Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:dateCreated
2005-7-12
pubmed:abstractText
The use of specialized reporter genes to monitor real-time, tissue-specific transgene expression in animal models offers an opportunity to circumvent current limitations associated with the establishment of transgenic mouse models. The Cre-loxP and the tetracycline (Tet)-inducible systems are useful methods of conditional gene expression that allow spatial (cell-type-specific) and temporal (inducer-dependent) control. Most often, the alpha-myosin heavy chain (alpha-MHC) promoter is used in these inducible systems to restrict expression of reporter genes and transgenes to the myocardium. An overview of each inducible system is described, along with suggested reporter genes for real-time, noninvasive imaging in the myocardium. Effective gene delivery of the inducible gene expression system is carried out by lentiviral vectors, which offer high transduction efficiency, long-term transgene expression, and low immunogenicity. This chapter outlines the packaging of myocardium-specific inducible expression systems into lentiviral vectors, in which a transgene and a reporter gene are transduced into cardiomyocytes. In doing so, transgene and reporter expression can be monitored/tracked with bioluminescence imaging (BLI) and positron emission tomography (PET).
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1543-1894
pubmed:author
pubmed:issnType
Print
pubmed:volume
112
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
109-54
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:16010014-Animals, pubmed-meshheading:16010014-Gene Expression Regulation, pubmed-meshheading:16010014-Gene Transfer Techniques, pubmed-meshheading:16010014-Genes, Reporter, pubmed-meshheading:16010014-Genetic Vectors, pubmed-meshheading:16010014-Green Fluorescent Proteins, pubmed-meshheading:16010014-Image Processing, Computer-Assisted, pubmed-meshheading:16010014-Integrases, pubmed-meshheading:16010014-Lac Operon, pubmed-meshheading:16010014-Lentivirus, pubmed-meshheading:16010014-Luciferases, pubmed-meshheading:16010014-Myocardium, pubmed-meshheading:16010014-Myocytes, Cardiac, pubmed-meshheading:16010014-Positron-Emission Tomography, pubmed-meshheading:16010014-Promoter Regions, Genetic, pubmed-meshheading:16010014-Recombinant Fusion Proteins, pubmed-meshheading:16010014-Recombination, Genetic, pubmed-meshheading:16010014-Repressor Proteins, pubmed-meshheading:16010014-Tetracycline, pubmed-meshheading:16010014-Thymidine Kinase, pubmed-meshheading:16010014-Transcriptional Activation, pubmed-meshheading:16010014-Transgenes, pubmed-meshheading:16010014-Viral Proteins
pubmed:year
2005
pubmed:articleTitle
Strategies of conditional gene expression in myocardium: an overview.
pubmed:affiliation
The James Hogg iCAPTURE Center for Cardiovascular and Pulmonary Research/MRL, University of British Columbia, St. Paul's Hospital, Vancouver, Canada.
pubmed:publicationType
Journal Article, Review, Research Support, Non-U.S. Gov't