Literature DB >> 2843681

Discontinuous transcription generates heterogeneity at the leader fusion sites of coronavirus mRNAs.

S Makino1, L H Soe, C K Shieh, M M Lai.   

Abstract

Coronavirus mRNA is synthesized by a discontinuous transcription process, which involves a free leader RNA species. As a result, each virus-specific mRNA contains an identical leader RNA derived from the 5', end of the genomic RNA. In this study, we demonstrate by primer extension studies that the leader-fusion sites on a given species of coronavirus subgenomic mRNA are heterogeneous. The heterogeneity was due to variation in the number of pentanucleotide (UCUAA) repeats present at the leader fusion site. This pentanucleotide repeat region was complementary between the free leader RNA and the transcription start sites on the template RNA. This result suggests that the discontinuous transcription of coronavirus mRNAs occurs within the complementary sequences localized in two different RNA segments and that RNA joining occurs at variable sites.

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Year:  1988        PMID: 2843681      PMCID: PMC253535          DOI: 10.1128/JVI.62.10.3870-3873.1988

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


  25 in total

1.  Genomic RNA of the murine coronavirus JHM.

Authors:  H Wege; A Müller; V ter Meulen
Journal:  J Gen Virol       Date:  1978-11       Impact factor: 3.891

2.  RNA of mouse hepatitis virus.

Authors:  M M Lai; S A Stohlman
Journal:  J Virol       Date:  1978-05       Impact factor: 5.103

3.  Evidence for in vivo trans splicing of pre-mRNAs in tobacco chloroplasts.

Authors:  B Koller; H Fromm; E Galun; M Edelman
Journal:  Cell       Date:  1987-01-16       Impact factor: 41.582

4.  A micromethod for detailed characterization of high molecular weight RNA.

Authors:  F S Pedersen; W A Haseltine
Journal:  Methods Enzymol       Date:  1980       Impact factor: 1.600

5.  Sequencing end-labeled DNA with base-specific chemical cleavages.

Authors:  A M Maxam; W Gilbert
Journal:  Methods Enzymol       Date:  1980       Impact factor: 1.600

6.  The replication of murine coronaviruses in enucleated cells.

Authors:  K C Wilhelmsen; J L Leibowitz; C W Bond; J A Robb
Journal:  Virology       Date:  1981-04-15       Impact factor: 3.616

7.  Host cell nuclear function and murine hepatitis virus replication.

Authors:  P R Brayton; R G Ganges; S A Stohlman
Journal:  J Gen Virol       Date:  1981-10       Impact factor: 3.891

8.  A unique cap(m7GpppXm)-dependent influenza virion endonuclease cleaves capped RNAs to generate the primers that initiate viral RNA transcription.

Authors:  S J Plotch; M Bouloy; I Ulmanen; R M Krug
Journal:  Cell       Date:  1981-03       Impact factor: 41.582

9.  Evidence for trans splicing in trypanosomes.

Authors:  R E Sutton; J C Boothroyd
Journal:  Cell       Date:  1986-11-21       Impact factor: 41.582

10.  A trans-spliced leader sequence on actin mRNA in C. elegans.

Authors:  M Krause; D Hirsh
Journal:  Cell       Date:  1987-06-19       Impact factor: 41.582

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  43 in total

1.  Genetic manipulation of arterivirus alternative mRNA leader-body junction sites reveals tight regulation of structural protein expression.

Authors:  A O Pasternak; A P Gultyaev; W J Spaan; E J Snijder
Journal:  J Virol       Date:  2000-12       Impact factor: 5.103

2.  Specificities involved in the initiation of retroviral plus-strand DNA.

Authors:  G X Luo; L Sharmeen; J Taylor
Journal:  J Virol       Date:  1990-02       Impact factor: 5.103

3.  5'-proximal hot spot for an inducible positive-to-negative-strand template switch by coronavirus RNA-dependent RNA polymerase.

Authors:  Hung-Yi Wu; David A Brian
Journal:  J Virol       Date:  2007-01-17       Impact factor: 5.103

4.  Minus-strand copies of replicating coronavirus mRNAs contain antileaders.

Authors:  P B Sethna; M A Hofmann; D A Brian
Journal:  J Virol       Date:  1991-01       Impact factor: 5.103

5.  Replication of murine coronavirus defective interfering RNA from negative-strand transcripts.

Authors:  M Joo; S Banerjee; S Makino
Journal:  J Virol       Date:  1996-09       Impact factor: 5.103

6.  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

7.  High-frequency leader sequence switching during coronavirus defective interfering RNA replication.

Authors:  S Makino; M M Lai
Journal:  J Virol       Date:  1989-12       Impact factor: 5.103

8.  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

9.  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

10.  Genetics of mouse hepatitis virus transcription: evidence that subgenomic negative strands are functional templates.

Authors:  M C Schaad; R S Baric
Journal:  J Virol       Date:  1994-12       Impact factor: 5.103

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