Human group C rotavirus: completion of the genome sequence and gene coding assignments of a non-cultivatable rotavirus

被引:22
作者
Chen, ZL
Lambden, PR
Lau, JS
Caul, EO
Clarke, IN
机构
[1] Univ Southampton, Southampton Gen Hosp, Sch Med, Virus Grp, Southampton SO16 6YD, Hants, England
[2] Publ Hlth Lab, Reg Virus Lab, Bristol BS2 8EL, Avon, England
关键词
human group C rotavirus; VP1; VP2; gene-protein coding assignment;
D O I
10.1016/S0168-1702(01)00442-7
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Genome segments I and 2 of human group C rotavirus 'Bristol' strain were sequenced and their gene-protein coding properties assigned. This work completed the genome sequence of a human group C rotavirus (17,910 bp) and allowed the full gene-protein coding assignment of the I I segments of dsRNA. Gene I is 3309 bp in size and contains a single ORF of 3272 nucleotides, encoding a protein of 1090 amino acids in length with a predicted molecular mass of 125 kDa. Comparison of the translated sequence with cognate published mammalian group A, B and C rotavirus sequences showed 45.2, 26.4 and 92.6% identity, respectively. The sequence contains conserved amino acid motifs including the classic RNA-dependent RNA polymerase motif GDD, indicating that segment I encodes the group C rotavirus polymerase protein. Gone 2 is 2736 bp in size and contains a single ORF of 2655 nucleotides encoding a protein of 884 amino acids in length with a calculated molecular mass of 102 kDa. Database searches showed highest homology with VP2, the main structural component of the 'core' from group A rotaviruses (46% identity). Alignment of the human group C and A rotavirus VP2 proteins revealed several characteristics common to nucleic acid binding proteins. However, these features were not shared with group B rotavirus VP2. C) 2002 Published by Elsevier Science B.V.
引用
收藏
页码:179 / 187
页数:9
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