Systematic mutagenesis of large viral genomes such as those of the cyt
omegaloviruses requires strategies for identifying relevant functions
as well as for detailed analysis of particular genes, A number of gene
tic markers that have been developed in other biological systems have
been useful for insertion mutagenesis in these viruses. Thus far, 57 o
f the over 227 genes carried by wild-type human cytomegalovirus have b
een found to be dispensable for growth in cultured cells. Because of t
he limitations on studying human cytomegalovirus in an animal host, th
e closely related murine cytomegalovirus has been used as a surrogate
for pathogenesis, tissue tropism and latency studies in the laboratory
mouse, Genetic analysis of this virus has paralleled work on human cy
tomegalovirus, and an understanding of genes that specifically impact
viral growth in particular organs has emerged from these studies, Stra
tegies for generation of permissive cell lines able to complement esse
ntial human cytomegalovirus replication functions have been described,
and sets of cosmid clones have been used to generate recombinant viru
ses, These methods will enable a systematic functional analysis of the
genomes of human and animal cytomegaloviruses.