Bamforth, SD and Braganca, J and Farthing, CR and Schneider, JE and Broadbent, C and Michell, AC and Clarke, K and Neubauer, S and Norris, D and Brown, NA and Anderson, RH and Bhattacharya, S (2004) Cited2 controls left-right patterning and heart development through a Nodal-Pitx2c pathway. Nature Genetics , 36 (11) 1189 - 1196. 10.1038/ng1446.
Full text not available from this repository.
Malformations of the septum, outflow tract and aortic arch are the most common congenital cardiovascular defects and occur in mice lacking Cited2, a transcriptional coactivator of TFAP2. Here we show that Cited2(-/-) mice also develop laterality defects, including right isomerism, abnormal cardiac looping and hyposplenia, which are suppressed on a mixed genetic background. Cited2(-/-) mice lack expression of the Nodal target genes Pitx2c, Nodal and Ebaf in the left lateral plate mesoderm, where they are required for establishing laterality and cardiovascular development. CITED2 and TFAP2 were detected at the Pitx2c promoter in embryonic hearts, and they activate Pitx2c transcription in transient transfection assays. We propose that an abnormal Nodal-Pitx2c pathway represents a unifying mechanism for the cardiovascular malformations observed in Cited2(-/-) mice, and that such malformations may be the sole manifestation of a laterality defect
|Title:||Cited2 controls left-right patterning and heart development through a Nodal-Pitx2c pathway|
|Additional information:||WoS ID: 000224832800022 JournalNOV867HINAT GENET|
|Keywords:||A, abnormal, AND, CARDIAC, cardiovascular, congenital, CONTROL, DEFECT, DEFECTS, development, EXPRESSION, FOR, GENE, Genes, Genetic, HEART, Isomerism, JOURNAL, Laterality, malformation, Malformations, Mechanism, Mesoderm, MICE, OF, PATHWAY, PLATE, right isomerism, THE, TRACT, TRANSCRIPTION, Transfection|
|UCL classification:||UCL > School of Life and Medical Sciences > Faculty of Population Health Sciences > Institute of Child Health|
Archive Staff Only: edit this record