scholarly journals Dsprul: A spontaneous mouse mutation in desmoplakin as a model of Carvajal-Huerta syndrome

2015 ◽  
Vol 98 (2) ◽  
pp. 164-172 ◽  
Author(s):  
C. Herbert Pratt ◽  
Christopher S. Potter ◽  
Heather Fairfield ◽  
Laura G. Reinholdt ◽  
David E. Bergstrom ◽  
...  
Keyword(s):  
1995 ◽  
Vol 15 (7) ◽  
pp. 4838-4850 ◽  
Author(s):  
RM Hoffarth ◽  
JG Johnston ◽  
LA Krushel ◽  
D van der Kooy

Development ◽  
1999 ◽  
Vol 126 (21) ◽  
pp. 4729-4736
Author(s):  
L. Lettice ◽  
J. Hecksher-Sorensen ◽  
R.E. Hill

Epithelial-mesenchymal interactions are essential for both limb outgrowth and pattern formation in the limb. Molecules capable of communication between these two tissues are known and include the signaling molecules SHH and FGF4, FGF8 and FGF10. Evidence suggests that the pattern and maintenance of expression of these genes are dependent on a number of factors including regulatory loops between genes expressed in the AER and those in the underlying mesenchyme. We show here that the mouse mutation dominant hemimelia (Dh) alters the pattern of gene expression in the AER such that Fgf4, which is normally expressed in a posterior domain, and Fgf8, which is expressed throughout are expressed in anterior patterns. We show that maintenance of Shh expression in the posterior mesenchyme is not dependent on either expression of Fgf4 or normal levels of Fgf8 in the overlying AER. Conversely, AER expression of Fgf4 is not directly dependent on Shh expression. Also the reciprocal regulatory loop proposed for Fgf8 in the AER and Fgf10 in the underlying mesenchyme is also uncoupled by this mutation. Early during the process of limb initiation, Dh is involved in regulating the width of the limb bud, the mutation resulting in selective loss of anterior mesenchyme. The Dh gene functions in the initial stages of limb development and we suggest that these initial roles are linked to mechanisms that pattern gene expression in the AER.


Chromosoma ◽  
2014 ◽  
Vol 123 (6) ◽  
pp. 529-544 ◽  
Author(s):  
Silvia Garagna ◽  
Jesus Page ◽  
Raul Fernandez-Donoso ◽  
Maurizio Zuccotti ◽  
Jeremy B. Searle
Keyword(s):  

2001 ◽  
Vol 53 (3) ◽  
pp. 233-242 ◽  
Author(s):  
Fernando Benavides ◽  
Ann Venables ◽  
Heather Poetschke Klug ◽  
Edward Glasscock ◽  
Natalia Martin Palenzuela ◽  
...  

2009 ◽  
Vol 30 (2) ◽  
pp. 119-124 ◽  
Author(s):  
Erin N. McMurray ◽  
Eric D. Rogers ◽  
Jennifer V. Schmidt

The insertional mouse mutation Adp (Acrodysplasia) confers a parent-of-origin developmental phenotype, with animals inheriting the mutation from their father showing skeletal abnormalities, whereas those inheriting the mutation from their mother are normal. This parental-specific phenotype, along with mapping of the insertion to a region of chromosome 12 proposed to contain imprinted genes, suggested that disruption of genomic imprinting might underlie the Adp phenotype. Genomic imprinting is the process by which autosomal genes are epigenetically silenced on one of the two parental alleles; imprinting mutation phenotypes manifest after inheritance from one parent but not the other. Imprinted genes typically occur in dense clusters that contain few non-imprinted genes and therefore representative genes from the Adp critical region could be assayed to identify any imprinted domains. None of the genes analysed were found to be imprinted, however, suggesting that other explanations for the Adp phenotype must be considered.


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