The landscape of human SVA retrotransposons

Abstract SINE-VNTR-Alu (SVA) retrotransposons are evolutionarily young and still-active transposable elements (TEs) in the human genome. Several pathogenic SVA insertions have been identified that directly mutate host genes to cause neurodegenerative and other types of diseases. However, due to thei...

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Published inNucleic acids research Vol. 51; no. 21; pp. 11453 - 11465
Main Authors Chu, Chong, Lin, Eric W, Tran, Antuan, Jin, Hu, Ho, Natalie I, Veit, Alexander, Cortes-Ciriano, Isidro, Burns, Kathleen H, Ting, David T, Park, Peter J
Format Journal Article
LanguageEnglish
Published England Oxford University Press 27.11.2023
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Summary:Abstract SINE-VNTR-Alu (SVA) retrotransposons are evolutionarily young and still-active transposable elements (TEs) in the human genome. Several pathogenic SVA insertions have been identified that directly mutate host genes to cause neurodegenerative and other types of diseases. However, due to their sequence heterogeneity and complex structures as well as limitations in sequencing techniques and analysis, SVA insertions have been less well studied compared to other mobile element insertions. Here, we identified polymorphic SVA insertions from 3646 whole-genome sequencing (WGS) samples of >150 diverse populations and constructed a polymorphic SVA insertion reference catalog. Using 20 long-read samples, we also assembled reference and polymorphic SVA sequences and characterized the internal hexamer/variable-number-tandem-repeat (VNTR) expansions as well as differing SVA activity for SVA subfamilies and human populations. In addition, we developed a module to annotate both reference and polymorphic SVA copies. By characterizing the landscape of both reference and polymorphic SVA retrotransposons, our study enables more accurate genotyping of these elements and facilitate the discovery of pathogenic SVA insertions. Graphical Abstract Graphical Abstract
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ISSN:0305-1048
1362-4962
DOI:10.1093/nar/gkad821