Manipulation of mouse hematopoietic progenitors by specific retroviral infection
Research output: Contribution to journal › Article
Colleges, School and Institutes
Previous studies have identified an enhancer 3' of the scl gene that can direct transgene expression to hematopoietic progenitors and stem cells. Here we use this enhancer to restrict expression of the avian leukosis virus receptor, TVA, to hematopoietic stem cells and progenitors in bone marrow and fetal liver and demonstrate that retroviral infection can be used to specifically introduce exogenous sequences. We show that a majority of CFU-S-12 multipotential progenitor cells can be transduced in vitro. Uniquely, transduction of TVA(+) progenitors with a retrovirus encoding a puromycin resistance gene allows selection and expansion of a multipotential hematopoietic progenitor population that can be superinfected with high efficiency. Using this system we show for the first time that v-Myb oncoproteins expressed from avian viruses can induce a leukemic transformation in the mouse. The phenotype of the transformed cells is similar to that which is seen in the chicken and is likewise dependent on the particular structure of v-Myb. This implies that the basic mechanisms of action of mutated transcription factors in the etiology of leukemia are conserved between birds and mammals.
|Number of pages||8|
|Journal||Journal of Biological Chemistry|
|Early online date||11 Aug 2003|
|Publication status||Published - 1 Oct 2003|