Literature DB >> 8620844

A mutational analysis of the 5' HoxD genes: dissection of genetic interactions during limb development in the mouse.

A P Davis1, M R Capecchi.   

Abstract

Using gene targeting in mice, we have undertaken a systematic mutational analysis of the homeobox-containing 5' HoxD genes. In particular, we have characterized the limb defects observed in mice with independent targeted disruptions of hoxd-12 and hoxd-13. Animals defective for hoxd-12 are viable, fertile, and appear outwardly normal yet have minor autopodal defects in the forelimb which include a reduction in the bone length of metacarpals and phalanges, and a malformation of the distal carpal bone d4. The limb phenotypes observed in hoxd-13 mutant mice are more extensive, including strong reductions in length, complete absences, or improper segmentations of many metacarpal and phalangeal bones. Additionally, the d4 carpal bone is not properly formed and often produces an extra rudimentary digit. To examine the genetic interactions between the 5' HoxD genes, we bred these mutant strains with each other and with our previously characterized hoxd-11 mouse to produce a series of trans-heterozygotes. Skeletal analyses of these mice reveal that these genes interact in the formation of the vertebrate limb, since the trans-heterozygotes display phenotypes not present in the individual heterozygotes, including more severe carpal, metacarpal and phalangeal defects. Some of these phenotypes appear to be accounted for by a delay in the ossification events in the autopod, which lead to either the failure of fusion or the elimination of cartilaginous elements. Characteristically, these mutations lead to the overall truncation of digits II and V on the forelimb. Additionally, some trans-animals show the growth of an extra postaxial digit VI, which is composed of a bony element resembling a phalange. The results demonstrate that these genes interact in the formation of the limb. In addition to the previously characterized paralogous interactions, a multitude of interactions between Hox genes is used to finely sculpt the forelimb. The 5' Hox genes could therefore act as a major permissive genetic milieu that has been exploited by evolutionary adaptation to form the tetrapod limbs.

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Year:  1996        PMID: 8620844     DOI: 10.1242/dev.122.4.1175

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


  48 in total

1.  Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formation.

Authors:  Pablo Villavicencio-Lorini; Pia Kuss; Julia Friedrich; Julia Haupt; Muhammed Farooq; Seval Türkmen; Denis Duboule; Jochen Hecht; Stefan Mundlos
Journal:  J Clin Invest       Date:  2010-05-10       Impact factor: 14.808

Review 2.  Genetic disorders of the skeleton: a developmental approach.

Authors:  Uwe Kornak; Stefan Mundlos
Journal:  Am J Hum Genet       Date:  2003-07-31       Impact factor: 11.025

3.  Nonsyndromic brachydactyly type D and type E mapped to 7p15 in healthy children and adults from the Jirel ethnic group in eastern Nepal.

Authors:  Kimberly D Williams; John Blangero; Janardan Subedi; Bharat Jha; Thomas Dyer; John L Vandeberg; Bradford Towne; Sarah Williams-Blangero
Journal:  Am J Hum Biol       Date:  2013-09-10       Impact factor: 1.937

Review 4.  Sometimes the result is not the answer: the truths and the lies that come from using the complementation test.

Authors:  R Scott Hawley; William D Gilliland
Journal:  Genetics       Date:  2006-09       Impact factor: 4.562

5.  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 6.  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

7.  A conserved role for Hox paralog group 4 in regulation of hematopoietic progenitors.

Authors:  Michelina Iacovino; Carmen Hernandez; Zhaohui Xu; Gagan Bajwa; Melissa Prather; Michael Kyba
Journal:  Stem Cells Dev       Date:  2009-06       Impact factor: 3.272

8.  Paralogous mouse Hox genes, Hoxa9, Hoxb9, and Hoxd9, function together to control development of the mammary gland in response to pregnancy.

Authors:  F Chen; M R Capecchi
Journal:  Proc Natl Acad Sci U S A       Date:  1999-01-19       Impact factor: 11.205

9.  Evidence for at least six Hox clusters in the Japanese lamprey (Lethenteron japonicum).

Authors:  Tarang K Mehta; Vydianathan Ravi; Shinichi Yamasaki; Alison P Lee; Michelle M Lian; Boon-Hui Tay; Sumanty Tohari; Seiji Yanai; Alice Tay; Sydney Brenner; Byrappa Venkatesh
Journal:  Proc Natl Acad Sci U S A       Date:  2013-09-16       Impact factor: 11.205

10.  Evidence for regulation of cartilage differentiation by the homeobox gene Hoxc-8.

Authors:  Y G Yueh; D P Gardner; C Kappen
Journal:  Proc Natl Acad Sci U S A       Date:  1998-08-18       Impact factor: 11.205

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