High rate of morphological reversion in tumor cell line H-19 associated with permanent transcriptional suppression of the LTR, v-src, LTR provirus
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.
Grant support
5R37-A128246-03
PHS HHS - United States
PubMed
8018560
Knihovny.cz E-resources
- MeSH
- Time Factors MeSH
- Transcription, Genetic * MeSH
- Genes, src * MeSH
- Virus Integration MeSH
- Cricetinae MeSH
- Mesocricetus MeSH
- Chickens MeSH
- Chick Embryo MeSH
- Molecular Sequence Data MeSH
- Mutation MeSH
- Proviruses genetics MeSH
- Repetitive Sequences, Nucleic Acid MeSH
- Base Sequence MeSH
- Suppression, Genetic * MeSH
- Cell Line, Transformed cytology microbiology MeSH
- Animals MeSH
- Check Tag
- Cricetinae MeSH
- Chick Embryo MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, U.S. Gov't, P.H.S. MeSH
The highly malignant line of morphologically transformed H-19 hamster tumor cells that harbor a single LTR, v-src, LTR provirus segregates morphologically flat revertants at the rate of 1.4 to 2.4 x 10(-3)/cell/cycle. Revertants behave like almost nonmalignant cells; they keep the provirus within an unaltered junction DNA fragment. However, the provirus is methylated, permanently transcriptionally silent, and not rescuable. Using the polymerase chain reaction, we have synthesized the whole proviral structure from two revertants and established that the left-hand long terminal repeats assuring transcription remained structurally intact. Moreover, the cloned proviral DNAs from three revertants were shown to produce tumors in chickens. The unusually high reversion rate together with the finding of structural integrity of proviral transcriptional signals in revertants indicate strongly that the reversion has been mediated by cell-regulatory mechanisms.
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