Figure 5
Figure 5. Gata1 DNA binding level–dependent myeloid expansion. Lateral views of whole embryos with the head to the right and dorsal to the top. (A) Expression pattern of the myeloid markers l-plastin and mpo in 24-26 hpf gata1T301K/vlt (l-plastin, n = 9/9; mpo, n = 5/5), gata1vlt/vlt (l-plastin, n = 2/2; mpo, n = 5/5), and wild-type embryos (l-plastin, n = 6/6; mpo, n = 7/7) showing an expansion of l-plastin expression in the gata1 mutant embryos. (B) Double in situ hybridization showing l-plastin (purple staining, indicated by purple arrows) and mpo (orange staining, indicated by orange arrows) in the ICM/AGM regions of 26-30 hpf gata1T301K/vlt (n = 4/4), gata1vlt/vlt (n = 12/12) and wild-type (n = 12/12) embryos. Original magnifications ×50 (A) and ×115 (B). Individual embryos were imaged and genotyped by PCR followed by Taq1 digestion (vlt) or sequencing (T301K).

Gata1 DNA binding level–dependent myeloid expansion. Lateral views of whole embryos with the head to the right and dorsal to the top. (A) Expression pattern of the myeloid markers l-plastin and mpo in 24-26 hpf gata1T301K/vlt (l-plastin, n = 9/9; mpo, n = 5/5), gata1vlt/vlt (l-plastin, n = 2/2; mpo, n = 5/5), and wild-type embryos (l-plastin, n = 6/6; mpo, n = 7/7) showing an expansion of l-plastin expression in the gata1 mutant embryos. (B) Double in situ hybridization showing l-plastin (purple staining, indicated by purple arrows) and mpo (orange staining, indicated by orange arrows) in the ICM/AGM regions of 26-30 hpf gata1T301K/vlt (n = 4/4), gata1vlt/vlt (n = 12/12) and wild-type (n = 12/12) embryos. Original magnifications ×50 (A) and ×115 (B). Individual embryos were imaged and genotyped by PCR followed by Taq1 digestion (vlt) or sequencing (T301K).

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