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Gene Review

ORF1  -  ORF1 protein

Bos taurus

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Disease relevance of ORF1

  • ORF1 encoded the non-structural and contiguous capsid proteins [1].
  • Among caliciviruses, NB virus shows amino acid identities of 14.1 to 22.6% over the entire ORF-1 nonstructural-protein sequence with NLV, SLV, vesivirus, and lagovirus strains, while the overall sequence identity of the complete NB VP-1 with other caliciviruses is low, varying between 14.6 and 26.7% [2].
  • ORF-1 was transcribed more efficiently in recombinant virus-infected cells than in those infected with OV and analysis of the putative promoter, 5'-AAAATTGTAAATGTA, showed that it was similar to the 7.5-kDa early promoter of vaccinia virus [3].
 

High impact information on ORF1

  • Analysis of the 5' end of transcripts by S1 nuclease and primer extension showed that the transcriptional start points (tsp) of ORF-pp, ORF-1, and ORF-3 in the recombinant were identical or within four nucleotides of the tsps of the same ORFs in OV [3].
  • The 4.4-kb BamHI-E fragment of the orf virus (OV) genome contains three discrete open reading frames designated ORF-pp, ORF-1, and ORF-3, all of which are flanked by vaccinia virus-like early transcriptional control sequences [3].
  • Analyses of the long consensus sequence revealed an extended open reading frame (ORF-1) spanning from base 1,634 to 14,400 that encodes for a putative protein of 4,256 amino acids (approximately 450 kDa) [4].
  • Apart from the ORF1 NTPase region, their ORF1 regions had less than 90% identity to the genogroup III genotype 1 Bo/Jena/80/DE virus, confirming two genogroup III genotypes [5].
  • ORF1 encodes a 334-residue protein almost identical to the putative Rep proteins of previously sequenced S. aureus rolling-circle-replicating plasmids [6].
 

Biological context of ORF1

  • Two ORFs (ORF1 and ORF2) were identified, and their putative transcription initiation and Shine-Dalgarno sequence were localized [6].
 

Associations of ORF1 with chemical compounds

 

Analytical, diagnostic and therapeutic context of ORF1

  • Northern blotting analysis of early RNA isolated from 143B-TK- cells infected with the recombinant virus showed that OV genes were transcribed and that the three transcripts of 0.70-(ORF-pp), 0.48- (ORF1), and 0.75-kb (ORF-3) were the same size as their counterparts in OV-infected cells [3].

References

  1. Genomic characterization of the unclassified bovine enteric virus Newbury agent-1 (Newbury1) endorses a new genus in the family Caliciviridae. Oliver, S.L., Asobayire, E., Dastjerdi, A.M., Bridger, J.C. Virology (2006) [Pubmed]
  2. Characterization of an enteropathogenic bovine calicivirus representing a potentially new calicivirus genus. Smiley, J.R., Chang, K.O., Hayes, J., Vinjé, J., Saif, L.J. J. Virol. (2002) [Pubmed]
  3. In vivo recognition of orf virus early transcriptional promoters in a vaccinia virus recombinant. Fleming, S.B., Mercer, A.A., Fraser, K.M., Lyttle, D.J., Robinson, A.J. Virology (1992) [Pubmed]
  4. Biosynthesis and molecular biology of the secretory proteins of the subcommissural organ. Nualart, F., Hein, S. Microsc. Res. Tech. (2001) [Pubmed]
  5. Complete genomic characterization and antigenic relatedness of genogroup III, genotype 2 bovine noroviruses. Oliver, S.L., Asobayire, E., Charpilienne, A., Cohen, J., Bridger, J.C. Arch. Virol. (2007) [Pubmed]
  6. pBMSa1, a plasmid from a dairy cow isolate of Staphylococcus aureus, encodes a lincomycin resistance determinant and replicates by the rolling-circle mechanism. Loeza-Lara, P.D., Soto-Huipe, M., Baizabal-Aguirre, V.M., Ochoa-Zarzosa, A., Valdez-Alarcón, J.J., Cano-Camacho, H., López-Meza, J.E. Plasmid (2004) [Pubmed]
  7. Construction of a viable BHV1 mutant lacking most of the short unique region. Furth, J.J., Whitbeck, J.C., Lawrence, W.C., Bello, L.J. Arch. Virol. (1997) [Pubmed]
 
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