Literature DB >> 14597572

Replicated anterior zeugopod (raz): a polydactylous mouse mutant with lowered Shh signaling in the limb bud.

Ottheinz Krebs1, Claire M Schreiner, William J Scott, Sheila M Bell, David J Robbins, John A Goetz, Heidi Alt, Norm Hawes, Eckhard Wolf, Jack Favor.   

Abstract

A unique limb phenotype is described in a radiation-induced mutant mouse resulting from an inversion of a proximal segment of chromosome 5. The limb phenotype in the homozygous mutant presents with two anterior skeletal elements in the zeugopod but no posterior bone, hence the name replicated anterior zeugopod, raz. The zeugopod phenotype is accompanied by symmetrical central polydactyly of hand and foot. The chromosomal inversion includes the Shh gene and the regulatory locus, located approximately 1 Mb away, within the Lmbr1 gene. In homozygous mutants, the expression of Shh mRNA and Shh protein is severely downregulated to about 20% of wild-type limb buds, but Shh expression appears normal throughout the remainder of the embryo. Correspondingly, Gli3 expression is upregulated and posteriorly expanded in the raz/raz limb bud. We propose that the double anterior zeugopod and symmetrical central polydactyly are due to an increased and uniform concentration of the Gli3 repressor form because of lowered Shh signaling.

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Year:  2003        PMID: 14597572     DOI: 10.1242/dev.00861

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  3 in total

1.  An inversion involving the mouse Shh locus results in brachydactyly through dysregulation of Shh expression.

Authors:  Michael Niedermaier; Georg C Schwabe; Stephan Fees; Anne Helmrich; Norbert Brieske; Petra Seemann; Jochen Hecht; Volkhard Seitz; Sigmar Stricker; Gundula Leschik; Evelin Schrock; Paul B Selby; Stefan Mundlos
Journal:  J Clin Invest       Date:  2005-04       Impact factor: 14.808

2.  Identification of spontaneous mutations within the long-range limb-specific Sonic hedgehog enhancer (ZRS) that alter Sonic hedgehog expression in the chicken limb mutants oligozeugodactyly and silkie breed.

Authors:  Sarah A Maas; Takayuki Suzuki; John F Fallon
Journal:  Dev Dyn       Date:  2011-05       Impact factor: 3.780

3.  Characterization of the chromosomal inversion associated with the Koa mutation in the mouse revealed the cause of skeletal abnormalities.

Authors:  Kentaro Katayama; Sayaka Miyamoto; Aki Furuno; Kouyou Akiyama; Sakino Takahashi; Hiroetsu Suzuki; Takehito Tsuji; Tetsuo Kunieda
Journal:  BMC Genet       Date:  2009-09-22       Impact factor: 2.797

  3 in total

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