Literature DB >> 8020960

Linkage mapping around the ragged (Ra) and wasted (wst) loci on distal mouse chromosome 2.

C Abbott1, S Malas, A Pilz, L Pate, R Ali, J Peters.   

Abstract

Mice that are heterozygous for the ragged (Ra) mutation, which is semidominant, have ragged coats caused by an absence of certain hair types. Ra/Ra homozygous mice usually die soon after birth, are naked, and have edema. Mice that are homozygous for the recessive mutation wasted (wst) appear normal until soon after weaning, but then develop tremors and ataxia, undergo atrophy of the thymus and spleen, and die by around 28 days of age. The Ra and wst loci map to distal mouse chromosome 2, but have never been positioned with respect to molecular markers. We have now mapped each of these genes in interspecific backcrosses that were also typed for available molecular markers. The results show that Ra maps very close to D2Mit74 and Acra-4, with no recombinants in 165 mice, whereas wst maps 3 cM distal to the most telomeric molecular marker on mouse chromosome 2, Acra-4.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 8020960     DOI: 10.1006/geno.1994.1131

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  7 in total

1.  The isolation and mapping of PCR markers specific to mouse Chromosome 2.

Authors:  S Malas; A Pilz; P A Lalley; L Pate; D A Stephenson; C Abbott
Journal:  Mamm Genome       Date:  1996-02       Impact factor: 2.957

2.  Localization of the rat stimulatory G-protein alpha subunit (GNPAS) gene to rat chromosome 3 by linkage analysis.

Authors:  N Kato; M Bihoreau; G M Lathrop; J P Rapp
Journal:  Mamm Genome       Date:  1996-08       Impact factor: 2.957

3.  Chromosome localization of two new mammalian kinases related to yeast and fly chromosome segregation-regulators.

Authors:  G Gopalan; D J Gilbert; N G Copeland; N A Jenkins; P J Donovan
Journal:  Mamm Genome       Date:  1998-01       Impact factor: 2.957

4.  The genes for endothelin 3, vitamin D 24-hydroxylase, and melanocortin 3 receptor map to distal mouse chromosome 2, in the region of conserved synteny with human chromosome 20.

Authors:  S Malas; J Peters; C Abbott
Journal:  Mamm Genome       Date:  1994-09       Impact factor: 2.957

5.  The lethal mutation of the mouse wasted (wst) is a deletion that abolishes expression of a tissue-specific isoform of translation elongation factor 1alpha, encoded by the Eef1a2 gene.

Authors:  D M Chambers; J Peters; C M Abbott
Journal:  Proc Natl Acad Sci U S A       Date:  1998-04-14       Impact factor: 11.205

6.  Genetic and physical mapping of the murine Sox1 gene.

Authors:  S Malas; M Sartor; S Duthie; K Hadjantonakis; R Lovell-Badge; V Episkopou
Journal:  Mamm Genome       Date:  1996-08       Impact factor: 2.957

7.  A high-resolution linkage map of the lethal spotting locus: a mouse model for Hirschsprung disease.

Authors:  W J Pavan; R A Liddell; A Wright; G Thibaudeau; P G Matteson; K M McHugh; L D Siracusa
Journal:  Mamm Genome       Date:  1995-01       Impact factor: 2.957

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.