Literature DB >> 18629032

Segmental trisomy of mouse chromosome 17: introducing an alternative model of Down's syndrome.

Jiri Forejt1, Tomás Vacík, Sona Gregorová.   

Abstract

All of the mouse models of human trisomy 21 syndrome that have been studied so far are based on segmental trisomies, encompassing, to a varying extent, distal chromosome 16. Their comparison with one or more unrelated and non-overlapping segmental trisomies may help to distinguish the effects of specific triplicated genes from the phenotypes caused by less specific developmental instability mechanisms. In this paper, the Ts43H segmental trisomy of mouse chromosome 17 is presented as such an alternative model. The trisomy stretches over 32.5 Mb of proximal chromosome 17 and includes 486 genes. The triplicated interval carries seven blocks of synteny with five human chromosomes. The block syntenic to human chromosome 21 contains 20 genes.

Entities:  

Year:  2003        PMID: 18629032      PMCID: PMC2447315          DOI: 10.1002/cfg.334

Source DB:  PubMed          Journal:  Comp Funct Genomics        ISSN: 1531-6912


  24 in total

Review 1.  The "gene dosage effect" hypothesis versus the "amplified developmental instability" hypothesis in Down syndrome.

Authors:  M A Pritchard; I Kola
Journal:  J Neural Transm Suppl       Date:  1999

Review 2.  Too much of a good thing: mechanisms of gene action in Down syndrome.

Authors:  R H Reeves; L L Baxter; J T Richtsmeier
Journal:  Trends Genet       Date:  2001-02       Impact factor: 11.639

Review 3.  A mouse phenome project.

Authors:  K Paigen; J T Eppig
Journal:  Mamm Genome       Date:  2000-09       Impact factor: 2.957

Review 4.  An answer to a complex problem: cloning the mouse t-complex responder.

Authors:  M F Lyon
Journal:  Mamm Genome       Date:  2000-10       Impact factor: 2.957

5.  Global up-regulation of chromosome 21 gene expression in the developing Down syndrome brain.

Authors:  Rong Mao; Carol L Zielke; H Ronald Zielke; Jonathan Pevsner
Journal:  Genomics       Date:  2003-05       Impact factor: 5.736

6.  Transcriptome analysis of human autosomal trisomy.

Authors:  David R FitzPatrick; Jacqueline Ramsay; Niolette I McGill; Mary Shade; Andrew D Carothers; Nicholas D Hastie
Journal:  Hum Mol Genet       Date:  2002-12-15       Impact factor: 6.150

7.  Overlapping deletions define novel embryonic lethal loci in the mouse t complex.

Authors:  Hanna H J Chao; Sarah E Mentzer; John C Schimenti; Yun You
Journal:  Genesis       Date:  2003-02       Impact factor: 2.487

Review 8.  Mouse autosomal trisomy: two's company, three's a crowd.

Authors:  D Hernandez; E M Fisher
Journal:  Trends Genet       Date:  1999-06       Impact factor: 11.639

Review 9.  Murine models for Down syndrome.

Authors:  M Dierssen; C Fillat; L Crnic; M Arbonés; J Flórez; X Estivill
Journal:  Physiol Behav       Date:  2001-08

10.  Discovery of imprinted transcripts in the mouse transcriptome using large-scale expression profiling.

Authors:  Itoshi Nikaido; Chika Saito; Yosuke Mizuno; Makiko Meguro; Hidemasa Bono; Moritoshi Kadomura; Tomohiro Kono; Gerard A Morris; Paul A Lyons; Mitsuo Oshimura; Yoshihide Hayashizaki; Yasushi Okazaki
Journal:  Genome Res       Date:  2003-06       Impact factor: 9.043

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  1 in total

1.  Segmental trisomy of chromosome 17: a mouse model of human aneuploidy syndromes.

Authors:  Tomás Vacík; Michael Ort; Sona Gregorová; Petr Strnad; Radek Blatny; Nathalie Conte; Allan Bradley; Jan Bures; Jirí Forejt
Journal:  Proc Natl Acad Sci U S A       Date:  2005-03-08       Impact factor: 11.205

  1 in total

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