Figure 6
Figure 6. The effects of Lsd1 conditional inactivation on erythropoiesis and chromatin occupancy by TR2 and TR4 and corepressors. (A) Lsd1f/f Lin− BM cells were mock-infected (Cre−) or infected with Ad-Cre (Cre+) on days 0 and 2 of culture. An aliquot of cells was stained daily with anti-CD71 and anti-Ter119 antibodies prior to flow cytometric analyses. Conditional loss of Lsd1 in Lin− BM cells, which had been exposed to Ad-Cre infection, led to far fewer mature CD71−Ter119+ cells and an increased number of immature CD71+Ter119+ cells. (B-E) LSD1 inactivation obliterated its chromatin occupancy, as expected, and of its partner CoREST. The binding of TR2/TR4 and other corepressor components to the β-type globin gene promoters were either unchanged or quite modestly reduced in infected Lsd1f/f Lin− cells.

The effects of Lsd1 conditional inactivation on erythropoiesis and chromatin occupancy by TR2 and TR4 and corepressors. (A) Lsd1f/f Lin BM cells were mock-infected (Cre) or infected with Ad-Cre (Cre+) on days 0 and 2 of culture. An aliquot of cells was stained daily with anti-CD71 and anti-Ter119 antibodies prior to flow cytometric analyses. Conditional loss of Lsd1 in Lin BM cells, which had been exposed to Ad-Cre infection, led to far fewer mature CD71Ter119+ cells and an increased number of immature CD71+Ter119+ cells. (B-E) LSD1 inactivation obliterated its chromatin occupancy, as expected, and of its partner CoREST. The binding of TR2/TR4 and other corepressor components to the β-type globin gene promoters were either unchanged or quite modestly reduced in infected Lsd1f/f Lin cells.

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