ARTICLE ABSTRACT
								DOI: 10.1099/vir.0.18952-0
								Online 20 February 2003

Two novel spliced genes in human cytomegalovirus

Parvis Akter,¹ Charles Cunningham,¹ Brian P. McSharry,³ Aidan Dolan,¹ Clare Addison,¹ Derrick J. Dargan,¹ Aycan F. Hassan-Walker,² Vincent C. Emery,² Paul D. Griffiths,² Gavin W. G. Wilkinson³ and Andrew J. Davison¹

¹MRC Virology Unit, Institute of Virology, Church Street, Glasgow G11 5JR, UK
²Department of Virology, Royal Free and University College Medical School, Royal Free Campus, Rowland Hill Street, Hampstead, London NW3 2QG, UK
³Section of Infection and Immunity, University of Wales College of Medicine, Tenovus Building, Heath Park, Cardiff CF14 4XX, UK

Two novel spliced genes (UL131A and UL128) flanking UL130 were predicted from sequence comparisons between human cytomegalovirus (HCMV) and its closest known relative, chimpanzee cytomegalovirus (CCMV), and the splicing patterns were confirmed by mRNA mapping experiments. Both genes were transcribed with late kinetics and shared a polyadenylation site. Comparisons with wild-type HCMV in infected human tissues showed that three of five isolates passaged in cell culture contained disruptions of UL128, one was frameshifted in UL131A and one exhibited a deletion affecting UL131A and UL130. CCMV and the Colburn strain of simian cytomegalovirus, which have been passaged in cell culture, also exhibit disruptions of UL128. These observations indicate that expression of either one of UL128 and UL131A is deleterious to growth of primate cytomegaloviruses in cell culture. Although the functions of these genes are unknown, sequence comparisons suggest that UL128 encodes a -chemokine.

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This article is now available in the May 2003 print issue of JGV (vol. 84, 1117–1122). The complete issue of the journal may be seen in electronic form on JGV Online.