Literature DB >> 3973564

Coding sequence of coronavirus MHV-JHM mRNA 4.

M A Skinner, S G Siddell.   

Abstract

A coding sequence at the 5' end of mRNA 4 of the coronavirus MHV-JHM was determined by M13/chain-terminator sequencing of cloned cDNA. An open reading frame of 417 bases with the potential to encode a polypeptide of mol. wt. 15 200 (139 residues) was identified. The 3' end of the open reading frame overlapped by 16 bases the start of an open reading frame found in mRNA 5. The translation product of mRNA 4 was predicted to be a basic polypeptide rich in threonine. It had a large hydrophobic region near the amino terminus and a basic carboxy terminus. An intracellular, virus-specific polypeptide, which has been previously described having a mol. wt. of 14 000 to 14 500 has the size and charge characteristics of such a translation product.

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Year:  1985        PMID: 3973564     DOI: 10.1099/0022-1317-66-3-593

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  28 in total

1.  Translation and processing of mouse hepatitis virus virion RNA in a cell-free system.

Authors:  M R Denison; S Perlman
Journal:  J Virol       Date:  1986-10       Impact factor: 5.103

2.  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

3.  In vitro synthesis of two polypeptides from a nonstructural gene of coronavirus mouse hepatitis virus strain A59.

Authors:  C J Budzilowicz; S R Weiss
Journal:  Virology       Date:  1987-04       Impact factor: 3.616

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

Authors:  S Makino; L H Soe; C K Shieh; M M Lai
Journal:  J Virol       Date:  1988-10       Impact factor: 5.103

5.  Sequence analysis reveals extensive polymorphism and evidence of deletions within the E2 glycoprotein gene of several strains of murine hepatitis virus.

Authors:  S E Parker; T M Gallagher; M J Buchmeier
Journal:  Virology       Date:  1989-12       Impact factor: 3.616

6.  Mutagenic analysis of the coronavirus intergenic consensus sequence.

Authors:  M Joo; S Makino
Journal:  J Virol       Date:  1992-11       Impact factor: 5.103

7.  Mouse hepatitis virus S RNA sequence reveals that nonstructural proteins ns4 and ns5a are not essential for murine coronavirus replication.

Authors:  K Yokomori; M M Lai
Journal:  J Virol       Date:  1991-10       Impact factor: 5.103

8.  Effect of intergenic consensus sequence flanking sequences on coronavirus transcription.

Authors:  S Makino; M Joo
Journal:  J Virol       Date:  1993-06       Impact factor: 5.103

9.  Two murine coronavirus genes suffice for viral RNA synthesis.

Authors:  K H Kim; S Makino
Journal:  J Virol       Date:  1995-04       Impact factor: 5.103

10.  Analysis of constructed E gene mutants of mouse hepatitis virus confirms a pivotal role for E protein in coronavirus assembly.

Authors:  F Fischer; C F Stegen; P S Masters; W A Samsonoff
Journal:  J Virol       Date:  1998-10       Impact factor: 5.103

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