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PMID: 9707621 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Consistent, persistent expression from modified retroviral vectors in murine hematopoietic stem cells.

Robbins PB, Skelton DC, Yu XJ, Halene S, Leonard EH, Kohn DB

Abstract

Retroviral vectors based on the Moloney murine leukemia virus (MoMuLV) have shown inconsistent levels and duration of expression as well as a propensity for the acquisition of de novo methylation in vivo. MoMuLV-based vectors are known to contain sequences that are capable of suppressing or preventing expression from the long terminal repeat. Previously, we constructed a series of modified retroviral vectors and showed that they function significantly better than MoMuLV-based vectors in vitro. To test the efficacy of the modified vectors in hematopoietic stem cells in vivo, we examined gene expression and proviral methylation in differentiated hematopoietic colonies formed in the spleens of mice after serial transplantation with transduced bone marrow (2 degreesCFU-S). We found a significant increase in the frequency of expression with our modified vectors (>90% expression in vector DNA containing 2 degreesCFU-S) over the frequency observed with the standard MoMuLV-based vector (28% expression in vector containing 2 degreesCFU-S). Expression from the modified vectors was highly consistent, with expression in >50% of the vector-containing 2 degreesCFU-S from all 20 transplant recipients analyzed, whereas expression from the standard MoMuLV-based vector was inconsistent, with expression in 0-10% of the vector containing 2 degreesCFU-S from 8 recipients and expression in >50% of the vector-containing 2 degreesCFU-S from 4 other recipients. In addition, we established that the modified vectors had a lower level of DNA methylation than the control vector. These findings represent significant advances in the development and evaluation of effective retroviral vectors for application in vivo.

MeSH Terms
Animals Base Sequence Bone Marrow Transplantation Colony-Forming Units Assay DNA Methylation DNA Primers/genetics DNA, Recombinant/genetics,metabolism Female Founder Effect Gene Expression Gene Transfer Techniques Genetic Vectors Hematopoietic Stem Cells/cytology,metabolism Male Mice Mice, Inbred C57BL Moloney murine leukemia virus/genetics Repetitive Sequences, Nucleic Acid Retroviridae/genetics Transduction, Genetic Transplantation, Isogeneic Virus Integration/genetics
Chemicals
DNA Primers DNA, Recombinant
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Robbins P B
Department of Molecular Microbiology and Immunology, Division of Research Immunology/Bone Marrow Transplantation, Childrens Hospital Los Angeles, University of Southern California School of Medicine, Los Angeles, CA 90027, USA.
Skelton D C
Yu X J
Halene S
Leonard E H
Kohn D B
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1998-08-18
Pages
10182-7
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC21482
Subset
IM
Grants
NCI NIH HHS · P01 CA059318 · United States
NCI NIH HHS · CA59318 · United States
NIDDK NIH HHS · DK4900 · United States
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