Literature DB >> 7402301

Binding of adenovirus VA RNA to mRNA: a possible role in splicing?

M B Mathews.   

Abstract

Most, though not all, of the messenger RNAs of higher cells are composed of transcripts from two or more non-contiguous DNA segments that are 'spliced' together by mechanisms which are poorly understood. There has been recent speculation that small RNA molecules may play a part in the splicing reaction, acting as templates or adaptors to stabilize the appropriate conformation of a precursor RNA. Adenovirus-2 codes for two low molecular weight RNAs, the virus-associate (VA) RNAs I and II, major and minor species, respectively. These RNAs are about 160 nucleotides long and have both been sequenced. They originate from closely spaced genes which are transcribed by RNA polymerase III, but have not been definitively associated with any function. We have shown previously that a fraction of the VA RNA of infected cells is complexed with high molecular weight RNA in a denaturation-sensitive fashion. Results presented here show that the VA RNAs bind to unfractionated late virus mRNA and to a cloned copy of a single mRNA species, but not to corresponding cloned segments of viral genomic DNA. It is suggested that VA RNA may act as a template in the splicing reaction.

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Year:  1980        PMID: 7402301     DOI: 10.1038/285575a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  33 in total

1.  Translation by the adenovirus tripartite leader: elements which determine independence from cap-binding protein complex.

Authors:  P J Dolph; J T Huang; R J Schneider
Journal:  J Virol       Date:  1990-06       Impact factor: 5.103

Review 2.  Adenovirus virus-associated RNA and translation control.

Authors:  M B Mathews; T Shenk
Journal:  J Virol       Date:  1991-11       Impact factor: 5.103

3.  Striking similarities are exhibited by two small Epstein-Barr virus-encoded ribonucleic acids and the adenovirus-associated ribonucleic acids VAI and VAII.

Authors:  M D Rosa; E Gottlieb; M R Lerner; J A Steitz
Journal:  Mol Cell Biol       Date:  1981-09       Impact factor: 4.272

4.  A model for the initiation of translation at the late stage after infection by adenoviruses.

Authors:  A Murasugi
Journal:  Biochem J       Date:  1989-06-01       Impact factor: 3.857

5.  The adenovirus L4 100-kilodalton protein is necessary for efficient translation of viral late mRNA species.

Authors:  B W Hayes; G C Telling; M M Myat; J F Williams; S J Flint
Journal:  J Virol       Date:  1990-06       Impact factor: 5.103

6.  Anti-sense regions in satellite RNA of cucumber mosaic virus form stable complexes with the viral coat protein gene.

Authors:  M A Rezaian; R H Symons
Journal:  Nucleic Acids Res       Date:  1986-04-25       Impact factor: 16.971

7.  A low-molecular-weight RNA from mouse ascites cells that hybridizes to both 18S rRNA and mRNA sequences.

Authors:  E S Maxwell; T E Martin
Journal:  Proc Natl Acad Sci U S A       Date:  1986-10       Impact factor: 11.205

8.  Nucleotide sequence complementarity between adenovirus 2-coded VA RNA and host cell pre-mRNA. A possible regulatory mechanism of cellular RNA splicing by VA RNA.

Authors:  H Naora; N J Deacon
Journal:  Mol Biol Rep       Date:  1981-05-22       Impact factor: 2.316

9.  mRNA in human cells contains sequences complementary to the Alu family of repeated DNA.

Authors:  B Calabretta; D L Robberson; A L Maizel; G F Saunders
Journal:  Proc Natl Acad Sci U S A       Date:  1981-10       Impact factor: 11.205

10.  Transcription of adenovirus cores in vitro: major RNA products differ from those made from a DNA template.

Authors:  E Daniell; M J Fedor
Journal:  Proc Natl Acad Sci U S A       Date:  1982-03       Impact factor: 11.205

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