Literature DB >> 33948818

Wal Mutant Mice Have a Mutation Associated with Autism Spectrum Disorders.

E S Chermnykh1, D M Schepetov2, E A Vorotelyak2.   

Abstract

The waved alopecia (wal) mutation arose spontaneously in mice. Phenotypically, the wal mutation in a homozygous recessive state is manifested by a wavy coat. Over time, partial baldness develops, which leads to a thinning of the coat in mice. The molecular nature of the genetic defect in wal is still unknown; however, the coordinates of the chromosome locus in which the wal gene is located, a section of about 107 bp in length, has been determined in mouse chromosome 14. We examined the wal locus by sequencing the exons of candidate genes in which the mutation was expected, and performed genome-wide sequencing to identify the cause of the wal mutation. The sequences of exons of candidate genes located in this region did not carry changes that could lead to a change in the structure of the protein. However, outside the wal zone, a mutation in the Slc9a9 gene was found that is probably not associated with the wal phenotype. According to the literature, a mutation in the Slc9a9 gene leads to autism spectrum disorders. This is the first discovered spontaneous mutation in the Slc9a9 gene in mice.

Entities:  

Keywords:  Slc9a9; whole genome sequencing, mutant mice, autism spectrum disorders

Year:  2021        PMID: 33948818     DOI: 10.1134/S0012496621020010

Source DB:  PubMed          Journal:  Dokl Biol Sci        ISSN: 0012-4966


  7 in total

1.  SLC9A9 Co-expression modules in autism-associated brain regions.

Authors:  Jameson Patak; Jonathan L Hess; Yanli Zhang-James; Stephen J Glatt; Stephen V Faraone
Journal:  Autism Res       Date:  2016-07-21       Impact factor: 5.216

2.  Autism spectrum disorder traits in Slc9a9 knock-out mice.

Authors:  Lina Yang; Stephen V Faraone; Yanli Zhang-James
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2016-01-11       Impact factor: 3.568

3.  [The mutant gene "wal" is active in cells of mouse hair follicles].

Authors:  N A Malinina; M Iu Martynova; B V Koniukhov
Journal:  Ontogenez       Date:  1999 Sep-Oct

Review 4.  Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: annotated tables.

Authors:  M Nakamura; J P Sundberg; R Paus
Journal:  Exp Dermatol       Date:  2001-12       Impact factor: 3.960

5.  Targeted deletion of the sciellin gene resulted in normal development and maturation.

Authors:  Howard P Baden; Marie-France Champliaud; John P Sundberg; Alain Viel
Journal:  Genesis       Date:  2005-08       Impact factor: 2.487

6.  Characterization of sciellin, a precursor to the cornified envelope of human keratinocytes.

Authors:  J C Kvedar; M Manabe; S B Phillips; B S Ross; H P Baden
Journal:  Differentiation       Date:  1992-04       Impact factor: 3.880

7.  A mouse model of autism implicates endosome pH in the regulation of presynaptic calcium entry.

Authors:  Julie C Ullman; Jing Yang; Michael Sullivan; Jacob Bendor; Jonathan Levy; Ellen Pham; Katlin Silm; Helia Seifikar; Vikaas S Sohal; Roger A Nicoll; Robert H Edwards
Journal:  Nat Commun       Date:  2018-01-23       Impact factor: 14.919

  7 in total

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