Literature DB >> 11350121

Mutations of the mouse Twist and sy (fibrillin 2) genes induced by chemical mutagenesis of ES cells.

V L Browning1, S S Chaudhry, A Planchart, M J Dixon, J C Schimenti.   

Abstract

A prior phenotype-based screen of mice derived from ethylmethanesulfonate-mutagenized embryonic stem cells yielded two mouse limb defect mutants. Animals heterozygous for the polydactyly ems (Pde) mutation display preaxial polydactyly of the hindlimbs, and homozygous syndactyly ems (sne) animals are characterized by a fusion of the middle digits of their hindlimbs and sometimes forelimbs. We now report that Pde is a new allele of the basic helix-loop-helix protein gene Twist. Sequencing the full-length cDNA and several hundred basepairs of genomic DNA upstream of the coding region failed to reveal a mutation, suggesting that the lesion may be in a regulatory element of the gene. sne is a new fused phalanges (fp) allele of the shaker-with-syndactylism deletion complex (sy), and we show that the genomic lesion is a small deletion removing an entire exon, coincident with the insertion of the 3' end of a LINE element belonging to the TF subfamily. Copyright 2001 Academic Press.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11350121     DOI: 10.1006/geno.2001.6523

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  10 in total

1.  Genomewide two-generation screens for recessive mutations by ES cell mutagenesis.

Authors:  Robert J Munroe; Susan L Ackerman; John C Schimenti
Journal:  Mamm Genome       Date:  2004-12       Impact factor: 2.957

Review 2.  The molecular genetics of Marfan syndrome and related disorders.

Authors:  P N Robinson; E Arteaga-Solis; C Baldock; G Collod-Béroud; P Booms; A De Paepe; H C Dietz; G Guo; P A Handford; D P Judge; C M Kielty; B Loeys; D M Milewicz; A Ney; F Ramirez; D P Reinhardt; K Tiedemann; P Whiteman; M Godfrey
Journal:  J Med Genet       Date:  2006-03-29       Impact factor: 6.318

3.  Homozygous nonsense mutations in TWIST2 cause Setleis syndrome.

Authors:  Turgut Tukel; Drazen Šošić; Lihadh I Al-Gazali; Mónica Erazo; Jose Casasnovas; Hector L Franco; James A Richardson; Eric N Olson; Carmen L Cadilla; Robert J Desnick
Journal:  Am J Hum Genet       Date:  2010-08-13       Impact factor: 11.025

4.  ENU mutagenesis reveals a novel phenotype of reduced limb strength in mice lacking fibrillin 2.

Authors:  Gaynor Miller; Monica Neilan; Ruth Chia; Nabeia Gheryani; Natalie Holt; Annabelle Charbit; Sara Wells; Valter Tucci; Zuzanne Lalanne; Paul Denny; Elizabeth M C Fisher; Michael Cheeseman; Graham N Askew; T Neil Dear
Journal:  PLoS One       Date:  2010-02-09       Impact factor: 3.240

5.  A new mouse limb mutation identifies a Twist allele that requires interacting loci on chromosome 4 for its phenotypic expression.

Authors:  Isabelle Blanc; Antoine Bach; Yvan Lallemand; Fabienne Perrin-Schmitt; Jean-Louis Guénet; Benoît Robert
Journal:  Mamm Genome       Date:  2003-12       Impact factor: 2.957

6.  Evidence consistent with human L1 retrotransposition in maternal meiosis I.

Authors:  Brook Brouha; Christof Meischl; Eric Ostertag; Martin de Boer; Yue Zhang; Herman Neijens; Dirk Roos; Haig H Kazazian
Journal:  Am J Hum Genet       Date:  2002-07-01       Impact factor: 11.025

7.  Ocular phenotype of Fbn2-null mice.

Authors:  Yanrong Shi; Yidong Tu; Robert P Mecham; Steven Bassnett
Journal:  Invest Ophthalmol Vis Sci       Date:  2013-11-01       Impact factor: 4.799

8.  Efficient gene-driven germ-line point mutagenesis of C57BL/6J mice.

Authors:  Edward J Michaud; Cymbeline T Culiat; Mitchell L Klebig; Paul E Barker; K T Cain; Debra J Carpenter; Lori L Easter; Carmen M Foster; Alysyn W Gardner; Z Y Guo; Kay J Houser; Lori A Hughes; Marilyn K Kerley; Zhaowei Liu; Robert E Olszewski; Irina Pinn; Ginger D Shaw; Sarah G Shinpock; Ann M Wymore; Eugene M Rinchik; Dabney K Johnson
Journal:  BMC Genomics       Date:  2005-11-21       Impact factor: 3.969

9.  Optimizing Genomic Methods for Mapping and Identification of Candidate Variants in ENU Mutagenesis Screens Using Inbred Mice.

Authors:  Krista A Geister; Andrew E Timms; David R Beier
Journal:  G3 (Bethesda)       Date:  2018-02-02       Impact factor: 3.154

10.  Calvarial osteoblast gene expression in patients with craniosynostosis leads to novel polygenic mouse model.

Authors:  Jonas A Gustafson; Sarah S Park; Michael L Cunningham
Journal:  PLoS One       Date:  2019-08-23       Impact factor: 3.240

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.