Literature DB >> 7812658

Cis-acting signals and trans-acting factors involved in influenza virus RNA synthesis.

R E O'Neill1, P Palese.   

Abstract

Influenza A virus RNA replication and expression is directed from cis-acting sequences present on the viral RNAs with the help of trans-acting factors encoded by the virus. Ribonucleoprotein (RNP) complexes reconstituted from synthetic cDNA-derived RNA and purified viral proteins have facilitated the dissection of these cis-acting signals and trans-acting factors. Prior to these studies influenza viruses and other negative-strand RNA viruses were refractory to molecular genetic manipulations. These reverse genetic studies have helped in defining the promoter and polyadenylation signals required for viral RNA synthesis. Studies involving the use of reconstituted RNP complexes have revealed that the viral proteins PB1, PB2, PA, and the nucleoprotein (NP) are necessary for replication and expression of influenza virus RNA. Inroads have also been made in determining the cellular proteins that participate in influenza virus gene expression and replication. The yeast interactive trap system has been used to identify and clone a gene (NPI-1), which encodes a protein that interacts with the influenza virus NP suggesting that this cellular protein is a trans-acting factor functioning in viral RNA synthesis.

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Year:  1994        PMID: 7812658

Source DB:  PubMed          Journal:  Infect Agents Dis        ISSN: 1056-2044


  9 in total

1.  Secondary structure determination of the conserved 98-base sequence at the 3' terminus of hepatitis C virus genome RNA.

Authors:  K J Blight; C M Rice
Journal:  J Virol       Date:  1997-10       Impact factor: 5.103

2.  A 68-nucleotide sequence within the 3' noncoding region of simian hemorrhagic fever virus negative-strand RNA binds to four MA104 cell proteins.

Authors:  Y K Hwang; M A Brinton
Journal:  J Virol       Date:  1998-05       Impact factor: 5.103

3.  Sequence and structural elements at the 3' terminus of bovine viral diarrhea virus genomic RNA: functional role during RNA replication.

Authors:  H Yu; C W Grassmann; S E Behrens
Journal:  J Virol       Date:  1999-05       Impact factor: 5.103

4.  Mov34 protein from mouse brain interacts with the 3' noncoding region of Japanese encephalitis virus.

Authors:  M Ta; S Vrati
Journal:  J Virol       Date:  2000-06       Impact factor: 5.103

5.  RNA-protein interactions: involvement of NS3, NS5, and 3' noncoding regions of Japanese encephalitis virus genomic RNA.

Authors:  C J Chen; M D Kuo; L J Chien; S L Hsu; Y M Wang; J H Lin
Journal:  J Virol       Date:  1997-05       Impact factor: 5.103

6.  Role of the 5'-proximal stem-loop structure of the 5' untranslated region in replication and translation of hepatitis C virus RNA.

Authors:  Guangxiang Luo; Shaojie Xin; Zhaohui Cai
Journal:  J Virol       Date:  2003-03       Impact factor: 5.103

7.  Translation elongation factor-1 alpha interacts with the 3' stem-loop region of West Nile virus genomic RNA.

Authors:  J L Blackwell; M A Brinton
Journal:  J Virol       Date:  1997-09       Impact factor: 5.103

8.  Identification of a highly conserved sequence element at the 3' terminus of hepatitis C virus genome RNA.

Authors:  A A Kolykhalov; S M Feinstone; C M Rice
Journal:  J Virol       Date:  1996-06       Impact factor: 5.103

9.  BHK cell proteins that bind to the 3' stem-loop structure of the West Nile virus genome RNA.

Authors:  J L Blackwell; M A Brinton
Journal:  J Virol       Date:  1995-09       Impact factor: 5.103

  9 in total

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