Figure 1
Figure 1. −2.8 kb GATA switch site regulates Gata2 expression in hematopoietic stem and progenitor cells, but is dispensible in erythroid cells. Gata2 expression within LT-HSC and MPP populations (LT-HSC defined as Lindimckit+Sca1+CD150+ and MPP defined as Lindimckit+Sca1+CD34+ or Lindimckit+Sca1+CD150−) from E12.5 fetal livers normalized to β-actin (A). Frequencies of LT-HSCs and MPPs in wild-type and Δ-2.8 fetal livers (B). Gata2 expression within CMP and MEP populations (with CMP defined as LindimSca1−,c-kit+CD34+, FcγR− and MEP defined as Lindim Sca1−c-kit+CD34−, FcγR−) from E12.5 fetal livers normalized to β-actin (C). Frequencies of CMPs and MEPs from wild-type and Δ-2.8 fetal livers (D). Gata2 expression was assessed by qPCR in Stage I through Stage IV sorted erythroid cells, corresponding to CD71loTer119− (committed erythroid progenitors, Stage I), CD71hiTer119− (proerythroblasts, Stage II), CD71hiTer119+ (basophilic erythroblasts, Stage III), and CD71loTer119+ (late erythroblasts, Stage IV) from wild-type and Δ-2.8 embryos. (E). Relative number of cells in Stage I-IV was determined in wild-type and Δ-2.8 E13.5 fetal liver cells, based on CD71 and Ter119 expression (F). Mean ± SEM. Statistical significance was assessed by 2-sided Student t test. *P ≤ .05 and **P ≤ .01.

−2.8 kb GATA switch site regulates Gata2 expression in hematopoietic stem and progenitor cells, but is dispensible in erythroid cells. Gata2 expression within LT-HSC and MPP populations (LT-HSC defined as Lindimckit+Sca1+CD150+ and MPP defined as Lindimckit+Sca1+CD34+ or Lindimckit+Sca1+CD150) from E12.5 fetal livers normalized to β-actin (A). Frequencies of LT-HSCs and MPPs in wild-type and Δ-2.8 fetal livers (B). Gata2 expression within CMP and MEP populations (with CMP defined as LindimSca1,c-kit+CD34+, FcγR and MEP defined as Lindim Sca1c-kit+CD34, FcγR) from E12.5 fetal livers normalized to β-actin (C). Frequencies of CMPs and MEPs from wild-type and Δ-2.8 fetal livers (D). Gata2 expression was assessed by qPCR in Stage I through Stage IV sorted erythroid cells, corresponding to CD71loTer119 (committed erythroid progenitors, Stage I), CD71hiTer119 (proerythroblasts, Stage II), CD71hiTer119+ (basophilic erythroblasts, Stage III), and CD71loTer119+ (late erythroblasts, Stage IV) from wild-type and Δ-2.8 embryos. (E). Relative number of cells in Stage I-IV was determined in wild-type and Δ-2.8 E13.5 fetal liver cells, based on CD71 and Ter119 expression (F). Mean ± SEM. Statistical significance was assessed by 2-sided Student t test. *P ≤ .05 and **P ≤ .01.

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