Targeted disruption of p185/Cul7 gene results in abnormal vascular morphogenesis

T Arai, JS Kasper, JR Skaar, SH Ali… - Proceedings of the …, 2003 - National Acad Sciences
T Arai, JS Kasper, JR Skaar, SH Ali, C Takahashi, JA DeCaprio
Proceedings of the National Academy of Sciences, 2003National Acad Sciences
Cul1, a member of the cullin ubiquitin ligase family, forms a multiprotein complex known as
SCF and plays an essential role in numerous cellular and biological activities. A Cul1
homologue, p185 (Cul7), has been isolated as an simian virus 40 large T antigen-binding
protein. To understand the physiological role of p185, we generated mice lacking p185.
p185–/–embryos are runted and die immediately after birth because of respiratory distress.
Dermal and hypodermal hemorrhage is detected in mutant embryos at late gestational …
Cul1, a member of the cullin ubiquitin ligase family, forms a multiprotein complex known as SCF and plays an essential role in numerous cellular and biological activities. A Cul1 homologue, p185 (Cul7), has been isolated as an simian virus 40 large T antigen-binding protein. To understand the physiological role of p185, we generated mice lacking p185. p185/ embryos are runted and die immediately after birth because of respiratory distress. Dermal and hypodermal hemorrhage is detected in mutant embryos at late gestational stage. p185/ placentas show defects in the differentiation of the trophoblast lineage with an abnormal vascular structure. We demonstrate that p185 forms an SCF-like complex with Skp1, Rbx1, Fbw6 (Fbx29), and FAP68 (FAP48, glomulin). FAP68 has recently been identified as a gene responsible for familial glomuvenous malformation. These results suggest that p185 forms a multiprotein complex and plays an important role in vascular morphogenesis.
National Acad Sciences