Literature DB >> 1983115

Evidence for allelism of the recessive insertional mutation add and the dominant mouse mutation extra-toes (Xt).

T M Pohl1, M G Mattei, U Rüther.   

Abstract

A recessive mutant caused by insertional mutagenesis in transgenic mice has been detected in which the anterior part of the forelimb is disorganized. The morphology of the thumb is always altered and sometimes the adjacent finger has an extra phalanx. This phenotype suggests that a body plan gene is affected. We have named the mutation add (anterior digit-pattern deformity). Using the cloned DNA from the flanking region of the integrated transgene, add has been mapped close to the centromere of chromosome 13. This position links add to a genetically mapped locus called extra-toes (Xt). The phenotype of the double-mutant add/Xt as well as the molecular analysis suggest that add and Xt are allelic.

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Year:  1990        PMID: 1983115     DOI: 10.1242/dev.110.4.1153

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


  18 in total

1.  Inherited haemolytic anaemia created by insertional inactivation of the alpha-spectrin gene.

Authors:  G Grimber; C Galand; M Garbarz; M G Mattei; C Cavard; A Zider; P Blanchet; P Boivin; P Briand; D Dhermy
Journal:  Transgenic Res       Date:  1992-11       Impact factor: 2.788

Review 2.  Mouse chromosome 13.

Authors:  M J Justice; D A Stephenson
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

3.  The same genomic region is disrupted in two transgene-induced limb deformity alleles.

Authors:  T F Vogt; L Jackson-Grusby; A J Wynshaw-Boris; D C Chan; P Leder
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

Review 4.  Mouse chromosome 13.

Authors:  M J Justice; D A Stephenson
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

5.  The bst locus on mouse chromosome 16 is associated with age-related subretinal neovascularization.

Authors:  R S Smith; S W John; A Zabeleta; M T Davisson; N L Hawes; B Chang
Journal:  Proc Natl Acad Sci U S A       Date:  2000-02-29       Impact factor: 11.205

6.  Molecular linkage of the morphogenetic mutation add and the zinc finger gene Gli3.

Authors:  F van der Hoeven; T Schimmang; A Vortkamp; U Rüther
Journal:  Mamm Genome       Date:  1993       Impact factor: 2.957

7.  The development of the eye in homozygotes of the mouse mutant Extra-toes.

Authors:  T Franz; A Besecke
Journal:  Anat Embryol (Berl)       Date:  1991

8.  The mouse mutant Polydactyly Nagoya (Pdn) defines a novel allele of the zinc finger gene Gli3.

Authors:  T Schimmang; S I Oda; U Rüther
Journal:  Mamm Genome       Date:  1994-06       Impact factor: 2.957

9.  Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt).

Authors:  A Vortkamp; T Franz; M Gessler; K H Grzeschik
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

Review 10.  Insertional mutagenesis in transgenic mice.

Authors:  T Rijkers; A Peetz; U Rüther
Journal:  Transgenic Res       Date:  1994-07       Impact factor: 2.788

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