Literature DB >> 202671

Inverted complementary terminal sequences in single-stranded RNAs and snap-back RNAs from vesicular stomatitis defective interfering particles.

J Perrault, R W Leavitt.   

Abstract

Complementary single-stranded RNAs from three independent VSV defective interfering particle (DI) sources examined can anneal and give rise to monomeric and multimeric circular and linear double-stranded structures observable by electron microscopy under aqueous conditions. When the RNA from the shortest of these DI is spread from 80% formamide solutions, as many as 32% of the molecules are circular, suggesting that the single-stranded RNAs contain inverted complementary terminal sequences. This is strongly supported by the isolation of the putative terminal sequences which rapidly become RNase resistant base-paired structures after melting and quick-cooling the RNA. RNase digestion yields a major and a minor component, 60 to 70 and 135 to 170 nucleotides long respectively. Snap-back DI RNAs also contain inverted complementary sequences at both ends of the plus and minus strands of the duplexes since nicking these at the ends gives rise to double-stranded molecules which can form monomeric and multimeric circular and linear molecules. Thus, snap-back molecules most likely contain a covalent linkage between or near complementary terminal sequences on the two complementary strands as schematically shown in Fig. 5D.

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Year:  1978        PMID: 202671     DOI: 10.1099/0022-1317-38-1-35

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  33 in total

1.  UV inactivation of the biological activity of defective interfering particles generated by vesicular stomatitis virus.

Authors:  P H Bay; M E Reichmann
Journal:  J Virol       Date:  1979-12       Impact factor: 5.103

2.  Persistent vesicular stomatitis virus infection mediates base substitutions in viral RNA termini.

Authors:  B L Semler; J J Holland
Journal:  J Virol       Date:  1979-11       Impact factor: 5.103

3.  Synthesis of a small RNA in cells coinfected by standard and defective interfering particles of vesicular stomatitis virus.

Authors:  D D Rao; A S Huang
Journal:  Proc Natl Acad Sci U S A       Date:  1979-08       Impact factor: 11.205

4.  Sequence of a RNA templated by the 3'-OH RNA terminus of defective interfering particles of vesicular stomatitis virus.

Authors:  B L Semler; J Perrault; J Abelson; J J Holland
Journal:  Proc Natl Acad Sci U S A       Date:  1978-10       Impact factor: 11.205

5.  Structural analysis on the single-stranded genomic DNAs of the virus newly isolated from silkworm: the DNA molecules share a common terminal sequence.

Authors:  H Bando; H Choi; Y Ito; M Nakagaki; S Kawase
Journal:  Arch Virol       Date:  1992       Impact factor: 2.574

6.  Internal genome deletions in two distinct classes of defective interfering particles of vesicular stomatitis virus.

Authors:  J Perrault; B L Semler
Journal:  Proc Natl Acad Sci U S A       Date:  1979-12       Impact factor: 11.205

7.  Terminal sequences of vesicular stomatitis virus RNA are both complementary and conserved.

Authors:  J D Keene; M Schubert; R A Lazzarini
Journal:  J Virol       Date:  1979-10       Impact factor: 5.103

8.  Nucleotide sequence homology at the 3' termini of RNA from vesicular stomatitis virus and its defective interfering particles.

Authors:  J D Keene; M Schubert; R A Lazzarini; M Rosenberg
Journal:  Proc Natl Acad Sci U S A       Date:  1978-07       Impact factor: 11.205

9.  Sequence signal involved in the generation of an internally deleted defective interfering RNA from vesicular stomatitis virus.

Authors:  B K De; J Perrault
Journal:  Nucleic Acids Res       Date:  1982-11-11       Impact factor: 16.971

10.  Synthesis in vitro of the full-length complement of defective-interfering particle RNA of vesicular stomatitis virus.

Authors:  P K Chanda; C Y Kang; A K Banerjee
Journal:  Proc Natl Acad Sci U S A       Date:  1980-07       Impact factor: 11.205

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