Abstract
A 1.95-kilobase cDNA clone was isolated by screening a size-selected lambda gt10 cDNA library prepared from an Epstein-Barr virus-transformed B-cell line, IB4, with the Epstein-Barr virus BamHI M fragment. Sequence analysis revealed that this clone contains about 75% of the BMRF1 and the complete BMRF2 open reading frames. The transcript is not spliced, and the polyadenylation signal at base pair 2641 of the BamHI M fragment is used. Northern blots (RNA blots) indicate that this polyadenylation signal is used for three overlapping mRNAs. The sizes of these transcripts are 3.5, 2.6, and 1.5 kilobases.
MeSH Terms
Antigens, Viral/genetics
Base Sequence
DNA/analysis
DNA Restriction Enzymes/pharmacology
Deoxyribonuclease BamHI
Epstein-Barr Virus Nuclear Antigens
Herpesvirus 4, Human/genetics
Poly A/metabolism
RNA/metabolism
RNA Splicing
RNA, Messenger/analysis
Transcription, Genetic
Chemicals
Antigens, Viral
Epstein-Barr Virus Nuclear Antigens
RNA, Messenger
Poly A
RNA
DNA
DNA Restriction Enzymes
Deoxyribonuclease BamHI
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Pfitzner A J
Strominger J L
Speck S H
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