| First Author | Brooke-Bisschop T | Year | 2017 |
| Journal | Dev Biol | Volume | 422 |
| Issue | 2 | Pages | 115-124 |
| PubMed ID | 28065741 | Mgi Jnum | J:239299 |
| Mgi Id | MGI:5828306 | Doi | 10.1016/j.ydbio.2017.01.002 |
| Citation | Brooke-Bisschop T, et al. (2017) Essential roles for Cdx in murine primitive hematopoiesis. Dev Biol 422(2):115-124 |
| abstractText | 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. |
