Literature DB >> 8673126

The molecular basis of hypodactyly (Hd): a deletion in Hoxa 13 leads to arrest of digital arch formation.

D P Mortlock1, L C Post, J W Innis.   

Abstract

Hypodactyly (Hd) is a semidominant mutation in mice that maps in a genetic interval overlapping the Hoxa cluster. The profound deficiency of digital arch structures in Hd/Hd mice is consistent with a defect in a gene activated late in limb morphogenesis. We have determined the structure of the Hoxa13 gene and describe a 50-base pair deletion in the first exon of the Hd allele that probably arose from unequal recombination or misalignment between triplet repeats. It is predicted that no Hoxa13 protein is made from Hd mRNA. The hypodactyly limb phenotype is similar to that of Hoxd13-deficient mice in sharing defects along multiple axes and alterations in cartilage maturation; however, the overall effects on digital arch formation are more severe in Hd/Hd mice. Our results confirm the critical role of AbdB-like Hox genes in the development of the autopod, and add to the spectrum of mutations involving triplet repeats.

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Year:  1996        PMID: 8673126     DOI: 10.1038/ng0796-284

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  24 in total

1.  Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome.

Authors:  F R Goodman; C Bacchelli; A F Brady; L A Brueton; J P Fryns; D P Mortlock; J W Innis; L B Holmes; A E Donnenfeld; M Feingold; F A Beemer; R C Hennekam; P J Scambler
Journal:  Am J Hum Genet       Date:  2000-06-05       Impact factor: 11.025

2.  Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract.

Authors:  F R Goodman; S Mundlos; Y Muragaki; D Donnai; M L Giovannucci-Uzielli; E Lapi; F Majewski; J McGaughran; C McKeown; W Reardon; J Upton; R M Winter; B R Olsen; P J Scambler
Journal:  Proc Natl Acad Sci U S A       Date:  1997-07-08       Impact factor: 11.205

Review 3.  Molecular basis for skeletal variation: insights from developmental genetic studies in mice.

Authors:  C Kappen; A Neubüser; R Balling; R Finnell
Journal:  Birth Defects Res B Dev Reprod Toxicol       Date:  2007-12

4.  Attenuation of bone morphogenetic protein signaling during amphibian limb development results in the generation of stage-specific defects.

Authors:  Tamsin E M Jones; Robert C Day; Caroline W Beck
Journal:  J Anat       Date:  2013-08-28       Impact factor: 2.610

5.  Congenital anomalies and childhood cancer in Great Britain.

Authors:  S A Narod; M M Hawkins; C M Robertson; C A Stiller
Journal:  Am J Hum Genet       Date:  1997-03       Impact factor: 11.025

6.  Genetic and physical mapping of the mouse Ulnaless locus.

Authors:  C L Peichel; C M Abbott; T F Vogt
Journal:  Genetics       Date:  1996-12       Impact factor: 4.562

7.  Monodactylous limbs and abnormal genitalia are associated with hemizygosity for the human 2q31 region that includes the HOXD cluster.

Authors:  M Del Campo; M C Jones; A N Veraksa; C J Curry; K L Jones; J T Mascarello; Z Ali-Kahn-Catts; T Drumheller; W McGinnis
Journal:  Am J Hum Genet       Date:  1999-07       Impact factor: 11.025

8.  Association of MSX1 and TGFB3 with nonsyndromic clefting in humans.

Authors:  A C Lidral; P A Romitti; A M Basart; T Doetschman; N J Leysens; S Daack-Hirsch; E V Semina; L R Johnson; J Machida; A Burds; T J Parnell; J L Rubenstein; J C Murray
Journal:  Am J Hum Genet       Date:  1998-08       Impact factor: 11.025

Review 9.  Hox in hair growth and development.

Authors:  Alexander Awgulewitsch
Journal:  Naturwissenschaften       Date:  2003-04-26

10.  Opposite phenotypes of hypomorphic and Y766 phosphorylation site mutations reveal a function for Fgfr1 in anteroposterior patterning of mouse embryos.

Authors:  J Partanen; L Schwartz; J Rossant
Journal:  Genes Dev       Date:  1998-08-01       Impact factor: 11.361

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