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PMID: 6300428 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Genomic and copy-back 3' termini in Sendai virus defective interfering RNA species.

Journal of virology ·Vol. 45 ·No. 2 ·1983-02-00 ·Pages 659-64

Re GG, Gupta KC, Kingsbury DW

Abstract

Direct sequencing of nine Sendai virus defective interfering RNA species revealed two kinds of 3'-terminal sequences. Six RNA species had 3' termini identical to the virus genome (negative strand), confirming that internal deletions are a frequent cause of Sendai virus defectiveness. The other three RNA species had 3'-terminal sequences identical to that described as the complement of the 5' terminus of the virus genome (R. A. Lazzarini, J. D. Keene, and M. Schubert, Cell 26:145-154, 1981), indicating that they are of the copy-back type. Extensive homology between these two types of 3' sequences evidently accounts for the ability of the copy-back sequence to function as an initiation signal for viral RNA replication. There may not be a selective advantage of one type of terminus over the other, since one defective interfering strain possessed two RNA species, one of which had the genomic 3' terminus and the other copy-back type.

MeSH Terms
Base Sequence Defective Viruses/genetics Genes, Viral Parainfluenza Virus 1, Human/genetics RNA, Viral/genetics Virus Replication
Chemicals
RNA, Viral
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Re G G
Gupta K C
Kingsbury D W
References (17)
17 references, click to expand
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Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
1983-02-00
Pages
659-64
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC256460
Subset
IM
Grants
NIAID NIH HHS · AI05343 · United States
NCI NIH HHS · CA21765 · United States
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