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In rare instances, host genomes domesticate segments of these elements for function. Using a complete human genome assembly and 25 additional vertebrate genomes, we re-analyzed the evolutionary trajectories and functional potential of capsid (CA) genes domesticated from Metaviridae, a lineage of retrovirus-like retrotransposons. Our study expands on previous analyses to unearth several new insights about the evolutionary histories of these ancient genes. We find that at least five independent domestication events occurred from diverse Metaviridae, giving rise to three universally retained single-copy genes evolving under purifying selection and two gene families unique to placental mammals, with multiple members showing evidence of rapid evolution. In the SIRH\/RTL family, we find diverse amino-terminal domains, widespread loss of protein-coding capacity in RTL10 despite its retention in several mammalian lineages, and differential utilization of an ancient programmed ribosomal frameshift in RTL3 between the domesticated CA and protease domains. Our analyses also reveal that most members of the PNMA family in mammalian genomes encode a conserved putative amino-terminal RNA-binding domain (RBD) both adjoining and independent from domesticated CA domains. Our analyses lead to a significant correction of previous annotations of the essential CCDC8 gene. We show that this putative RBD is also present in several extant Metaviridae, revealing a novel protein domain configuration in retrotransposons. Collectively, our study reveals the divergent outcomes of multiple domestication events from diverse Metaviridae in the common ancestor of placental mammals.<\/jats:p>","DOI":"10.1093\/molbev\/msae061","type":"journal-article","created":{"date-parts":[[2024,3,19]],"date-time":"2024-03-19T07:58:56Z","timestamp":1710835136000},"source":"Crossref","is-referenced-by-count":34,"title":["The Diverse Evolutionary Histories of Domesticated Metaviral Capsid Genes in Mammals"],"prefix":"10.1093","volume":"41","author":[{"given":"William S","family":"Henriques","sequence":"first","affiliation":[{"name":"Department of Microbiology and Cell Biology, Montana State University , Bozeman, MT 59717 , USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Janet M","family":"Young","sequence":"additional","affiliation":[{"name":"Basic Sciences Division, Fred Hutchinson Cancer Center , Seattle, WA 98109 , USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Artem","family":"Nemudryi","sequence":"additional","affiliation":[{"name":"Department of Microbiology and Cell Biology, Montana State University , Bozeman, MT 59717 , USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Anna","family":"Nemudraia","sequence":"additional","affiliation":[{"name":"Department of Microbiology and Cell Biology, Montana State University , Bozeman, MT 59717 , USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Blake","family":"Wiedenheft","sequence":"additional","affiliation":[{"name":"Department of Microbiology and Cell Biology, Montana State University , Bozeman, MT 59717 , USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-6005-0016","authenticated-orcid":false,"given":"Harmit S","family":"Malik","sequence":"additional","affiliation":[{"name":"Basic Sciences Division, Fred Hutchinson Cancer Center , Seattle, WA 98109 , USA"},{"name":"Howard Hughes Medical Institute, Fred Hutchinson Cancer Center , Seattle, WA 98109 , USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"286","published-online":{"date-parts":[[2024,3,20]]},"reference":[{"issue":"9","key":"2024042911354167700_msae061-B1","doi-asserted-by":"crossref","first-page":"2104","DOI":"10.1093\/bioinformatics\/bti263","article-title":"ProtTest: selection of best-fit models of protein evolution","volume":"21","author":"Abascal","year":"2005","journal-title":"Bioinformatics"},{"issue":"4","key":"2024042911354167700_msae061-B2","doi-asserted-by":"crossref","first-page":"e0214110","DOI":"10.1371\/journal.pone.0214110","article-title":"The Gag protein PEG10 binds to RNA and regulates trophoblast stem cell lineage specification","volume":"14","author":"Abed","year":"2019","journal-title":"PLoS 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