The Evolution of Endogenous Viral Elements

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The Evolution of Endogenous Viral Elements Edward C. Holmes  Cell Host & Microbe  Volume 10, Issue 4, Pages 368-377 (October 2011) DOI: 10.1016/j.chom.2011.09.002 Copyright © 2011 Elsevier Inc. Terms and Conditions

Figure 1 Processes Involved in the Generation of EVEs, and How EVEs Can Be Used to Estimate the Age of Viruses, Using Both RNA and DNA Viruses as Examples The presence of EVEs in related species A and B and integrated into the same genomic position such that they are orthologous indicates that this integration event occurred prior to the divergence of these two species (species C is an outgroup). If it is known when species A and B diverged, then the minimum age of the insertion event can also be estimated. See Katzourakis and Gifford (2010) for more details. Figure kindly provided by Rob Gifford. Cell Host & Microbe 2011 10, 368-377DOI: (10.1016/j.chom.2011.09.002) Copyright © 2011 Elsevier Inc. Terms and Conditions

Figure 2 Genomic Structures and Phylogenetic Distribution of Exogenous and Endogenous Bornaviruses, Members of the Order Mononegavirales BDV, exogenous Borna disease virus (shown in red); EBLN, endogenous viruses. For each species, the most intact endogenous elements are shown relative to a representative complete exogenous virus genome. Squares of a specific color on the phylogeny indicate EVEs and the viral gene they represent. Note the bias toward integrated NP sequences. EVEs with poly-A tails are shown, while intact ORFs are marked by an “O” symbol and expressed genes by an “X” symbol. Vertical lines identify noncontiguous genes. Adapted from Katzourakis and Gifford (2010), which should be consulted for more details. Original figure kindly provided by Rob Gifford. Cell Host & Microbe 2011 10, 368-377DOI: (10.1016/j.chom.2011.09.002) Copyright © 2011 Elsevier Inc. Terms and Conditions

Figure 3 Genomic Structures and Phylogenetic Distribution of Exogenous and Endogenous Filoviruses, Members of the Viral Order Mononegavirales ZEBOV, exogenous Ebola virus Zaire (shown in red); TSD, target site duplication. Other labeling is the same as that in Figure 2. Adapted from Katzourakis and Gifford (2010), which should be consulted for more details. Original figure kindly provided by Rob Gifford. Cell Host & Microbe 2011 10, 368-377DOI: (10.1016/j.chom.2011.09.002) Copyright © 2011 Elsevier Inc. Terms and Conditions

Figure 4 Evolution of Exogenous and Endogenous Avian Hepadnaviruses The phylogeny of the bird host species is shown in blue on the left of the figure, while that of the hepadnaviruses (both avian and mammalian) is shown in green on the right. Estimates of divergence time are also shown in both cases; note the huge difference between the time scale of the host (millions of years) and virus (thousands of years) trees. The presence or absence of orthologous eZHBV insertions in various bird species (i.e., eZHBVI, eZHBVj, and eZHBVa) are denoted by the “+” and “−” symbols, respectively, while a question mark means uncertain status. The likely phylogenetic placement of the germline integrations producing eZHBVl and eZHBVa are shown by the green lines connecting the host and virus trees. Using estimated bird host divergence times of 25 MYA and 35 MYA, it is conservatively estimated that the integration of eZHBVa and eZHBVl must have occurred at least 19 MYA, as shown by the dashed line. Adapted from Gilbert and Feschotte (2010), which should be consulted for more details. Original figure kindly provided by Clément Gilbert. Cell Host & Microbe 2011 10, 368-377DOI: (10.1016/j.chom.2011.09.002) Copyright © 2011 Elsevier Inc. Terms and Conditions