Abstract
cDNA prepared from the single-stranded circular RNA genome of hepatitis delta virus was cloned in lambda gt11 by using RNA from the liver of an infected woodchuck. From the sequence of overlapping clones, we assembled the full sequence of 1,679 nucleotides. The sequence indicated an exceptional ability for intramolecular base pairing, yielding a rod structure with at least 70% of the bases paired and a predicted free energy of -805 kcal (-3,368 kJ)/mol. Three of the lambda clones contained sequences that were not only expressed as fusion proteins with beta-galactosidase but were recognized by human hepatitis delta virus-specific antibody. These clones were sequenced so as to establish the reading frame of the delta antigen on the antigenomic strand. The fusion protein produced by one clone was purified by immunoaffinity chromatography and then was used to raise rabbit antibodies specific for the delta antigen.
MeSH Terms
Animals
Antigens, Viral/genetics,immunology
Base Sequence
Cloning, Molecular
DNA/genetics
Genes
Genes, Viral
Hepatitis Delta Virus/genetics,immunology
Hydrogen Bonding
Liver/microbiology
Marmota
Molecular Sequence Data
RNA, Viral/genetics
Recombinant Fusion Proteins/immunology
Viral Proteins/genetics
Chemicals
Antigens, Viral
RNA, Viral
Recombinant Fusion Proteins
Viral Proteins
DNA
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Kuo M Y
Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111.
Goldberg J
Coates L
Mason W
Gerin J
Taylor J
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