Reevaluation of Human Cytomegalovirus Coding Potential

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 100; no. 23; pp. 13585 - 13590
• Main Authors: Murphy, Eain, Rigoutsos, Isidore, Shibuya, Tetsuo, Shenk, Thomas E.
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences 11.11.2003; National Acad Sciences
• Subjects: Algorithms; Amino acids; Biological Sciences; Cytomegalovirus; Cytomegalovirus - genetics; Cytomegalovirus - metabolism; DNA; DNA, Viral; Genome; Genomes; Genomics; Human cytomegalovirus; Mice; Microbiology; Models, Genetic; Molecular Sequence Data; Murine cytomegalovirus; Muromegalovirus - genetics; Nucleic acids; Open Reading Frames; Peptides - chemistry; Proteins; Software; Viruses
• ISSN: 0027-8424; 1091-6490; 1091-6490
• DOI: 10.1073/pnas.1735466100

The Bio-Dictionary-based Gene Finder was used to reassess the coding potential of the AD169 laboratory strain of human cytomegalovirus and sequences in the Toledo strain that are missing in the laboratory strain of the virus. The gene-finder algorithm assesses the potential of an ORF to encode a protein based on matches to a database of amino acid patterns derived from a large collection of proteins. The algorithm was used to score all human cytomegalovirus ORFs with the potential to encode polypeptides ≥50 aa in length. As a further test for functionality, the genomes of the chimpanzee, rhesus, and murine cytomegaloviruses were searched for orthologues of the predicted human cytomegalovirus ORFs. The analysis indicates that 37 previously annotated ORFs ought to be discarded, and at least nine previously unrecognized ORFs with relatively strong coding potential should be added. Thus, the human cytomegalovirus genome appears to contain ≈192 unique ORFs with the potential to encode a protein. Support for several of the predictions of our in silico analysis was obtained by sequencing several domains within a clinical isolate of human cytomegalovirus.