Literature DB >> 21254096

Genotyping mdx, mdx3cv, and mdx4cv mice by primer competition polymerase chain reaction.

Jin-Hong Shin1, Chady H Hakim, Keqing Zhang, Dongsheng Duan.   

Abstract

mdx, mdx3cv, and mdx4cv mice are among the most commonly used models for the study of Duchenne muscular dystrophy. Their disease is caused by point mutations in the dystrophin gene. Despite widespread use of these models, genotyping has not always been straightforward. Current methods require multiple polymerase chain reactions (PCRs), post-PCR manipulations, and/or special equipment/reagents. Herein we report a simple, robust PCR genotyping method based on primer competition. This approach could also be applied in genotyping other point-mutation models.
Copyright © 2010 Wiley Periodicals, Inc.

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Year:  2010        PMID: 21254096      PMCID: PMC3051167          DOI: 10.1002/mus.21873

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  17 in total

1.  Preparation of PCR-quality mouse genomic DNA with hot sodium hydroxide and tris (HotSHOT).

Authors:  G E Truett; P Heeger; R L Mynatt; A A Truett; J A Walker; M L Warman
Journal:  Biotechniques       Date:  2000-07       Impact factor: 1.993

2.  Snapback SSCP analysis: engineered conformation changes for the rapid typing of known mutations.

Authors:  S D Wilton; K Honeyman; S Fletcher; N G Laing
Journal:  Hum Mutat       Date:  1998       Impact factor: 4.878

3.  Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice.

Authors:  V M Chapman; D R Miller; D Armstrong; C T Caskey
Journal:  Proc Natl Acad Sci U S A       Date:  1989-02       Impact factor: 11.205

4.  Sequencing protocols to genotype mdx, mdx(4cv), and mdx(5cv) mice.

Authors:  Glen B Banks; Ariana C Combs; Jeffrey S Chamberlain
Journal:  Muscle Nerve       Date:  2010-08       Impact factor: 3.217

5.  X chromosome-linked muscular dystrophy (mdx) in the mouse.

Authors:  G Bulfield; W G Siller; P A Wight; K J Moore
Journal:  Proc Natl Acad Sci U S A       Date:  1984-02       Impact factor: 11.205

6.  The molecular basis of muscular dystrophy in the mdx mouse: a point mutation.

Authors:  P Sicinski; Y Geng; A S Ryder-Cook; E A Barnard; M G Darlison; P J Barnard
Journal:  Science       Date:  1989-06-30       Impact factor: 47.728

7.  PCR analysis of dystrophin gene mutation and expression.

Authors:  J S Chamberlain; N J Farwell; J R Chamberlain; G A Cox; C T Caskey
Journal:  J Cell Biochem       Date:  1991-07       Impact factor: 4.429

8.  A novel and simple method for genotyping the mdx mouse using high-resolution melt polymerase chain reaction.

Authors:  Andrea L Trebbin; Andrew J Hoey
Journal:  Muscle Nerve       Date:  2009-05       Impact factor: 3.217

9.  DMD(mdx3Cv) and DMD(mdx4Cv) dystrophin mutations in mice: rapid polymerase chain reaction genotyping.

Authors:  Sonia H Pearson-White
Journal:  Neuromuscul Disord       Date:  2002-05       Impact factor: 4.296

10.  Submucosal gland development in the airway is controlled by lymphoid enhancer binding factor 1 (LEF1).

Authors:  D Duan; Y Yue; W Zhou; B Labed; T C Ritchie; R Grosschedl; J F Engelhardt
Journal:  Development       Date:  1999-10       Impact factor: 6.868

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  35 in total

1.  Alpha 7 integrin preserves the function of the extensor digitorum longus muscle in dystrophin-null mice.

Authors:  Chady H Hakim; Dean J Burkin; Dongsheng Duan
Journal:  J Appl Physiol (1985)       Date:  2013-08-29

2.  Mouse genotyping in an hour.

Authors:  Andrea L Reid; Matthew S Alexander
Journal:  Muscle Nerve       Date:  2020-03-25       Impact factor: 3.217

3.  A new method of genotyping MDX4CV mice by PCR-RFLP analysis.

Authors:  Elisia D Tichy; Foteini Mourkioti
Journal:  Muscle Nerve       Date:  2017-03-21       Impact factor: 3.217

4.  Optical polarization tractography revealed significant fiber disarray in skeletal muscles of a mouse model for Duchenne muscular dystrophy.

Authors:  Y Wang; K Zhang; N B Wasala; D Duan; G Yao
Journal:  Biomed Opt Express       Date:  2015-01-07       Impact factor: 3.732

5.  MicroRNA-486-dependent modulation of DOCK3/PTEN/AKT signaling pathways improves muscular dystrophy-associated symptoms.

Authors:  Matthew S Alexander; Juan Carlos Casar; Norio Motohashi; Natássia M Vieira; Iris Eisenberg; Jamie L Marshall; Molly J Gasperini; Angela Lek; Jennifer A Myers; Elicia A Estrella; Peter B Kang; Frederic Shapiro; Fedik Rahimov; Genri Kawahara; Jeffrey J Widrick; Louis M Kunkel
Journal:  J Clin Invest       Date:  2014-05-01       Impact factor: 14.808

6.  Cathepsin S Contributes to the Pathogenesis of Muscular Dystrophy in Mice.

Authors:  Andoria Tjondrokoesoemo; Tobias G Schips; Michelle A Sargent; Davy Vanhoutte; Onur Kanisicak; Vikram Prasad; Suh-Chin J Lin; Marjorie Maillet; Jeffery D Molkentin
Journal:  J Biol Chem       Date:  2016-03-10       Impact factor: 5.157

7.  Probing the Pathogenesis of Duchenne Muscular Dystrophy Using Mouse Models.

Authors:  Alexander Morrison-Nozik; Saptarsi M Haldar
Journal:  Methods Mol Biol       Date:  2018

8.  Sarcospan integration into laminin-binding adhesion complexes that ameliorate muscular dystrophy requires utrophin and α7 integrin.

Authors:  Jamie L Marshall; Jennifer Oh; Eric Chou; Joy A Lee; Johan Holmberg; Dean J Burkin; Rachelle H Crosbie-Watson
Journal:  Hum Mol Genet       Date:  2014-12-11       Impact factor: 6.150

9.  SERCA1 overexpression minimizes skeletal muscle damage in dystrophic mouse models.

Authors:  Davi A G Mázala; Stephen J P Pratt; Dapeng Chen; Jeffery D Molkentin; Richard M Lovering; Eva R Chin
Journal:  Am J Physiol Cell Physiol       Date:  2015-02-04       Impact factor: 4.249

10.  Fast skeletal myofibers of mdx mouse, model of Duchenne muscular dystrophy, express connexin hemichannels that lead to apoptosis.

Authors:  Luis A Cea; Carlos Puebla; Bruno A Cisterna; Rosalba Escamilla; Aníbal A Vargas; Marina Frank; Paloma Martínez-Montero; Carmen Prior; Jesús Molano; Isabel Esteban-Rodríguez; Ignacio Pascual; Pía Gallano; Gustavo Lorenzo; Héctor Pian; Luis C Barrio; Klaus Willecke; Juan C Sáez
Journal:  Cell Mol Life Sci       Date:  2016-01-23       Impact factor: 9.261

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