Literature DB >> 8358169

A new Pax gene, Pax-9, maps to mouse chromosome 12.

J Wallin1, Y Mizutani, K Imai, N Miyashita, K Moriwaki, M Taniguchi, H Koseki, R Balling.   

Abstract

Members of the Pax gene family have recently been shown to play important roles in mouse embryogenesis. Of eight so far characterized Pax genes, three have been associated with mouse developmental mutants. Here we report the cloning of a new Pax gene, Pax-9. Most of the DNA sequence encoding the highly conserved paired domain has been determined and compared with previously known paired domains. This comparison classifies Pax-9 as a member of the same subgroup as Pax-1/undulated. By analysis of the segregation of a Pax-9 restriction fragment length polymorphism and a large number of simple sequence length polymorphisms in an interspecific C57BL/6 x Mus musculus mollosinus backcross, Pax-9 was mapped close to the D12Nds1 locus on the proximal part of Chromosome (Chr) 12.

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Year:  1993        PMID: 8358169     DOI: 10.1007/bf00360584

Source DB:  PubMed          Journal:  Mamm Genome        ISSN: 0938-8990            Impact factor:   2.957


  21 in total

1.  A genetic map of the mouse suitable for typing intraspecific crosses.

Authors:  W Dietrich; H Katz; S E Lincoln; H S Shin; J Friedman; N C Dracopoli; E S Lander
Journal:  Genetics       Date:  1992-06       Impact factor: 4.562

Review 2.  Pax in development.

Authors:  P Gruss; C Walther
Journal:  Cell       Date:  1992-05-29       Impact factor: 41.582

3.  Conservation of a large protein domain in the segmentation gene paired and in functionally related genes of Drosophila.

Authors:  D Bopp; M Burri; S Baumgartner; G Frigerio; M Noll
Journal:  Cell       Date:  1986-12-26       Impact factor: 41.582

4.  Splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3.

Authors:  D J Epstein; M Vekemans; P Gros
Journal:  Cell       Date:  1991-11-15       Impact factor: 41.582

5.  The paired box encodes a second DNA-binding domain in the paired homeo domain protein.

Authors:  J Treisman; E Harris; C Desplan
Journal:  Genes Dev       Date:  1991-04       Impact factor: 11.361

6.  Genomic sequencing.

Authors:  G M Church; W Gilbert
Journal:  Proc Natl Acad Sci U S A       Date:  1984-04       Impact factor: 11.205

7.  Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene.

Authors:  M Tassabehji; A P Read; V E Newton; R Harris; R Balling; P Gruss; T Strachan
Journal:  Nature       Date:  1992-02-13       Impact factor: 49.962

8.  An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome.

Authors:  C T Baldwin; C F Hoth; J A Amos; E O da-Silva; A Milunsky
Journal:  Nature       Date:  1992-02-13       Impact factor: 49.962

9.  Murine developmental control genes.

Authors:  M Kessel; P Gruss
Journal:  Science       Date:  1990-07-27       Impact factor: 47.728

10.  Isolation of two tissue-specific Drosophila paired box genes, Pox meso and Pox neuro.

Authors:  D Bopp; E Jamet; S Baumgartner; M Burri; M Noll
Journal:  EMBO J       Date:  1989-11       Impact factor: 11.598

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  12 in total

1.  A novel dysmorphic syndrome with open calvarial sutures and sutural cataracts maps to chromosome 14q13-q21.

Authors:  Simeon A Boyadjiev; Cristina M Justice; Wafaa Eyaid; Victor A McKusick; Ralph S Lachman; Arnab B Chowdry; Monzer Jabak; Johan Zwaan; Alexander F Wilson; Ethylin Wang Jabs
Journal:  Hum Genet       Date:  2003-04-03       Impact factor: 4.132

Review 2.  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

3.  Isolation of the Pax9 cDNA from adult human esophagus.

Authors:  H Peters; G Schuster; A Neubüser; T Richter; H Höfler; R Balling
Journal:  Mamm Genome       Date:  1997-01       Impact factor: 2.957

4.  Developmental dynamics of occipital and cervical somites.

Authors:  Anja Maschner; Stefanie Krück; Margarethe Draga; Felicitas Pröls; Martin Scaal
Journal:  J Anat       Date:  2016-07-06       Impact factor: 2.610

5.  Evolution of mouse T-box genes by tandem duplication and cluster dispersion.

Authors:  S I Agulnik; N Garvey; S Hancock; I Ruvinsky; D L Chapman; I Agulnik; R Bollag; V Papaioannou; L M Silver
Journal:  Genetics       Date:  1996-09       Impact factor: 4.562

6.  Fine genetic mapping defines the genetic order of Pax9, Tcf3a, and Acrodysplasia (Adp).

Authors:  T Watanabe; E Tarttelin; A Neubüser; M Kimura; D Solter
Journal:  Mamm Genome       Date:  1994-12       Impact factor: 2.957

7.  Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities.

Authors:  H Peters; A Neubüser; K Kratochwil; R Balling
Journal:  Genes Dev       Date:  1998-09-01       Impact factor: 11.361

8.  A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontia.

Authors:  Dolrudee Jumlongras; Jenn-Yih Lin; Anas Chapra; Christine E Seidman; Jonathan G Seidman; Richard L Maas; Bjorn R Olsen
Journal:  Hum Genet       Date:  2003-12-19       Impact factor: 4.132

9.  Pax-1, a regulator of sclerotome development is induced by notochord and floor plate signals in avian embryos.

Authors:  C Ebensperger; J Wilting; B Brand-Saberi; Y Mizutani; B Christ; R Balling; H Koseki
Journal:  Anat Embryol (Berl)       Date:  1995-04

10.  Lune/eye gone, a Pax-like protein, uses a partial paired domain and a homeodomain for DNA recognition.

Authors:  S Jun; R V Wallen; A Goriely; B Kalionis; C Desplan
Journal:  Proc Natl Acad Sci U S A       Date:  1998-11-10       Impact factor: 11.205

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