Literature DB >> 7550316

Interaction between undulated and Patch leads to an extreme form of spina bifida in double-mutant mice.

U Helwig1, K Imai, W Schmahl, B E Thomas, D S Varnum, J H Nadeau, R Balling.   

Abstract

The aetiology of spina bifida involves genetic and environmental factors, which may be why major genes contributing to pathogenesis have not been identified. Here we report that undulated-Patch double-mutant mice have a phenotype reminiscent of an extreme form of spina bifida occulta in humans. This unexpected phenotype in double-mutant but not single-mutant mice shows that novel congenital anomalies such as spina bifida can result from interaction between products of independently segregating loci. This example of digenic inheritance may explain the often sporadic nature of spina bifida in humans.

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Year:  1995        PMID: 7550316     DOI: 10.1038/ng0995-60

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


  12 in total

1.  Tint maps to mouse chromosome 6 and may interact with a notochordal enhancer of Brachyury.

Authors:  Jiang I Wu; M A Centilli; Gabriela Vasquez; Susan Young; Jonathan Scolnick; Larissa A Durfee; Jimmy L Spearow; Staci D Schwantz; Gabriela Rennebeck; Karen Artzt
Journal:  Genetics       Date:  2007-10       Impact factor: 4.562

Review 2.  The role of the laboratory mouse in the human genome project.

Authors:  M H Meisler
Journal:  Am J Hum Genet       Date:  1996-10       Impact factor: 11.025

3.  Promotor genotype of the platelet-derived growth factor receptor-alpha gene shows population stratification but not association with spina bifida meningomyelocele.

Authors:  K-S Au; H Northrup; T J Kirkpatrick; K A Volcik; J M Fletcher; I T Townsend; S H Blanton; G H Tyerman; G Villarreal; T M King
Journal:  Am J Med Genet A       Date:  2005-12-15       Impact factor: 2.802

4.  PAX genes and human neural tube defects: an amino acid substitution in PAX1 in a patient with spina bifida.

Authors:  F A Hol; M P Geurds; S Chatkupt; Y Y Shugart; R Balling; C T Schrander-Stumpel; W G Johnson; B C Hamel; E C Mariman
Journal:  J Med Genet       Date:  1996-08       Impact factor: 6.318

5.  Altered regulation of platelet-derived growth factor receptor-alpha gene-transcription in vitro by spina bifida-associated mutant Pax1 proteins.

Authors:  P H Joosten; F A Hol; S E van Beersum; H Peters; B C Hamel; G B Afink; E J van Zoelen; E C Mariman
Journal:  Proc Natl Acad Sci U S A       Date:  1998-11-24       Impact factor: 11.205

6.  Mouse Brachyury the Second (T2) is a gene next to classical T and a candidate gene for tct.

Authors:  G Rennebeck; E Lader; A Fujimoto; E P Lei; K Artzt
Journal:  Genetics       Date:  1998-11       Impact factor: 4.562

7.  Overlapping roles for homeodomain-interacting protein kinases hipk1 and hipk2 in the mediation of cell growth in response to morphogenetic and genotoxic signals.

Authors:  Kyoichi Isono; Kazumi Nemoto; Yuanyuan Li; Yuki Takada; Rie Suzuki; Motoya Katsuki; Akira Nakagawara; Haruhiko Koseki
Journal:  Mol Cell Biol       Date:  2006-04       Impact factor: 4.272

8.  Temporal and spatial specificity of PDGF alpha receptor promoter in transgenic mice.

Authors:  K K Reinertsen; R T Bronson; C D Stiles; C Wang
Journal:  Gene Expr       Date:  1997

9.  Disruption of PDGFRalpha-initiated PI3K activation and migration of somite derivatives leads to spina bifida.

Authors:  Elizabeth A Pickett; Gregory S Olsen; Michelle D Tallquist
Journal:  Development       Date:  2008-02       Impact factor: 6.868

10.  Pax3 modulates expression of the c-Met receptor during limb muscle development.

Authors:  J A Epstein; D N Shapiro; J Cheng; P Y Lam; R L Maas
Journal:  Proc Natl Acad Sci U S A       Date:  1996-04-30       Impact factor: 11.205

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