Analysis of the complete DNA sequence of murine cytomegalovirus

被引:490
作者
Rawlinson, WD
Farrell, HE
Barrell, BG
机构
[1] MRC, MOL BIOL LAB, CAMBRIDGE CB2 2QH, ENGLAND
[2] UNIV CAMBRIDGE, DEPT PATHOL, DIV VIROL, CAMBRIDGE CB2 1TN, ENGLAND
[3] SANGER CTR, CAMBRIDGE CB10 1RQ, ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1128/JVI.70.12.8833-8849.1996
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The complete DNA sequence of the Smith strain of murine cytomegalovirus (MCMV) was determined from virion DNA by using a whole-genome shotgun approach. The genome has an overall G+C content of 58.7%, consists of 230,278 bp, and is arranged as a single unique sequence with short (31-bp) terminal direct repeats and several short internal repeats. Significant similarity to the genome of the sequenced human cytomegalovirus (HCMV) strain AD169 is evident, particularly for 78 open reading frames encoded by the central part of the genome. There is a very similar distribution of G+C content across the two genomes. Sequences toward the ends of the MCMV genome encode tandem arrays of homologous glycoproteins (gps) arranged as two gene families. The left end encodes 15 gps that represent one family, and the right end encodes a different family of 11 gps. A homolog (m144) of cellular major histocompatibility complex (MHC) class I genes is located at the end of the genome opposite the HCMV MHC class I homolog (UL18). G protein-coupled receptor (GCR) homologs (M33 and M78) occur in positions congruent with two (UL33 and UL78) of the four putative HCMV GCR homologs. Counterparts of all of the known enzyme homologs in HCMV are present in the MCMV genome, including the phosphotransferase gene (M97), whose product phosphorylates ganciclovir in HCMV-infected cells, and the assembly protein (M80).
引用
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页码:8833 / 8849
页数:17
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