Article ID: 19-0137
The transcription factor c-Maf is a member of the large Maf family, members of which possess transactivation and bZIP domains. c-Maf plays an important role in lens formation, T-lymphocyte differentiation, hypertrophic chondrocyte differentiation, and kidney development in mouse embryos. However, because homozygous deletion of c-Maf in C57BL/6J mice causes embryonic lethality, the functions of c-Maf in adult mice remain largely uninvestigated. To address this issue, we generated c-Maf floxed (c-Maffl/fl) C57BL/6J mice and established tamoxifen-inducible c-Maf knockout mice (c-Maffl/fl; CAG-Cre-ERTMmice, c-MafΔTAM). After tamoxifen injection, adult c-MafΔTAMmice showed successful deletion of c-Maf protein and developed severe cataracts; cataracts are also seen in human patients who have mutations in the c-MAF DNA binding domain. Furthermore, adult c-MafΔTAMmice exhibited abnormal lens structure and impaired differentiation of lens fiber cells. In summary, we established c-Maffl/fland c-MafΔTAMC57BL/6J mice, which can be useful animal models for the investigation of c-Maf function in various developmental stages and can also be used as a disease model for cataracts.