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Lookup NU author(s): Dr Simon BamforthORCiD
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Deletion of the transcriptional modulator Cited2 in the mouse results in embryonic lethality, cardiovascularmalformations, adrenal agenesis, cranial ganglia fusion, exencephaly, and left–right patterningdefects, all seen with a varying degree of penetrance. The phenotypic heterogeneity, observed on differentgenetic backgrounds, indicates the existence of both genetic and environmental modifiers. Mice lackingthe LIM domain-containing protein Lmo4 share specific phenotypes with Cited2 null embryos, such as embryoniclethality, cranial ganglia fusion, and exencephaly. These shared phenotypes suggested that Lmo4may be a potential genetic modifier of the Cited2 phenotype. Examination of Lmo4-deficient embryosrevealed partially penetrant cardiovascular malformations and hypoplastic thymus. Examination ofLmo4;Cited2 compound mutants indicated that there is a genetic interaction between Cited2 and Lmo4 incontrol of thymus development. Our data suggest that this may occur, in part, through control of expressionof a common target gene, Tbx1, which is necessary for normal thymus development.
Author(s): Michell A, Braganca J, Broadbent C, Joyce B, Franklyn A, Schneider JE, Bhattacharya S, Bamforth SD
Publication type: Article
Publication status: Published
Journal: Developmental Dynamics
Year: 2010
Volume: 239
Issue: 7
Pages: 1988-1994
Print publication date: 28/05/2010
ISSN (print): 1058-8388
ISSN (electronic): 1097-0177
Publisher: John Wiley & Sons, Inc.
URL: http://dx.doi.org/10.1002/dvdy.22334
DOI: 10.1002/dvdy.22334
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