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
相关论文
共 59 条
[1]   AMINO-ACID-SEQUENCE OF THE PORCINE, ROTAVIRUS YM VP1 PROTEIN [J].
ALMANZA, L ;
ARIAS, CF ;
LOPEZ, S .
RESEARCH IN VIROLOGY, 1994, 145 (05) :313-317
[2]   VIRUS-PARTICLES IN EPITHELIAL-CELLS OF DUODENAL MUCOSA FROM CHILDREN WITH ACUTE NON-BACTERIAL GASTROENTERITIS [J].
BISHOP, RF ;
DAVIDSON, GP .
LANCET, 1973, 2 (7841) :1281-1283
[3]   ANALYSIS OF THE STRUCTURAL POLYPEPTIDES OF A PORCINE GROUP-C ROTAVIRUS [J].
BREMONT, M ;
COHEN, J ;
MCCRAE, MA .
JOURNAL OF VIROLOGY, 1988, 62 (06) :2183-2185
[4]   SEQUENCES OF THE 4 LARGER PROTEINS OF A PORCINE GROUP-C ROTAVIRUS AND COMPARISON WITH THE EQUIVALENT GROUP-A ROTAVIRUS PROTEINS [J].
BREMONT, M ;
JUSTELESAGE, P ;
CHABANNEVAUTHEROT, D ;
CHARPILIENNE, A ;
COHEN, J .
VIROLOGY, 1992, 186 (02) :684-692
[5]   GROUP-C ROTAVIRUSES IN HUMANS [J].
BRIDGER, JC ;
PEDLEY, S ;
MCCRAE, MA .
JOURNAL OF CLINICAL MICROBIOLOGY, 1986, 23 (04) :760-763
[6]  
BROWN DWG, 1989, LANCET, V2, P737
[7]   GROUP-C ROTAVIRUS ASSOCIATED WITH FATAL ENTERITIS IN A FAMILY OUTBREAK [J].
CAUL, EO ;
ASHLEY, CR ;
DARVILLE, JM ;
BRIDGER, JC .
JOURNAL OF MEDICAL VIROLOGY, 1990, 30 (03) :201-205
[8]   Features of the 3'-consensus sequence of rotavirus mRNAs critical to minus strand synthesis [J].
Chen, D ;
Barros, M ;
Spencer, E ;
Patton, JT .
VIROLOGY, 2001, 282 (02) :221-229
[9]   MYRISTYLATION OF ROTAVIRUS PROTEINS [J].
CLARK, B ;
DESSELBERGER, U .
JOURNAL OF GENERAL VIROLOGY, 1988, 69 :2681-2686
[10]   MOLECULAR-CLONING, SEQUENCE-ANALYSIS AND CODING ASSIGNMENT OF THE MAJOR INNER CAPSID PROTEIN GENE OF HUMAN GROUP-C ROTAVIRUS [J].
COOKE, SJ ;
LAMBDEN, PR ;
CAUL, EO ;
CLARKE, IN .
VIROLOGY, 1991, 184 (02) :781-785