Literature DB >> 12399393

Hague (Hag). A new mouse hair mutation with an unstable semidominant allele.

Christophe Poirier1, Atsushi Yoshiki, Kyoko Fujiwara, Jean-Louis Guénet, Moriaki Kusakabe.   

Abstract

A spontaneous mouse hair mutation was identified in a C3H/HeN colony. The mode of inheritance of the mutation was semidominant, with incomplete penetrance when heterozygous. The trait is controlled by a single locus hague (Hag), which was mapped to the telomeric region of chromosome 15. This mutation was shown to be unstable, since its transmission could be switched from semidominant to recessive. To identify the causative gene and the nature of the mutation, hague was introduced into a high-resolution and high-density molecular genetic map. Over 2000 meioses were analyzed and the mutation was mapped to the keratin 2 complex genes. A YAC and BAC physical map of the critical region was then constructed and the gene involved was located in a 600- to 800-kb-long segment. Fourteen genes were mapped to this region; of these, 11 were expressed in the skin (5 epidermic cytokeratin and 6 hard keratin genes), but none were mutated in hague mice.

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Year:  2002        PMID: 12399393      PMCID: PMC1462301     

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  38 in total

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Authors:  S A Miller; D D Dykes; H F Polesky
Journal:  Nucleic Acids Res       Date:  1988-02-11       Impact factor: 16.971

2.  Label-retaining cells reside in the bulge area of pilosebaceous unit: implications for follicular stem cells, hair cycle, and skin carcinogenesis.

Authors:  G Cotsarelis; T T Sun; R M Lavker
Journal:  Cell       Date:  1990-06-29       Impact factor: 41.582

3.  Orthogonal-field-alternation gel electrophoresis.

Authors:  G F Carle; M V Olson
Journal:  Methods Enzymol       Date:  1987       Impact factor: 1.600

4.  Expression of MK6a dominant-negative and C-terminal mutant transgenes in mice has distinct phenotypic consequences in the epidermis and hair follicle.

Authors:  S M Wojcik; S Imakado; T Seki; M A Longley; L Petherbridge; D S Bundman; J R Bickenbach; J A Rothnagel; D R Roop
Journal:  Differentiation       Date:  1999-10       Impact factor: 3.880

5.  Mutant keratin expression in transgenic mice causes marked abnormalities resembling a human genetic skin disease.

Authors:  R Vassar; P A Coulombe; L Degenstein; K Albers; E Fuchs
Journal:  Cell       Date:  1991-01-25       Impact factor: 41.582

6.  Delayed wound healing in keratin 6a knockout mice.

Authors:  S M Wojcik; D S Bundman; D R Roop
Journal:  Mol Cell Biol       Date:  2000-07       Impact factor: 4.272

7.  Influence of maternal phenotype on metabolic differentiation of agouti locus mutants in the mouse.

Authors:  G L Wolff
Journal:  Genetics       Date:  1978-03       Impact factor: 4.562

8.  Organization of the human keratin type II gene cluster at 12q13.

Authors:  S J Yoon; J LeBlanc-Straceski; D Ward; K Krauter; R Kucherlapati
Journal:  Genomics       Date:  1994-12       Impact factor: 5.736

9.  Cyclic hair-loss and regrowth in transgenic mice overexpressing an intermediate filament gene.

Authors:  B C Powell; G E Rogers
Journal:  EMBO J       Date:  1990-05       Impact factor: 11.598

10.  Introducing a null mutation in the mouse K6alpha and K6beta genes reveals their essential structural role in the oral mucosa.

Authors:  P Wong; E Colucci-Guyon; K Takahashi; C Gu; C Babinet; P A Coulombe
Journal:  J Cell Biol       Date:  2000-08-21       Impact factor: 10.539

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Journal:  Mamm Genome       Date:  2010-10-16       Impact factor: 2.957

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Authors:  Yoshiaki Kikkawa; Ayumi Oyama; Rie Ishii; Ikuo Miura; Takashi Amano; Yoshiyuki Ishii; Yasuhiro Yoshikawa; Hiroshi Masuya; Shigeharu Wakana; Toshihiko Shiroishi; Choji Taya; Hiromichi Yonekawa
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3.  A novel hairless mouse model on an atopic dermatitis-prone genetic background generated by receptor-mediated transgenesis.

Authors:  Toyoyuki Takada; Hiroshi Shitara; Kunie Matsuoka; Erika Kojima; Rie Ishii; Yoshiaki Kikkawa; Choji Taya; Hajime Karasuyama; Kenji Kohno; Hiromichi Yonekawa
Journal:  Transgenic Res       Date:  2008-08-07       Impact factor: 2.788

4.  Neutral sphingomyelinase 2 deficiency is associated with lung anomalies similar to emphysema.

Authors:  Christophe Poirier; Evgeny V Berdyshev; Christiana Dimitropoulou; Natalia V Bogatcheva; Paul W Biddinger; Alexander D Verin
Journal:  Mamm Genome       Date:  2012-09-04       Impact factor: 2.957

5.  Dominant suppression of repeat-induced point mutation in Neurospora crassa by a variant catalytic subunit of DNA polymerase zeta.

Authors:  Ranjan Tamuli; Durgadas P Kasbekar
Journal:  Genetics       Date:  2008-02-03       Impact factor: 4.562

  5 in total

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