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A collection of genetic mouse lines and related tools for inducible and reversible intersectional mis-expression.
Ahmadzadeh, Elham; Bayin, N Sumru; Qu, Xinli; Singh, Aditi; Madisen, Linda; Stephen, Daniel; Zeng, Hongkui; Joyner, Alexandra L; Rosello-Diez, Alberto.
Afiliação
  • Ahmadzadeh E; Australian Regenerative Medicine Institute, Monash University, Clayton, VIC 3800. Australia.
  • Bayin NS; Developmental Biology Program, Sloan Kettering Institute, New York, NY 10065, USA.
  • Qu X; Australian Regenerative Medicine Institute, Monash University, Clayton, VIC 3800. Australia.
  • Singh A; Australian Regenerative Medicine Institute, Monash University, Clayton, VIC 3800. Australia.
  • Madisen L; Allen Institute for Brain Science, Seattle, WA 98109, USA.
  • Stephen D; Developmental Biology Program, Sloan Kettering Institute, New York, NY 10065, USA.
  • Zeng H; Allen Institute for Brain Science, Seattle, WA 98109, USA.
  • Joyner AL; Developmental Biology Program, Sloan Kettering Institute, New York, NY 10065, USA alberto.rosellodiez@monash.edu joynera@mskcc.org.
  • Rosello-Diez A; Australian Regenerative Medicine Institute, Monash University, Clayton, VIC 3800. Australia alberto.rosellodiez@monash.edu joynera@mskcc.org.
Development ; 147(10)2020 05 28.
Article em En | MEDLINE | ID: mdl-32366677
ABSTRACT
Thanks to many advances in genetic manipulation, mouse models have become very powerful in their ability to interrogate biological processes. In order to precisely target expression of a gene of interest to particular cell types, intersectional genetic approaches using two promoter/enhancers unique to a cell type are ideal. Within these methodologies, variants that add temporal control of gene expression are the most powerful. We describe the development, validation and application of an intersectional approach that involves three transgenes, requiring the intersection of two promoter/enhancers to target gene expression to precise cell types. Furthermore, the approach uses available lines expressing tTA/rTA to control the timing of gene expression based on whether doxycycline is absent or present, respectively. We also show that the approach can be extended to other animal models, using chicken embryos. We generated three mouse lines targeted at the Tigre (Igs7) locus with TRE-loxP-tdTomato-loxP upstream of three genes (p21, DTA and Ctgf), and combined them with Cre and tTA/rtTA lines that target expression to the cerebellum and limbs. Our tools will facilitate unraveling biological questions in multiple fields and organisms.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Expressão Gênica / Regulação da Expressão Gênica / Técnicas de Transferência de Genes / Transgenes / Modelos Animais de Doenças Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Development Assunto da revista: BIOLOGIA / EMBRIOLOGIA Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Expressão Gênica / Regulação da Expressão Gênica / Técnicas de Transferência de Genes / Transgenes / Modelos Animais de Doenças Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Development Assunto da revista: BIOLOGIA / EMBRIOLOGIA Ano de publicação: 2020 Tipo de documento: Article