Long terminal repeat enhancement of v-mos transforming activity: identification of essential regions
- PMID: 6190012
- PMCID: PMC256549
- DOI: 10.1128/JVI.46.3.726-736.1983
Long terminal repeat enhancement of v-mos transforming activity: identification of essential regions
Abstract
The transforming efficiency of recombinant DNA clones containing the Moloney sarcoma virus v-mos sequence was enhanced by introducing the Moloney sarcoma virus long terminal repeat (LTR) in either the 5' or 3' position relative to v-mos. We analyzed the polyadenylated RNA expressed in cells transformed by these recombinant DNA clones and examined the structural integrity of integrated copies of the DNA. In each case, we demonstrated the presence of v-mos containing RNA transcripts in the polyadenylated RNA and showed that these RNA transcripts are consistent with the structure of the transfected DNA. The analysis of DNA from these transformed cells showed that the relative positions of the v-mos and LTR sequences within the transfected DNA were conserved in the integrated DNA copies. These results demonstrate that a single LTR can successfully enhance the transforming activity of v-mos from either a 5' or a 3' relative position. The results from the transfection analysis of recombinant clones containing only portions of the LTR introduced 3' to v-mos demonstrate that the essential region of the LTR responsible for the enhancement of transformation is a region within the unique 3' sequences of the LTR containing the 73-base-pair tandem repeat sequence.
Similar articles
-
Sequences in the long terminal repeats of the Moloney murine sarcoma virus-124 genome which control transforming gene function.Virology. 1984 Aug;137(1):32-40. doi: 10.1016/0042-6822(84)90005-9. Virology. 1984. PMID: 6089418
-
Long terminal repeat sequences impart hematopoietic transformation properties to the myeloproliferative sarcoma virus.Proc Natl Acad Sci U S A. 1985 Sep;82(17):5746-50. doi: 10.1073/pnas.82.17.5746. Proc Natl Acad Sci U S A. 1985. PMID: 2994046 Free PMC article.
-
Use of the mouse mammary tumor virus long terminal repeat to promote steroid-inducible expression of v-mos.J Virol. 1984 Nov;52(2):420-30. doi: 10.1128/JVI.52.2.420-430.1984. J Virol. 1984. PMID: 6092668 Free PMC article.
-
Activation of the transforming potential of a normal cell sequence: a molecular model for oncogenesis.Science. 1981 May 22;212(4497):941-3. doi: 10.1126/science.7233190. Science. 1981. PMID: 7233190
-
Oncogenes--implications for human cancer: a review.J R Soc Med. 1984 May;77(5):410-6. doi: 10.1177/014107688407700515. J R Soc Med. 1984. PMID: 6374143 Free PMC article. Review. No abstract available.
Cited by
-
Retroviral endogenous transcripts related to the envelope gene of Friend spleen focus-forming virus in normal mouse tissues.Arch Virol. 1986;90(1-2):15-28. doi: 10.1007/BF01314141. Arch Virol. 1986. PMID: 2873806
-
Genetic analysis of myeloproliferative leukemia virus, a novel acute leukemogenic replication-defective retrovirus.J Virol. 1987 Feb;61(2):579-83. doi: 10.1128/JVI.61.2.579-583.1987. J Virol. 1987. PMID: 3027384 Free PMC article.
-
Lysine residue 121 in the proposed ATP-binding site of the v-mos protein is required for transformation.Proc Natl Acad Sci U S A. 1985 Dec;82(23):7894-8. doi: 10.1073/pnas.82.23.7894. Proc Natl Acad Sci U S A. 1985. PMID: 2999782 Free PMC article.
-
The human DNA polymerase beta gene structure. Evidence of alternative splicing in gene expression.Nucleic Acids Res. 1994 Jul 25;22(14):2719-25. doi: 10.1093/nar/22.14.2719. Nucleic Acids Res. 1994. PMID: 7914364 Free PMC article.
-
Characterization of enhancer elements in the long terminal repeat of Moloney murine sarcoma virus.J Virol. 1984 Jan;49(1):183-9. doi: 10.1128/JVI.49.1.183-189.1984. J Virol. 1984. PMID: 6690710 Free PMC article.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases