Literature DB >> 199355

Further characterization of Sendai virus DI-RNAs: a model for their generation.

M Leppert, L Kort, D Kolakofsky.   

Abstract

Sendai virus DI-RNAs which contain complementary ends have been characterized as follows. First, the complementary ends of three DI-RNAs, although somewhat different in size (110-150 base pairs), contain sequences that are both identical to each other and to the 5' end of the nondefective (ND) genome. Second, almost all the sequences contained sequences that are both identical to each other and to the 5' end of the nondefective (ND) genome. Second, almost all the sequences contained in the DI-RNAs derive from sequences that are contiguous to the 5' end of the ND genome. The ND genome, on the other hand, does not contain any sequences that are complementary to its 5' end. A genetic map and a model for the generation of the Sendai DI-RNAs are presented.

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Year:  1977        PMID: 199355     DOI: 10.1016/0092-8674(77)90130-1

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  58 in total

1.  Complexes of Sendai virus NP-P and P-L proteins are required for defective interfering particle genome replication in vitro.

Authors:  S M Horikami; J Curran; D Kolakofsky; S A Moyer
Journal:  J Virol       Date:  1992-08       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.  Ends of the RNA within Sendai virus defective interfering nucleocapsids are not free.

Authors:  S Lynch; D Kolakofsky
Journal:  J Virol       Date:  1978-11       Impact factor: 5.103

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.  Ambisense gene expression from recombinant rabies virus: random packaging of positive- and negative-strand ribonucleoprotein complexes into rabies virions.

Authors:  S Finke; K K Conzelmann
Journal:  J Virol       Date:  1997-10       Impact factor: 5.103

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.  5'-triphosphate RNA requires base-paired structures to activate antiviral signaling via RIG-I.

Authors:  Andreas Schmidt; Tobias Schwerd; Wolfgang Hamm; Johannes C Hellmuth; Sheng Cui; Michael Wenzel; Franziska S Hoffmann; Marie-Cecile Michallet; Robert Besch; Karl-Peter Hopfner; Stefan Endres; Simon Rothenfusser
Journal:  Proc Natl Acad Sci U S A       Date:  2009-07-02       Impact factor: 11.205

9.  Template-switching during DNA synthesis by Thermus aquaticus DNA polymerase I.

Authors:  S J Odelberg; R B Weiss; A Hata; R White
Journal:  Nucleic Acids Res       Date:  1995-06-11       Impact factor: 16.971

10.  5' Terminus of defective and nondefective Sendai viral genomes is ppp Ap.

Authors:  M Leppert; D Kolakofsky
Journal:  J Virol       Date:  1978-01       Impact factor: 5.103

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