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Publication : Mouse Models of <i>c-myc</i> Deregulation Driven by IgH Locus Enhancers as Models of B-Cell Lymphomagenesis.

First Author  Ferrad M Year  2020
Journal  Front Immunol Volume  11
Pages  1564 PubMed ID  32793219
Mgi Jnum  J:307927 Mgi Id  MGI:6726712
Doi  10.3389/fimmu.2020.01564 Citation  Ferrad M, et al. (2020) Mouse Models of c-myc Deregulation Driven by IgH Locus Enhancers as Models of B-Cell Lymphomagenesis. Front Immunol 11:1564
abstractText  Chromosomal translocations linking various oncogenes to transcriptional enhancers of the immunoglobulin heavy chain (IgH) locus are often implicated as the cause of B-cell malignancies. Two major IgH transcriptional enhancers have been reported so far. The Emu enhancer located upstream of the Cmu gene controls early events in B-cell maturation such as VDJ recombination. The 3' regulatory region (3'RR) located downstream from the Calpha gene controls late events in B-cell maturation such as IgH transcription, somatic hypermutation, and class switch recombination. Convincing demonstrations of the essential contributions of both Emu and 3'RR in B-cell lymphomagenesis have been provided by transgenic and knock-in animal models which bring the oncogene c-myc under Emu/3'RR transcriptional control. This short review summarizes the different mouse models so far available and their interests/limitations for progress in our understanding of human c-myc-induced B-cell lymphomagenesis.
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