Abstract
AbstractTransposable elements can cause catastrophic genomic instability and are tightly regulated by the host through multiple restriction pathways. Domesticated elements are derived from these ancestors and have evolved adaptive roles but may retain pathological activity. For example,PEG10is required for placentation but also promotes cancer and neurodegeneration. While much ofPEG10remains poorly understood, a unique feature is its ability to readily form virus-like particles (VLPs) which may contribute to its adaptive and pathological nature. However, comparable restriction networks that antagonize the harmful potential of domesticated genes likePEG10remain unknown. Here, we describe restriction of PEG10 VLP abundance viaUBQLN2and the domesticated retrotransposonRTL8. The gag-likeRTL8antagonizes PEG10 through competitive incorporation into VLPs reminiscent of transposable element inhibitors from diverse eukaryotes. These results represent the first known instance of a retroelement-derived restriction factor antagonizing another domesticated retrotransposon and have implications for our understanding of PEG10 biology.
Publisher
Cold Spring Harbor Laboratory
Cited by
2 articles.
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