[HTML][HTML] Fate mapping for activation-induced cytidine deaminase (AID) marks non-lymphoid cells during mouse development

PC Rommel, D Bosque, AD Gitlin, GF Croft, N Heintz… - PLoS …, 2013 - journals.plos.org
PC Rommel, D Bosque, AD Gitlin, GF Croft, N Heintz, R Casellas, MC Nussenzweig
PLoS One, 2013journals.plos.org
The Aicda gene encodes Activation-Induced cytidine Deaminase (AID), an enzyme essential
for remodeling antibody genes in mature B lymphocytes. AID is also responsible for DNA
damage at oncogenes, leading to their mutation and cancer-associated chromosome
translocation in lymphoma. We used fate mapping and AIDGFP reporter mice to determine if
AID expression in the mouse extends beyond lymphocytes. We discovered that AIDcre tags
a small fraction of non-lymphoid cells starting at 10.5 days post conception (dpc), and that …
The Aicda gene encodes Activation-Induced cytidine Deaminase (AID), an enzyme essential for remodeling antibody genes in mature B lymphocytes. AID is also responsible for DNA damage at oncogenes, leading to their mutation and cancer-associated chromosome translocation in lymphoma. We used fate mapping and AIDGFP reporter mice to determine if AID expression in the mouse extends beyond lymphocytes. We discovered that AIDcre tags a small fraction of non-lymphoid cells starting at 10.5 days post conception (dpc), and that AIDGFP+ cells are detectable at dpc 11.5 and 12.5. Embryonic cells are tagged by AIDcre in the submandibular region, where conditional deletion of the tumor suppressor PTEN causes squamous papillomas. AIDcre also tags non-lymphoid cells in the embryonic central nervous system. Finally, in the adult mouse brain, AIDcre marks a small fraction of diverse neurons and distinct neuronal populations, including pyramidal cells in cortical layer IV.
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