Abstract
In the mouse myeloma XRPC-24 the DNA of an intracisternal A-particle (IAP) is inserted within the coding region of c-mos. This insertion splits the c-mos into a 3' rc-mos and a 5' rc-mos separated by approximately 4.7 kb of IAP DNA. The insertion is in a head-to-head orientation and brings the 5' LTR of the IAP in juxtaposition to the 3' rc-mos such that the IAP and the 3' rc-mos are transcribed in opposite directions. The intact c-mos gene is usually dormant, whereas the 3' rc-mos is actively transcribed and is capable of transforming NIH3T3 cells. In an effort to understand the nature of this activation we mapped the 5' ends of the 3' rc-mos mRNA present in XPRC-24. We found two main mRNA start sites, one mapping to the junction of the 3' rc-mos and the 5' LTR, and the other located 10 nucleotides upstream to this junction, within the 5' LTR. This result indicates that the 3' rc-mos in XRPC-24 was activated by insertion of a promoter provided by the LTR of an IAP genome. Furthermore, the 5' LTR appears to possess promoter activities in two directions. This conclusion was confirmed by the fact that this 5' LTR, in both orientations, was able to activate the bacterial gene coding for chloramphenicol acetyltransferase (CAT) in the modular vector pSVOCAT.
MeSH Terms
Acetyltransferases/genetics
Animals
Cell Line
Cell Transformation, Neoplastic
Cells, Cultured
Chloramphenicol O-Acetyltransferase
Chlorocebus aethiops
Cloning, Molecular
DNA Restriction Enzymes
DNA Transposable Elements
Genes
Kidney
Kinetics
Mice
Mice, Inbred Strains
Nucleic Acid Hybridization
Oncogenes
Plasmacytoma/genetics
Plasmids
Chemicals
DNA Transposable Elements
Acetyltransferases
Chloramphenicol O-Acetyltransferase
DNA Restriction Enzymes
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Horowitz M
Luria S
Rechavi G
Givol D
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