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PMID: 2225067 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Overexpression of TAR sequences renders cells resistant to human immunodeficiency virus replication.

Cell ·Vol. 63 ·No. 3 ·1990-11-02 ·Pages 601-8

Sullenger BA, Gallardo HF, Ungers GE, Gilboa E

Abstract

Overexpression of TAR-containing sequences (TAR decoys) was used to render cells resistant to HIV replication. A chimeric tRNA(meti)-TAR transcription unit contained in a double copy murine retroviral vector was used to express high levels of HIV-1 TAR-containing transcripts in CEM SS cells. Replication of HIV-1 was inhibited over 99% in cells expressing chimeric tRNA-TAR transcripts, but an amphotropic murine retrovirus replicated normally in these cells. Expression of TAR sequences in CEM SS cells had no adverse effects on cell viability, indicating that essential cellular factors are not being sequestered in these cells. TAR decoy RNA-mediated HIV inhibition may also be effective against natural HIV isolates in spite of their hypervariable nature, as suggested by the fact that replication of SIVmac was also inhibited in cells expressing HIV-1 TAR decoys.

MeSH Terms
Base Sequence Cell Line Genetic Vectors HIV Long Terminal Repeat/genetics HIV-1/genetics,physiology Humans Molecular Sequence Data Oligonucleotide Probes RNA, Transfer, Met/genetics RNA, Viral/genetics Transcription, Genetic Virus Replication
Chemicals
Oligonucleotide Probes RNA, Transfer, Met RNA, Viral
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Sullenger B A
Program of Molecular Biology, Memorial Sloan-Kettering Cancer Center, New York, New York 10021.
Gallardo H F
Ungers G E
Gilboa E
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1990-11-02
Pages
601-8
Language
English
Region
United States
NLM ID
0413066
Subset
IM
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