We produced transgenic mice using SV40 Tag gene under the control of i
ts own enhancer and promoter. Three transgenic lines (SNU-SVT125, 127,
248) consistently developed thymic carcinoma as well as choroid plexu
s carcinoma and dysplastic renal tubule. In SNU-SVT248 line, SV40 Tag
transgene was expressed at thymus, spleen and kidney. Thymic epitheliu
m showed high level expression of SV40 Tag in immunohistochemistry. Hi
stopathological and electron microscopic analysis revealed that poorly
differentiated carcinoma was derived from type 2 to 4 thymic epitheli
al cell. Our transgenic mice would provide a model for studies on the
pathogenesis of thymic carcinoma and on the regulation of thymopoiesis
by epithelial cells.