کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5531697 | 1401808 | 2017 | 10 صفحه PDF | دانلود رایگان |

- Loss of Cdx disrupts murine primitive hematopoiesis and vasculogenesis.
- This phenotype manifests in the endothelial/primitive hematopoietic lineages.
- The phenotype is associated with attenuation of Scl/Tal1 expression.
- Cdx2 occupies the Scl promoter in vivo.
- Exogenous Scl rescues Cdx-dependent hematopoietic defects.
The Cdx transcription factors play essential roles in primitive hematopoiesis in the zebrafish where they exert their effects, in part, through regulation of hox genes. Defects in hematopoiesis have also been reported in Cdx mutant murine embryonic stem cell models, however, to date no mouse model reflecting the zebrafish Cdx mutant hematopoietic phenotype has been described. This is likely due, in part, to functional redundancy among Cdx members and the early lethality of Cdx2 null mutants. To circumvent these limitations, we used Cre-mediated conditional deletion to assess the impact of concomitant loss of Cdx1 and Cdx2 on murine primitive hematopoiesis. We found that Cdx1/Cdx2 double mutants exhibited defects in primitive hematopoiesis and yolk sac vasculature concomitant with reduced expression of several genes encoding hematopoietic transcription factors including Scl/Tal1. Chromatin immunoprecipitation analysis revealed that Scl was occupied by Cdx2 in vivo, and Cdx mutant hematopoietic yolk sac differentiation defects could be rescued by expression of exogenous Scl. These findings demonstrate critical roles for Cdx members in murine primitive hematopoiesis upstream of Scl.
Journal: Developmental Biology - Volume 422, Issue 2, 15 February 2017, Pages 115-124