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Article: Complete nucleotide sequence of an infectious clone of Friend spleen focus-forming provirus: gp55 is an envelope fusion glycoprotein

TitleComplete nucleotide sequence of an infectious clone of Friend spleen focus-forming provirus: gp55 is an envelope fusion glycoprotein
Authors
Issue Date1983
Citation
Proceedings of the National Academy of Sciences of the United States of America, 1983, v. 80, n. 16, p. 5037-5041 How to Cite?
AbstractThe Friend spleen focus-forming provirus is 6,296 base pairs (bp) in length. Compared to Moloney murine leukemia virus, it has undergone five major deletions, three substitutions, and a number of minor alterations. Otherwise, these viruses are about 90% homologous. A 16-bp palindrome is found in the region thought to be involved in packaging and dimerization of the RNA genome. Premature termination of translation of the gag polyprotein is attributed to a 13-bp deletion in the p12 region. A substitution of xenotropic env sequences was identified in the 5' region of the env gene; 150 nucleotides 3' to this substitution, a deletion of 585 bp removes the site where the normal env precursor protein is cleaved to form gp70 and p15(E), resulting in a fusion protein of M(r) 44,725. Due to these changes, the env product gp55 is expected to have a substantially different conformation on the cell surface compared to either a xenotropic or ecotropic gp70 protein, and may be responsible for the rapid erythroleukemic potential of spleen focus-forming virus.
Persistent Identifierhttp://hdl.handle.net/10722/292274
ISSN
2023 Impact Factor: 9.4
2023 SCImago Journal Rankings: 3.737
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorClark, S. P.-
dc.contributor.authorMak, T. W.-
dc.date.accessioned2020-11-17T14:56:07Z-
dc.date.available2020-11-17T14:56:07Z-
dc.date.issued1983-
dc.identifier.citationProceedings of the National Academy of Sciences of the United States of America, 1983, v. 80, n. 16, p. 5037-5041-
dc.identifier.issn0027-8424-
dc.identifier.urihttp://hdl.handle.net/10722/292274-
dc.description.abstractThe Friend spleen focus-forming provirus is 6,296 base pairs (bp) in length. Compared to Moloney murine leukemia virus, it has undergone five major deletions, three substitutions, and a number of minor alterations. Otherwise, these viruses are about 90% homologous. A 16-bp palindrome is found in the region thought to be involved in packaging and dimerization of the RNA genome. Premature termination of translation of the gag polyprotein is attributed to a 13-bp deletion in the p12 region. A substitution of xenotropic env sequences was identified in the 5' region of the env gene; 150 nucleotides 3' to this substitution, a deletion of 585 bp removes the site where the normal env precursor protein is cleaved to form gp70 and p15(E), resulting in a fusion protein of M(r) 44,725. Due to these changes, the env product gp55 is expected to have a substantially different conformation on the cell surface compared to either a xenotropic or ecotropic gp70 protein, and may be responsible for the rapid erythroleukemic potential of spleen focus-forming virus.-
dc.languageeng-
dc.relation.ispartofProceedings of the National Academy of Sciences of the United States of America-
dc.titleComplete nucleotide sequence of an infectious clone of Friend spleen focus-forming provirus: gp55 is an envelope fusion glycoprotein-
dc.typeArticle-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.1073/pnas.80.16.5037-
dc.identifier.pmid6576374-
dc.identifier.pmcidPMC384183-
dc.identifier.scopuseid_2-s2.0-0020579601-
dc.identifier.volume80-
dc.identifier.issue16-
dc.identifier.spage5037-
dc.identifier.epage5041-
dc.identifier.isiWOS:A1983RD40300035-
dc.identifier.issnl0027-8424-

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