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PMID: 3369090 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Sequence variability and function of measles virus 3' and 5' ends and intercistronic regions.

Virology ·Vol. 164 ·No. 2 ·1988-06-00 ·Pages 498-506

Crowley JC, Dowling PC, Menonna J, Silverman JI, Schuback D, Cook SD, Blumberg BM

Abstract

Sequences critical for the activity of the measles virus (MV) RNA polymerase in transcription and replication were analyzed using a MV genomic cDNA library containing overlapping clones encompassing the entire MV genome. Clones corresponding to the 3' and 5' ends of the MV genome were identified and sequenced, and these sequences were confirmed by primer extension experiments. Neither (+) nor (-) strand leader RNAs were detected in MV-infected cell extracts, using high specific activity riboprobes made form these clones. Clones representing each of the MV gene boundaries were also sequenced, and variations including point mutations, insertions, and deletions were noted. Together with the sequence of the MV L gene region, this report completes the sequence determination of the MV genome.

MeSH Terms
Base Sequence Cloning, Molecular DNA/genetics Genes, Viral Genetic Variation Hydrogen Bonding Measles virus/genetics Molecular Sequence Data Nucleic Acid Conformation RNA, Viral/genetics
Chemicals
RNA, Viral DNA
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Crowley J C
Neurology Service, East Orange VA Medical Center, New Jersey 07019.
Dowling P C
Menonna J
Silverman J I
Schuback D
Cook S D
Blumberg B M
Article Info
Journal
Virology
Abbr.
Virology
ISSN
0042-6822
Published
1988-06-00
Pages
498-506
Language
English
Region
United States
NLM ID
0110674
Subset
IM
Databases
GENBANK
M20847, M20848, M20849, M20850
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