Literature DB >> 8672134

Exclusion of Sox9 as a candidate for the mouse mutant tail-short.

K Uchida1, P Koopman, A Mita, S Wakana, E Wright, Y Kikkawa, H Yonekawa, K Moriwaki, T Shiroishi.   

Abstract

The Sry-related gene Sox9 has been proposed as the gene responsible for the mouse skeletal mutant Tail-short (Ts), on the basis of its expression in skeletogenic mesenchymal condensations in the mouse embryo and its chromosomal location in the region of Ts on distal Chromosome (Chr) 11. We present here detailed mapping of Ts locus relative to the Sox9, using an intersubspecific cross. Among 521 backcross progeny, 16 recombinants were detected between Sox9 and Ts, suggesting a separation of 3.5 +/- 0.01 cM, and excluding Sox9 as a candidate for Ts. A further nine recombinants were detected between Ts and the polycomb-like gene M33, suggesting that these loci are separated by 1.8 +/- 0.011 cM. Six microsatellite markers were co-localized to the Ts locus, providing reagents for positional cloning of Ts.

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Year:  1996        PMID: 8672134     DOI: 10.1007/s003359900147

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


  21 in total

1.  Abnormal development of the thoracic skeleton in mice homozygous for the gene for looped-tail.

Authors:  K F STEIN; J A MACKENSEN
Journal:  Am J Anat       Date:  1957-03

2.  Expression of a linear Sry transcript in the mouse genital ridge.

Authors:  Y W Jeske; J Bowles; A Greenfield; P Koopman
Journal:  Nat Genet       Date:  1995-08       Impact factor: 38.330

3.  The Nfe2l1 gene maps to distal mouse chromosome 11.

Authors:  J McKie; P J Scambler
Journal:  Mamm Genome       Date:  1996-01       Impact factor: 2.957

4.  Assignment of an autosomal sex reversal locus (SRA1) and campomelic dysplasia (CMPD1) to 17q24.3-q25.1.

Authors:  N Tommerup; W Schempp; P Meinecke; S Pedersen; L Bolund; C Brandt; C Goodpasture; P Guldberg; K R Held; H Reinwein
Journal:  Nat Genet       Date:  1993-06       Impact factor: 38.330

5.  In vivo and in vitro studies on the early embryonic lethal tail-short (Ts) in the mouse.

Authors:  H F Paterson
Journal:  J Exp Zool       Date:  1980-02

6.  Erythroid transcription factor NF-E2 is a haematopoietic-specific basic-leucine zipper protein.

Authors:  N C Andrews; H Erdjument-Bromage; M B Davidson; P Tempst; S H Orkin
Journal:  Nature       Date:  1993-04-22       Impact factor: 49.962

7.  Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene.

Authors:  J W Foster; M A Dominguez-Steglich; S Guioli; C Kwok; P A Weller; M Stevanović; J Weissenbach; S Mansour; I D Young; P N Goodfellow
Journal:  Nature       Date:  1994-12-08       Impact factor: 49.962

Review 8.  The campomelic syndrome: review, report of 17 cases, and follow-up on the currently 17-year-old boy first reported by Maroteaux et al in 1971.

Authors:  C S Houston; J M Opitz; J W Spranger; R I Macpherson; M H Reed; E F Gilbert; J Herrmann; A Schinzel
Journal:  Am J Med Genet       Date:  1983-05

9.  Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9.

Authors:  T Wagner; J Wirth; J Meyer; B Zabel; M Held; J Zimmer; J Pasantes; F D Bricarelli; J Keutel; E Hustert; U Wolf; N Tommerup; W Schempp; G Scherer
Journal:  Cell       Date:  1994-12-16       Impact factor: 41.582

10.  The mouse has a Polycomb-like chromobox gene.

Authors:  J J Pearce; P B Singh; S J Gaunt
Journal:  Development       Date:  1992-04       Impact factor: 6.868

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  2 in total

1.  Ectopic mineralization in the middle ear and chronic otitis media with effusion caused by RPL38 deficiency in the Tail-short (Ts) mouse.

Authors:  Konrad Noben-Trauth; Joseph R Latoche
Journal:  J Biol Chem       Date:  2010-11-09       Impact factor: 5.157

2.  Survival of Hoxa13 homozygous mutants reveals a novel role in digit patterning and appendicular skeletal development.

Authors:  Wilma D Perez; Crystal R Weller; Siming Shou; H Scott Stadler
Journal:  Dev Dyn       Date:  2010-02       Impact factor: 3.780

  2 in total

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