Literature DB >> 31445571

Research Techniques Made Simple: Forward Genetic Screening to Uncover Genes Involved in Skin Biology.

William McAlpine1, Jamie Russell1, Anne R Murray1, Bruce Beutler2, Emre Turer3.   

Abstract

The primary goals of modern genetics are to identify disease-causing mutations and to define the functions of genes in biological processes. Two complementary approaches, reverse and forward genetics, can be used to achieve this goal. Reverse genetics is a gene-driven approach that comprises specific gene targeting followed by phenotypic assessment. Conversely, forward genetics is a phenotype-driven approach that involves the phenotypic screening of organisms with randomly induced mutations followed by subsequent identification of the causative mutations (i.e., those responsible for phenotype). In this article, we focus on how forward genetics in mice can be used to explore dermatologic disease. We outline mouse mutagenesis with the chemical N-ethyl-N-nitrosourea and the strategy used to instantaneously identify mutations that are causative of specific phenotypes. Furthermore, we summarize the types of phenotypic screens that can be performed to explore various aspects of dermatologic disease.
Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved.

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Year:  2019        PMID: 31445571      PMCID: PMC6711397          DOI: 10.1016/j.jid.2019.04.013

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  17 in total

1.  Lanceolate hair-J (lahJ): a mouse model for human hair disorders.

Authors:  J P Sundberg; D Boggess; C Bascom; B J Limberg; L D Shultz; B A Sundberg; L E King; X Montagutelli
Journal:  Exp Dermatol       Date:  2000-06       Impact factor: 3.960

2.  Real-time resolution of point mutations that cause phenovariance in mice.

Authors:  Tao Wang; Xiaowei Zhan; Chun-Hui Bu; Stephen Lyon; David Pratt; Sara Hildebrand; Jin Huk Choi; Zhao Zhang; Ming Zeng; Kuan-wen Wang; Emre Turer; Zhe Chen; Duanwu Zhang; Tao Yue; Ying Wang; Hexin Shi; Jianhui Wang; Lei Sun; Jeff SoRelle; William McAlpine; Noelle Hutchins; Xiaoming Zhan; Maggy Fina; Rochelle Gobert; Jiexia Quan; McKensie Kreutzer; Stephanie Arnett; Kimberly Hawkins; Ashley Leach; Christopher Tate; Chad Daniel; Carlos Reyna; Lauren Prince; Sheila Davis; Joel Purrington; Rick Bearden; Jennifer Weatherly; Danielle White; Jamie Russell; Qihua Sun; Miao Tang; Xiaohong Li; Lindsay Scott; Eva Marie Y Moresco; Gerald M McInerney; Gunilla B Karlsson Hedestam; Yang Xie; Bruce Beutler
Journal:  Proc Natl Acad Sci U S A       Date:  2015-01-20       Impact factor: 11.205

Review 3.  The genetics of human skin disease.

Authors:  Gina M DeStefano; Angela M Christiano
Journal:  Cold Spring Harb Perspect Med       Date:  2014-10-01       Impact factor: 6.915

4.  The serine protease TMPRSS6 is required to sense iron deficiency.

Authors:  Xin Du; Ellen She; Terri Gelbart; Jaroslav Truksa; Pauline Lee; Yu Xia; Kevin Khovananth; Suzanne Mudd; Navjiwan Mann; Eva Marie Y Moresco; Ernest Beutler; Bruce Beutler
Journal:  Science       Date:  2008-05-01       Impact factor: 47.728

5.  Mice with mutations of Dock7 have generalized hypopigmentation and white-spotting but show normal neurological function.

Authors:  Amanda L Blasius; Katharina Brandl; Karine Crozat; Yu Xia; Kevin Khovananth; Philippe Krebs; Nora G Smart; Antonella Zampolli; Zaverio M Ruggeri; Bruce A Beutler
Journal:  Proc Natl Acad Sci U S A       Date:  2009-02-06       Impact factor: 11.205

6.  Enhanced sensitivity to DSS colitis caused by a hypomorphic Mbtps1 mutation disrupting the ATF6-driven unfolded protein response.

Authors:  Katharina Brandl; Sophie Rutschmann; Xiaohong Li; Xin Du; Nengming Xiao; Bernd Schnabl; David A Brenner; Bruce Beutler
Journal:  Proc Natl Acad Sci U S A       Date:  2009-02-06       Impact factor: 11.205

7.  A homozygous nonsense mutation in the gene for Tmem79, a component for the lamellar granule secretory system, produces spontaneous eczema in an experimental model of atopic dermatitis.

Authors:  Takashi Sasaki; Aiko Shiohama; Akiharu Kubo; Hiroshi Kawasaki; Akemi Ishida-Yamamoto; Taketo Yamada; Takayuki Hachiya; Atsushi Shimizu; Hideyuki Okano; Jun Kudoh; Masayuki Amagai
Journal:  J Allergy Clin Immunol       Date:  2013-09-20       Impact factor: 10.793

Review 8.  New insights into behaviour using mouse ENU mutagenesis.

Authors:  Peter L Oliver; Kay E Davies
Journal:  Hum Mol Genet       Date:  2012-08-13       Impact factor: 6.150

9.  Hypopigmentation and maternal-zygotic embryonic lethality caused by a hypomorphic mbtps1 mutation in mice.

Authors:  Sophie Rutschmann; Karine Crozat; Xiaohong Li; Xin Du; Jeffrey C Hanselman; Alana A Shigeoka; Katharina Brandl; Daniel L Popkin; Dianne B McKay; Yu Xia; Eva Marie Y Moresco; Bruce Beutler
Journal:  G3 (Bethesda)       Date:  2012-04-01       Impact factor: 3.154

10.  ENU-induced phenovariance in mice: inferences from 587 mutations.

Authors:  Carrie N Arnold; Michael J Barnes; Michael Berger; Amanda L Blasius; Katharina Brandl; Ben Croker; Karine Crozat; Xin Du; Celine Eidenschenk; Philippe Georgel; Kasper Hoebe; Hua Huang; Zhengfan Jiang; Philippe Krebs; Diantha La Vine; Xiaohong Li; Stephen Lyon; Eva Marie Y Moresco; Anne R Murray; Daniel L Popkin; Sophie Rutschmann; Owen M Siggs; Nora G Smart; Lei Sun; Koichi Tabeta; Victoria Webster; Wataru Tomisato; Sungyong Won; Yu Xia; Nengming Xiao; Bruce Beutler
Journal:  BMC Res Notes       Date:  2012-10-24
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