechanism of DNA Fragmentation During Hypoxia in the Cerebral Cortex of Newborn Piglets Neurochemical Research 33(7):1232-1237 (2008)
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