Titomirov A V, Pereverzev A E, Stepan'ian L I, Podgornaia O I, Aprelikova O N
Tsitologiia. 1985 Oct;27(10):1183-8.
Introduction of the plasmid containing the methotrexate-resistant (Mtx-r) bacterial gene of dihydrofolate reductase (DHFR) under the control of the early promoter of SV 40 into the donor bone cells of the mouse with subsequent transplantation of the cells into lethally irradiated mice results in the increase in the life span of mice under conditions of methotrexate selection. It is due to the stable transformation of the bone marrow colony-forming cells with the plasmic DNA and the synthesis of the bacterial Mtx-r DHFR in the spleen and bone marrow of the recipient mouse.
将含有在SV 40早期启动子控制下的二氢叶酸还原酶(DHFR)的甲氨蝶呤抗性(Mtx-r)细菌基因的质粒导入小鼠的供体骨细胞,随后将这些细胞移植到经致死剂量照射的小鼠体内,结果在甲氨蝶呤选择条件下小鼠的寿命延长。这是由于骨髓集落形成细胞被质粒DNA稳定转化,以及受体小鼠的脾脏和骨髓中合成了细菌Mtx-r DHFR。