Literature DB >> 21195764

Cre recombinase resources for conditional mouse mutagenesis.

Damian Smedley1, Ekaterina Salimova, Nadia Rosenthal.   

Abstract

Large scale international activities for systematic conditional mouse mutagenesis, exploiting advances in the sophisticated manipulation of the mouse genome, has established the mouse as the premier organism for developing models of human disease and drug action. Conditional mutagenesis is critical for the elucidation of the gene functions that exert pleiotropic effects in a variety of cell types and tissues throughout the life of the animal. The majority of new mouse mutants are therefore designed as conditional, activated only in a specific tissue (spatial control) and/or life stage (temporal control) through biogenic Cre/loxP technologies. The full power of conditional mutant mice can therefore only be exploited with the availability of well characterized mouse lines expressing Cre-recombinase in tissue, organ and cell type-specific patterns, to allow the creation of somatic mutations in defined genes. This chapter provides an update on the current state of Cre driver mouse lines worldwide, and reviews the available public databases and portals that capture critical details of Cre driver lines such as the efficiency of recombination, cell tissue specificity, or genetic background effects. The continuously changing landscape of these mouse resources reflects the rapid progression of research and development in conditional and inducible mouse mutagenesis.
Copyright © 2011. Published by Elsevier Inc.

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Year:  2010        PMID: 21195764     DOI: 10.1016/j.ymeth.2010.12.027

Source DB:  PubMed          Journal:  Methods        ISSN: 1046-2023            Impact factor:   3.608


  20 in total

1.  Nkx2.2:Cre knock-in mouse line: a novel tool for pancreas- and CNS-specific gene deletion.

Authors:  Dina A Balderes; Mark A Magnuson; Lori Sussel
Journal:  Genesis       Date:  2013-10-01       Impact factor: 2.487

2.  Comparative analysis of the efficiency and specificity of myeloid-Cre deleting strains using ROSA-EYFP reporter mice.

Authors:  Clare L Abram; Gray L Roberge; Yongmei Hu; Clifford A Lowell
Journal:  J Immunol Methods       Date:  2014-05-22       Impact factor: 2.303

Review 3.  Mouse genetic and phenotypic resources for human genetics.

Authors:  Paul N Schofield; Robert Hoehndorf; Georgios V Gkoutos
Journal:  Hum Mutat       Date:  2012-05       Impact factor: 4.878

4.  The changing conditions of zebrafish mutants.

Authors:  Shawn M Burgess
Journal:  Proc Natl Acad Sci U S A       Date:  2012-09-04       Impact factor: 11.205

5.  Perinatal induction of Cre recombination with tamoxifen.

Authors:  Benoit Lizen; Melissa Claus; Lucie Jeannotte; Filippo M Rijli; Françoise Gofflot
Journal:  Transgenic Res       Date:  2015-09-22       Impact factor: 2.788

6.  A collection of genetic mouse lines and related tools for inducible and reversible intersectional mis-expression.

Authors:  Elham Ahmadzadeh; N Sumru Bayin; Xinli Qu; Aditi Singh; Linda Madisen; Daniel Stephen; Hongkui Zeng; Alexandra L Joyner; Alberto Rosello-Diez
Journal:  Development       Date:  2020-05-28       Impact factor: 6.868

Review 7.  Mouse resources for craniofacial research.

Authors:  Stephen A Murray
Journal:  Genesis       Date:  2011-04-01       Impact factor: 2.487

Review 8.  Mouse models for liver cancer.

Authors:  Latifa Bakiri; Erwin F Wagner
Journal:  Mol Oncol       Date:  2013-02-05       Impact factor: 6.603

Review 9.  New tricks for old dogmas: optogenetic and designer receptor insights for Parkinson's disease.

Authors:  Elena M Vazey; Gary Aston-Jones
Journal:  Brain Res       Date:  2013-01-18       Impact factor: 3.252

10.  Beyond knockouts: cre resources for conditional mutagenesis.

Authors:  Stephen A Murray; Janan T Eppig; Damian Smedley; Elizabeth M Simpson; Nadia Rosenthal
Journal:  Mamm Genome       Date:  2012-08-29       Impact factor: 2.957

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