Literature DB >> 9021139

A high-resolution genetic map around waltzer on mouse chromosome 10 and identification of a new allele of waltzer.

E C Bryda1, H Ling, L Flaherty.   

Abstract

A new autosomal recessive mouse mutation characterized by deafness and circling behavior was recovered during mutagenesis experiments with chlorambucil (CHL). On the basis of allelism tests and linkage analyses, this mutation appears to represent a new allele of waltzer (v) that maps to mouse Chromosome (Chr) 10. We have designated this new allele, Albany waltzer (vAlb). A high-resolution map of the region around v was constructed from data from two intersubspecific backcrosses involving Mus musculus castaneus. The analysis of 648 backcross mice has allowed vAlb to be localized 1.1 +/- 0.4 cM distal to D10Mit60 and 0.2 +/- 0.2 cM proximal to a cluster of four markers, D10Mit172, D10Mit112, D10Mit48, and D10Mit196. An independent backcross was used to confirm the map order and distances in the vAlb backcross. The two linkage maps were consistent, indicating that the lesion in vAlb, which is presumed to be a deletion based on the known action of CHL, is small and has not significantly altered the map at this level of detection. Additionally, three genes (Ros1, Grik2, and Zfa) were eliminated as possible candidates for vAlb, and several SSLP markers were separated genetically.

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Year:  1997        PMID: 9021139     DOI: 10.1007/s003359900336

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


  23 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

2.  The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse.

Authors:  M S DEOL
Journal:  Proc R Soc Lond B Biol Sci       Date:  1956-05-29

3.  Simplified mammalian DNA isolation procedure.

Authors:  P W Laird; A Zijderveld; K Linders; M A Rudnicki; R Jaenisch; A Berns
Journal:  Nucleic Acids Res       Date:  1991-08-11       Impact factor: 16.971

4.  Genetic and molecular analysis of chlorambucil-induced germ-line mutations in the mouse.

Authors:  E M Rinchik; J W Bangham; P R Hunsicker; N L Cacheiro; B S Kwon; I J Jackson; L B Russell
Journal:  Proc Natl Acad Sci U S A       Date:  1990-02       Impact factor: 11.205

5.  A one-hour procedure for the preparation of genomic DNA from frozen tissues.

Authors:  P Chapdelaine; S Delahaye; E Gauthier; R R Tremblay; J Y Dubé
Journal:  Biotechniques       Date:  1993-02       Impact factor: 1.993

6.  Rapid method for recovery of DNA from agarose gels.

Authors:  Z Lu; M Templer; B L Nielsen
Journal:  Biotechniques       Date:  1994-03       Impact factor: 1.993

7.  A comprehensive genetic map of the mouse genome.

Authors:  W F Dietrich; J Miller; R Steen; M A Merchant; D Damron-Boles; Z Husain; R Dredge; M J Daly; K A Ingalls; T J O'Connor
Journal:  Nature       Date:  1996-03-14       Impact factor: 49.962

8.  Defective myosin VIIA gene responsible for Usher syndrome type 1B.

Authors:  D Weil; S Blanchard; J Kaplan; P Guilford; F Gibson; J Walsh; P Mburu; A Varela; J Levilliers; M D Weston
Journal:  Nature       Date:  1995-03-02       Impact factor: 49.962

9.  The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells.

Authors:  K B Avraham; T Hasson; K P Steel; D M Kingsley; L B Russell; M S Mooseker; N G Copeland; N A Jenkins
Journal:  Nat Genet       Date:  1995-12       Impact factor: 38.330

10.  H beta 58, an insertional mutation affecting early postimplantation development of the mouse embryo.

Authors:  G Radice; J J Lee; F Costantini
Journal:  Development       Date:  1991-03       Impact factor: 6.868

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  5 in total

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Authors:  J M Bork; L M Peters; S Riazuddin; S L Bernstein; Z M Ahmed; S L Ness; R Polomeno; A Ramesh; M Schloss; C R Srisailpathy; S Wayne; S Bellman; D Desmukh; Z Ahmed; S N Khan; V M Kaloustian; X C Li; A Lalwani; S Riazuddin; M Bitner-Glindzicz; W E Nance; X Z Liu; G Wistow; R J Smith; A J Griffith; E R Wilcox; T B Friedman; R J Morell
Journal:  Am J Hum Genet       Date:  2000-11-21       Impact factor: 11.025

2.  Hearing loss associated with the modifier of deaf waddler (mdfw) locus corresponds with age-related hearing loss in 12 inbred strains of mice.

Authors:  Q Y Zheng; K R Johnson
Journal:  Hear Res       Date:  2001-04       Impact factor: 3.208

3.  A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice.

Authors:  K R Johnson; Q Y Zheng; Y Bykhovskaya; O Spirina; N Fischel-Ghodsian
Journal:  Nat Genet       Date:  2001-02       Impact factor: 38.330

4.  A new mouse mutant of the Cdh23 gene with early-onset hearing loss facilitates evaluation of otoprotection drugs.

Authors:  F Han; H Yu; C Tian; H E Chen; C Benedict-Alderfer; Y Zheng; Q Wang; X Han; Q Y Zheng
Journal:  Pharmacogenomics J       Date:  2010-07-20       Impact factor: 3.550

5.  The sound of silence: mouse models for hearing loss.

Authors:  Sumantra Chatterjee; Thomas Lufkin
Journal:  Genet Res Int       Date:  2011-10-09
  5 in total

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