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Dev Dyn. 2016 Apr;245(4):497-507. doi: 10.1002/dvdy.24389. Epub 2016 Feb 24.

Syndactyly in a novel Fras1(rdf) mutant results from interruption of signals for interdigital apoptosis.

Author information

1
Laboratory of Genetics University of Wisconsin Madison, WI, 53706.
2
Institute of Biochemistry and Cell Biology Shanghai Institute for Biological Sciences Chinese Academy of Sciences Shanghai, China, 200031.
3
Zhiyuan College Shanghai Jiao Tong University Shanghai, China, 200240.

Abstract

BACKGROUND:

Fras1 encodes an extracellular matrix protein that is critical for the establishment of the epidermal basement membrane during gestation. In humans, mutations in FRAS1 cause Fraser Syndrome (FS), a pleiotropic condition with many clinical presentations such as limb, eye, kidney, and craniofacial deformations. Many of these defects are mimicked by loss of Fras1 in mice, and are preceded by the formation of epidermal blisters in utero.

RESULTS:

In this study, we identified a novel ENU-derived rounded foot (rdf) mouse mutant with highly penetrant hindlimb soft-tissue syndactyly, among other structural defects. Mapping and sequencing revealed that rdf is a novel loss-of-function nonsense allele of Fras1 (Fras1(rdf)). Focusing on the limb, we found that the Fras1(rdf) syndactyly phenotype originates from loss of interdigital cell death (ICD). Despite normal expression of bone morphogenetic protein (BMP) ligands and their receptors, the BMP downstream target gene Msx2, which is also necessary and sufficient to promote ICD, was down-regulated in the interdigital regions of Fras1(rdf) hindlimb buds.

CONCLUSIONS:

The close correlation between limb bud epidermal blistering, decreased Msx2 expression, and reduced ICD in the Fras1(rdf) hindlimb buds suggests that epithelium detachment from the mesenchyme may create a physical gap that interrupts the transmission of BMP, among other signals, resulting in soft tissue syndactyly.

KEYWORDS:

BMP signaling; ENU screen; Fraser syndrome; interdigital cell death; limb development

PMID:
26813283
PMCID:
PMC4860343
DOI:
10.1002/dvdy.24389
[Indexed for MEDLINE]
Free PMC Article

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