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Journal of Virology, August 1999, p. 6946-6952, Vol. 73, No. 8
ABL-Basic Research Program, NCI-Frederick
Cancer Research and Development Center, Frederick, Maryland
21702-1201
Received 23 February 1999/Accepted 7 May 1999
RCASBP-M2C is a retroviral vector derived from an avian
sarcoma/leukosis virus which has been modified so that it uses the envelope gene from an amphotropic murine leukemia virus (E. V. Barsov and S. H. Hughes, J. Virol. 70:3922-3929, 1996). The
vector replicates efficiently in avian cells and infects, but does not replicate in, mammalian cells. This makes the vector useful for gene
delivery, mutagenesis, and other applications in mammalian systems.
Here we describe the development of a derivative of RCASBP-M2C, pGT-GFP, that can be used in gene trap experiments in mammalian cells.
The gene trap vector pGT-GFP contains a green fluorescent protein (GFP)
reporter gene. Appropriate insertion of the vector into genes causes
GFP expression; this facilitates the rapid enrichment and cloning of
the trapped cells and provides an opportunity to select subpopulations
of trapped cells based on the subcellular localization of GFP. With
this vector, we have generated about 90 gene-trapped lines using D17
and NIH 3T3 cells. Five trapped NIH 3T3 lines were selected based on
the distribution of GFP in cells. The cellular genes disrupted by viral
integration have been identified in four of these lines by using a 5'
rapid amplification of cDNA ends protocol.
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
An Avian Sarcoma/Leukosis Virus-Based Gene Trap
Vector for Mammalian Cells
*
Corresponding author. Mailing address: NCI-Frederick
Cancer Research and Development Center, P.O. Box B, Bldg. 539, Frederick, MD 21702-1201. Phone: (301) 846-1619. Fax: (301) 846-6966. E-mail: hughes{at}ncifcrf.gov.
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