Characterization and location of myc homologous sequences in human cytomegalovirus DNA

E. P. Gelmann, D. J. Clanton, R. J. Jariwalla, L. J. Rosenthal

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

Specific DNA fragments from human cytomegalovirus (HCMV) strains Towne and AD169 exhibited homology to myc DNA sequences under hybridization conditions corresponding to a 22-28% base mismatch. In a specific subset of hybridizing HCMV fragments, the homology was restricted to the 5' half of viral v-myc and the 5' half of human c-myc. No hybridization was observed between HCMV fragments and the 3' v-myc and 3' human c-myc probes. In Towne DNA, myc homologous sequences mapped in four regions within the long unique segment (0.070-0.094, 0.134-0.156, 0.454-0.470, and 0.591-0.605 map unit) and one region in each of the short terminal repeats (0.832-0.847 and 0.984-1.0 map unit). In strain AD169, myc homology mapped in three regions within the long unique segment (0.123-0.147, 0.174-0.198, and 0.583-0.606 map unit) and one region in each of the short terminal repeats (0.833-0.863 and 0.976-1.0 map unit). By utilizing probes specific for the 5' and 3' portions of v-myc and human c-myc, we established that the regions of homology in a specific subset of HCMV restriction fragments corresponded to the 5' half of myc and were not due to MC29 viral helper sequences, flanking cellular sequences, or binding of probe to G-C-rich DNA.

Original languageEnglish (US)
Pages (from-to)5107-5111
Number of pages5
JournalProceedings of the National Academy of Sciences of the United States of America
Volume80
Issue number16 I
DOIs
StatePublished - 1983
Externally publishedYes

ASJC Scopus subject areas

  • General

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