Literature DB >> 15781974

Gene-targeting technologies for the study of neurological disorders.

Vassilios Beglopoulos1, Jie Shen.   

Abstract

Studies using genetic manipulations have proven invaluable in the research of neurological disorders. In the forefront of these approaches is the knockout technology that engineers a targeted gene mutation in mice resulting in inactivation of gene expression. In many cases, important roles of a particular gene in embryonic development have precluded the in vivo study of its function in the adult brain, which is usually the most relevant experimental context for the study of neurological disorders. The conditional knockout technology has provided a tool to overcome this restriction and has been used successfully to generate viable mouse models with gene inactivation patterns in certain regions or cell types of the postnatal brain. This review first describes the methodology of gene targeting in mice, detailing the aspects of designing a targeting vector, introducing it into embryonic stem cells in culture and screening for correct recombination events, and generating chimeric and null mutant mice from the positive clones. It then discusses the special issues and considerations for the generation of conditional knockout mice, including a section about approaches for inducible gene inactivation in the brain and some of their applications. An overview of gene-targeted mouse models that have been used in the study of several neurological disorders, including Alzheimer's disease, Parkinson's disease, Huntington's disease, seizure disorders, and schizophrenia, is also presented. The importance of the results obtained by these models for the understanding of the pathogenic mechanism underlying the disorders is discussed.

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Year:  2004        PMID: 15781974     DOI: 10.1385/NMM:6:1:013

Source DB:  PubMed          Journal:  Neuromolecular Med        ISSN: 1535-1084            Impact factor:   3.843


  84 in total

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Journal:  Nat Rev Genet       Date:  2001-10       Impact factor: 53.242

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Authors:  J O McNamara
Journal:  Nature       Date:  1999-06-24       Impact factor: 49.962

5.  Insoluble detergent-resistant aggregates form between pathological and nonpathological lengths of polyglutamine in mammalian cells.

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Journal:  Proc Natl Acad Sci U S A       Date:  1999-09-28       Impact factor: 11.205

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Authors:  David C Rubinsztein
Journal:  Trends Genet       Date:  2002-04       Impact factor: 11.639

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Journal:  Nature       Date:  1998-10-15       Impact factor: 49.962

8.  Ligand-activated site-specific recombination in mice.

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Journal:  Proc Natl Acad Sci U S A       Date:  1996-10-01       Impact factor: 11.205

9.  Gene replacement of the p53 gene with the lacZ gene in mouse embryonic stem cells and mice by using two steps of homologous recombination.

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Journal:  Biochem Biophys Res Commun       Date:  1994-07-29       Impact factor: 3.575

10.  Loss of huntingtin-mediated BDNF gene transcription in Huntington's disease.

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Journal:  Science       Date:  2001-06-14       Impact factor: 47.728

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  9 in total

Review 1.  Monoamine oxidases in development.

Authors:  Chi Chiu Wang; Ellen Billett; Astrid Borchert; Hartmut Kuhn; Christoph Ufer
Journal:  Cell Mol Life Sci       Date:  2012-07-11       Impact factor: 9.261

2.  Impaired neurotransmitter release in Alzheimer's and Parkinson's diseases.

Authors:  Jie Shen
Journal:  Neurodegener Dis       Date:  2010-02-18       Impact factor: 2.977

Review 3.  Schizophrenia: an integrative approach to modelling a complex disorder.

Authors:  George S Robertson; Sarah E Hori; Kelly J Powell
Journal:  J Psychiatry Neurosci       Date:  2006-05       Impact factor: 6.186

4.  Monoamine oxidase a expression is vital for embryonic brain development by modulating developmental apoptosis.

Authors:  Chi Chiu Wang; Astrid Borchert; Aslihan Ugun-Klusek; Ling Yin Tang; Wai Ting Lui; Ching Yan Chu; Ellen Billett; Hartmut Kuhn; Christoph Ufer
Journal:  J Biol Chem       Date:  2011-06-22       Impact factor: 5.157

5.  RFamide-Related Peptide Neurons Modulate Reproductive Function and Stress Responses.

Authors:  Asha Mamgain; India L Sawyer; David A M Timajo; Mohammed Z Rizwan; Maggie C Evans; Caroline M Ancel; Megan A Inglis; Greg M Anderson
Journal:  J Neurosci       Date:  2020-11-20       Impact factor: 6.167

6.  Mouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments.

Authors:  Mark R Etherton; Cory A Blaiss; Craig M Powell; Thomas C Südhof
Journal:  Proc Natl Acad Sci U S A       Date:  2009-10-12       Impact factor: 11.205

Review 7.  Function and dysfunction of presenilin.

Authors:  Jie Shen
Journal:  Neurodegener Dis       Date:  2013-10-02       Impact factor: 2.977

8.  Changes in the expression of genes associated with intraneuronal amyloid-beta and tau in Alzheimer's disease.

Authors:  Robert K Fujimura; Teresita Reiner; Fangchao Ma; Virginia Phillips; Alicia de las Pozas; Dennis W Dickson; Bernard A Roos; Guy A Howard; Carlos Perez-Stable
Journal:  J Alzheimers Dis       Date:  2010       Impact factor: 4.472

9.  Choroid plexus transport: gene deletion studies.

Authors:  Richard F Keep; David E Smith
Journal:  Fluids Barriers CNS       Date:  2011-11-04
  9 in total

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