Gag proteins encoded by endogenous retroviruses are required for zebrafish development

Transposable elements (TEs) make up the bulk of eukaryotic genomes and examples abound of TE-derived sequences repurposed for organismal function. The process by which TEs become coopted remains obscure because most cases involve ancient, transpositionally inactive elements. Reports of active TEs serving beneficial functions are scarce and often contentious due to difficulties in manipulating repetitive sequences. Here, we show that recently active TEs in zebrafish encode products critical for embryonic development. Knockdown and rescue experiments demonstrate that the endogenous retrovirus family BHIKHARI-1 (Bik-1) encodes a Gag protein essential for mesoderm development. Mechanistically, Bik-1 Gag associates with the cell membrane, and its ectopic expression in chicken embryos alters cell migration. Similarly, depletion of BHIKHARI-2 Gag, a relative of Bik-1, causes defects in neural crest development in zebrafish. We propose an "addiction" model to explain how active TEs can be integrated into conserved developmental processes.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2025-04-28
DOI
https://doi.org/10.1073/pnas.2411446122
Citations
11
Primary Topic
Chromosomal and Genetic Variations
Type
article
Field-Weighted Citation Impact
19.25

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article

Gag proteins encoded by endogenous retroviruses are required for zebrafish development

Jonathan N. Wells, Vinh H. Truong, Phillip Schofield, Yi-Chia Huang et al.
11 citations
Proceedings of the National Academy of Sciences
Chromosomal and Genetic Variations
19.25
article

Gag proteins encoded by endogenous retroviruses are required for zebrafish development

Jonathan N. Wells, Vinh H. Truong, Phillip Schofield, Yi-Chia Huang, Cédric Feschotte, Ni‐Chen Chang, Marcos Simões-Costa, Aili Wang
article en
11 citations

Abstract

Transposable elements (TEs) make up the bulk of eukaryotic genomes and examples abound of TE-derived sequences repurposed for organismal function. The process by which TEs become coopted remains obscure because most cases involve ancient, transpositionally inactive elements. Reports of active TEs serving beneficial functions are scarce and often contentious due to difficulties in manipulating repetitive sequences. Here, we show that recently active TEs in zebrafish encode products critical for embryonic development. Knockdown and rescue experiments demonstrate that the endogenous retrovirus family BHIKHARI-1 (Bik-1) encodes a Gag protein essential for mesoderm development. Mechanistically, Bik-1 Gag associates with the cell membrane, and its ectopic expression in chicken embryos alters cell migration. Similarly, depletion of BHIKHARI-2 Gag, a relative of Bik-1, causes defects in neural crest development in zebrafish. We propose an "addiction" model to explain how active TEs can be integrated into conserved developmental processes.

Proceedings of the National Academy of SciencesVol. 122(18)
Boston Children's Hospital (US), Harvard University (US), Cornell University (US), Pediatrics and Genetics (US), Center for Systems Biology (US)
Human Frontier Science Program, National Institutes of Health
Openalex Percentile: Top 1%
Chromosomal and Genetic Variations
19.25
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Gag proteins encoded by endogenous retroviruses are required for zebrafish development — Jonathan N. Wells, Vinh H. Truong, et al. · Proceedings of the National Academy of Sciences (2025) | TGRS Research Map | TGRS