期刊
NATURE GENETICS
卷 41, 期 9, 页码 977-U40出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/ng.435
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资金
- NICHD NIH HHS [R01 HD055300-01, R01 HD055300, R01HD055300, R01 HD055300-03, R01 HD055300-02] Funding Source: Medline
- NIMH NIH HHS [K08 MH001750-05, K08MH001750, K08 MH001750-04, K08 MH001750-03] Funding Source: Medline
- EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT [R01HD055300] Funding Source: NIH RePORTER
- NATIONAL INSTITUTE OF MENTAL HEALTH [K08MH001750] Funding Source: NIH RePORTER
Mice homozygous for mutations in Dact1 (also called Dapper or Frodo) phenocopy human malformations involving the spine, genitourinary system and distal digestive tract. We traced this phenotype to disrupted germ-layer morphogenesis at the primitive streak. Notably, heterozygous mutation of Vangl2, a transmembrane component of the planar cell polarity (PCP) pathway, rescued recessive Dact1 phenotypes, whereas loss of Dact1 reciprocally rescued semidominant Vangl2 phenotypes. We show that Dact1, an intracellular protein, forms a complex with Vangl2. In Dact1 mutants, Vangl2 was increased at the primitive streak, where cells ordinarily undergo an epithelial-mesenchymal transition. This is associated with abnormal E-cadherin distribution and changes in biochemical measures of the PCP pathway. We conclude that Dact1 contributes to morphogenesis at the primitive streak by regulating Vangl2 upstream of cell adhesion and the PCP pathway.
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