Literature DB >> 7031064

A unique class of compound, guanosine-nucleoside tetraphosphate G(5')pppp(5')N, synthesized during the in vitro transcription of cytoplasmic polyhedrosis virus of Bombyx mori. Structural determination and mechanism of formation.

R E Smith, Y Furuichi.   

Abstract

Two structurally different classes of oligonucleotides accumulate in vitro in cytoplasmic polyhedrosis virus (CPV) transcription mixtures in molar excess as compared to the completed RNA products. The first class consists of oligonucleotides which correspond to the 5'-terminal sequence of the virus mRNAs (referred to as initiator oligonucleotides). The major species of initiator oligonucleotides are (p)ppApG and (p)ppApGpN together with smaller amounts of homologous capped structures (Furuichi, Y. (1981) J. Biol. Chem. 256, 483-493). In addition to initiator oligonucleotides, CPV transcription mixtures yielded a second new class of compounds which were radiolabeled by [alpha-32P]GTP and resistant to phosphatase digestion. Their structures were identified as G(5')pppp(5')A, G(5')pppp(5')C, G(5')pppp(5')G, and G(5')pppp(5')U. With the exception of G(5')pppp(5')G, these compounds have not been observed previously. The mechanism of synthesis of these unique compounds was elucidated as pppG + pppN leads to GppppN + PPi. The reaction resembles, in principle, a guanylylation reaction which occurs during cap formation in CPV and other eukaryotic mRNA syntheses. It is likely that these compounds are formed in a similar way by a condensation reaction involving a viral guanylyltransferase-pG intermediate complex and ribonucleoside triphosphate. When the amounts of G(5')pppp(5')N were measured, it was found that G(5')pppp(5')N reached maximum concentrations (0.4 to 0.7 microM) shortly after the onset of RNA synthesis (1 h) and these levels were maintained or diminished gradually. By contrast, mRNA and (p)ppApG were continuously synthesized. The relative molar ratios of total G(5')pppp(5')N and (p)ppApG versus mRNA were comparable (74:24:1 and 30:27:1 during 1 to 4 h transcription, respectively). The results imply that these unusual compounds G(5')pppp(5')N as well as initiator oligonucleotides may be produced reiteratively during initiation when RNA chain elongation and capping are uncoupled.

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Year:  1982        PMID: 7031064

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  11 in total

Review 1.  An unconventional pathway of mRNA cap formation by vesiculoviruses.

Authors:  Tomoaki Ogino; Amiya K Banerjee
Journal:  Virus Res       Date:  2011-09-16       Impact factor: 3.303

2.  Reovirus guanylyltransferase is L2 gene product lambda 2.

Authors:  D R Cleveland; H Zarbl; S Millward
Journal:  J Virol       Date:  1986-10       Impact factor: 5.103

3.  Assay of adenosine 5'-P1-tetraphospho-P4-5"'-adenosine and adenosine 5'-P1-tetraphospho-P4-5"'-guanosine in Physarum polycephalum and other eukaryotes. An isocratic high-pressure liquid-chromatography method.

Authors:  P N Garrison; L D Barnes
Journal:  Biochem J       Date:  1984-02-01       Impact factor: 3.857

4.  Priming of reovirus transcription by GppppG and formation of CpG(5')GpC.

Authors:  M Yamakawa; Y Furuichi; A J Shatkin
Journal:  Proc Natl Acad Sci U S A       Date:  1982-10       Impact factor: 11.205

5.  Transcriptional regulation of three double-stranded RNA segments of bacteriophage phi 6 in vitro.

Authors:  Y Emori; H Iba; Y Okada
Journal:  J Virol       Date:  1983-04       Impact factor: 5.103

6.  Mutational analysis of the RNA triphosphatase component of vaccinia virus mRNA capping enzyme.

Authors:  L Yu; S Shuman
Journal:  J Virol       Date:  1996-09       Impact factor: 5.103

7.  Synthesis of Gp4N and Gp3N compounds by guanylyltransferase purified from yeast.

Authors:  D Wang; A J Shatkin
Journal:  Nucleic Acids Res       Date:  1984-03-12       Impact factor: 16.971

8.  Reaction mechanism of mRNA guanylyltransferase from rat liver: isolation and characterization of a guanylyl-enzyme intermediate.

Authors:  K Mizumoto; Y Kaziro; F Lipmann
Journal:  Proc Natl Acad Sci U S A       Date:  1982-03       Impact factor: 11.205

9.  Formation of guanosine(5')tetraphospho(5')adenosine cap structure by an unconventional mRNA capping enzyme of vesicular stomatitis virus.

Authors:  Tomoaki Ogino; Amiya K Banerjee
Journal:  J Virol       Date:  2008-05-21       Impact factor: 5.103

10.  Conservative transcription in three steps visualized in a double-stranded RNA virus.

Authors:  Yanxiang Cui; Yinong Zhang; Kang Zhou; Jingchen Sun; Z Hong Zhou
Journal:  Nat Struct Mol Biol       Date:  2019-11-06       Impact factor: 15.369

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