Literature DB >> 8388500

Effect of intergenic consensus sequence flanking sequences on coronavirus transcription.

S Makino1, M Joo.   

Abstract

Insertion of a region, including the 18-nucleotide-long intergenic sequence between genes 6 and 7 of mouse hepatitis virus (MHV) genomic RNA, into an MHV defective interfering (DI) RNA leads to transcription of subgenomic DI RNA in helper virus-infected cells (S. Makino, M. Joo, and J. K. Makino, J. Virol. 66:6031-6041, 1991). In this study, the subgenomic DI RNA system was used to determine how sequences flanking the intergenic region affect MHV RNA transcription and to identify the minimum intergenic sequence required for MHV transcription. DI cDNAs containing the intergenic region between genes 6 and 7, but with different lengths of upstream or downstream flanking sequences, were constructed. All DI cDNAs had an 18-nucleotide-long intergenic region that was identical to the 3' region of the genomic leader sequence, which contains two UCUAA repeat sequences. These constructs included 0 to 1,440 nucleotides of upstream flanking sequence and 0 to 1,671 nucleotides of downstream flanking sequence. An analysis of intracellular genomic DI RNA and subgenomic DI RNA species revealed that there were no significant differences in the ratios of subgenomic to genomic DI RNA for any of the DI RNA constructs. DI cDNAs which lacked the intergenic region flanking sequences and contained a series of deletions within the 18-nucleotide-long intergenic sequence were constructed to determine the minimum sequence necessary for subgenomic DI RNA transcription. Small amounts of subgenomic DI RNA were synthesized from genomic DI RNAs with the intergenic consensus sequences UCUAAAC and GCUAAAC, whereas no subgenomic DI RNA transcription was observed from DI RNAs containing UCUAAAG and GCTAAAG sequences. These analyses demonstrated that the sequences flanking the intergenic sequence between genes 6 and 7 did not play a role in subgenomic DI RNA transcription regulation and that the UCUAAAC consensus sequence was sufficient for subgenomic DI RNA transcription.

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Mesh:

Year:  1993        PMID: 8388500      PMCID: PMC237672     

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  35 in total

1.  Mechanism of coronavirus transcription: duration of primary transcription initiation activity and effects of subgenomic RNA transcription on RNA replication.

Authors:  Y S Jeong; S Makino
Journal:  J Virol       Date:  1992-06       Impact factor: 5.103

2.  Coding sequence of coronavirus MHV-JHM mRNA 4.

Authors:  M A Skinner; S G Siddell
Journal:  J Gen Virol       Date:  1985-03       Impact factor: 3.891

3.  Coronavirus minus-strand RNA synthesis and effect of cycloheximide on coronavirus RNA synthesis.

Authors:  S G Sawicki; D L Sawicki
Journal:  J Virol       Date:  1986-01       Impact factor: 5.103

4.  A system for study of coronavirus mRNA synthesis: a regulated, expressed subgenomic defective interfering RNA results from intergenic site insertion.

Authors:  S Makino; M Joo; J K Makino
Journal:  J Virol       Date:  1991-11       Impact factor: 5.103

5.  Identification and characterization of a coronavirus packaging signal.

Authors:  J A Fosmire; K Hwang; S Makino
Journal:  J Virol       Date:  1992-06       Impact factor: 5.103

6.  Sindbis virus proteins nsP1 and nsP2 contain homology to nonstructural proteins from several RNA plant viruses.

Authors:  P Ahlquist; E G Strauss; C M Rice; J H Strauss; J Haseloff; D Zimmern
Journal:  J Virol       Date:  1985-02       Impact factor: 5.103

7.  Coronavirus MHV-JHM: nucleotide sequence of the mRNA that encodes the membrane protein.

Authors:  M Pfleiderer; M A Skinner; S G Siddell
Journal:  Nucleic Acids Res       Date:  1986-08-11       Impact factor: 16.971

8.  Analysis of genomic and intracellular viral RNAs of small plaque mutants of mouse hepatitis virus, JHM strain.

Authors:  S Makino; F Taguchi; N Hirano; K Fujiwara
Journal:  Virology       Date:  1984-11       Impact factor: 3.616

9.  The 5'-end sequence of the murine coronavirus genome: implications for multiple fusion sites in leader-primed transcription.

Authors:  C K Shieh; L H Soe; S Makino; M F Chang; S A Stohlman; M M Lai
Journal:  Virology       Date:  1987-02       Impact factor: 3.616

10.  Defective-interfering particles of murine coronavirus: mechanism of synthesis of defective viral RNAs.

Authors:  S Makino; C K Shieh; J G Keck; M M Lai
Journal:  Virology       Date:  1988-03       Impact factor: 3.616

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  30 in total

1.  Downstream sequences influence the choice between a naturally occurring noncanonical and closely positioned upstream canonical heptameric fusion motif during bovine coronavirus subgenomic mRNA synthesis.

Authors:  A Ozdarendeli; S Ku; S Rochat; G D Williams; S D Senanayake; D A Brian
Journal:  J Virol       Date:  2001-08       Impact factor: 5.103

2.  Coronaviruses maintain viability despite dramatic rearrangements of the strictly conserved genome organization.

Authors:  Cornelis A M de Haan; Haukeline Volders; Cheri A Koetzner; Paul S Masters; Peter J M Rottier
Journal:  J Virol       Date:  2002-12       Impact factor: 5.103

3.  Coronaviruses as vectors: stability of foreign gene expression.

Authors:  Cornelis A M de Haan; Bert Jan Haijema; David Boss; Frank W H Heuts; Peter J M Rottier
Journal:  J Virol       Date:  2005-10       Impact factor: 5.103

4.  The UCUAAAC promoter motif is not required for high-frequency leader recombination in bovine coronavirus defective interfering RNA.

Authors:  R Y Chang; R Krishnan; D A Brian
Journal:  J Virol       Date:  1996-05       Impact factor: 5.103

5.  Analysis of a recombinant mouse hepatitis virus expressing a foreign gene reveals a novel aspect of coronavirus transcription.

Authors:  F Fischer; C F Stegen; C A Koetzner; P S Masters
Journal:  J Virol       Date:  1997-07       Impact factor: 5.103

6.  Coronavirus leader RNA regulates and initiates subgenomic mRNA transcription both in trans and in cis.

Authors:  X Zhang; C L Liao; M M Lai
Journal:  J Virol       Date:  1994-08       Impact factor: 5.103

7.  Requirement of the 5'-end genomic sequence as an upstream cis-acting element for coronavirus subgenomic mRNA transcription.

Authors:  C L Liao; M M Lai
Journal:  J Virol       Date:  1994-08       Impact factor: 5.103

8.  Subgenomic RNA synthesis directed by a synthetic defective interfering RNA of mouse hepatitis virus: a study of coronavirus transcription initiation.

Authors:  R G van der Most; R J de Groot; W J Spaan
Journal:  J Virol       Date:  1994-06       Impact factor: 5.103

9.  Coronaviruses as vectors: position dependence of foreign gene expression.

Authors:  Cornelis A M de Haan; Linda van Genne; Jeroen N Stoop; Haukeline Volders; Peter J M Rottier
Journal:  J Virol       Date:  2003-11       Impact factor: 5.103

10.  Reverse genetic analysis of the transcription regulatory sequence of the coronavirus transmissible gastroenteritis virus.

Authors:  Kristopher M Curtis; Boyd Yount; Amy C Sims; Ralph S Baric
Journal:  J Virol       Date:  2004-06       Impact factor: 5.103

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