Host Gene Regulation by Transposable Elements: The New, the Old and the Ugly
The human genome has been under selective pressure to evolve in response to emerging pathogens and other environmental challenges. Genome evolution includes the acquisition of new genes or new isoforms of genes and changes to gene expression patterns. One source of genome innovation is from transpos...
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Published in | Viruses Vol. 12; no. 10; p. 1089 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
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26.09.2020
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Abstract | The human genome has been under selective pressure to evolve in response to emerging pathogens and other environmental challenges. Genome evolution includes the acquisition of new genes or new isoforms of genes and changes to gene expression patterns. One source of genome innovation is from transposable elements (TEs), which carry their own promoters, enhancers and open reading frames and can act as ‘controlling elements’ for our own genes. TEs include LINE-1 elements, which can retrotranspose intracellularly and endogenous retroviruses (ERVs) that represent remnants of past retroviral germline infections. Although once pathogens, ERVs also represent an enticing source of incoming genetic material that the host can then repurpose. ERVs and other TEs have coevolved with host genes for millions of years, which has allowed them to become embedded within essential gene expression programmes. Intriguingly, these host genes are often subject to the same epigenetic control mechanisms that evolved to combat the TEs that now regulate them. Here, we illustrate the breadth of host gene regulation through TEs by focusing on examples of young (The New), ancient (The Old), and disease-causing (The Ugly) TE integrants. |
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AbstractList | The human genome has been under selective pressure to evolve in response to emerging pathogens and other environmental challenges. Genome evolution includes the acquisition of new genes or new isoforms of genes and changes to gene expression patterns. One source of genome innovation is from transposable elements (TEs), which carry their own promoters, enhancers and open reading frames and can act as ‘controlling elements’ for our own genes. TEs include LINE-1 elements, which can retrotranspose intracellularly and endogenous retroviruses (ERVs) that represent remnants of past retroviral germline infections. Although once pathogens, ERVs also represent an enticing source of incoming genetic material that the host can then repurpose. ERVs and other TEs have coevolved with host genes for millions of years, which has allowed them to become embedded within essential gene expression programmes. Intriguingly, these host genes are often subject to the same epigenetic control mechanisms that evolved to combat the TEs that now regulate them. Here, we illustrate the breadth of host gene regulation through TEs by focusing on examples of young (The New), ancient (The Old), and disease-causing (The Ugly) TE integrants. The human genome has been under selective pressure to evolve in response to emerging pathogens and other environmental challenges. Genome evolution includes the acquisition of new genes or new isoforms of genes and changes to gene expression patterns. One source of genome innovation is from transposable elements (TEs), which carry their own promoters, enhancers and open reading frames and can act as 'controlling elements' for our own genes. TEs include LINE-1 elements, which can retrotranspose intracellularly and endogenous retroviruses (ERVs) that represent remnants of past retroviral germline infections. Although once pathogens, ERVs also represent an enticing source of incoming genetic material that the host can then repurpose. ERVs and other TEs have coevolved with host genes for millions of years, which has allowed them to become embedded within essential gene expression programmes. Intriguingly, these host genes are often subject to the same epigenetic control mechanisms that evolved to combat the TEs that now regulate them. Here, we illustrate the breadth of host gene regulation through TEs by focusing on examples of young (The New), ancient (The Old), and disease-causing (The Ugly) TE integrants.The human genome has been under selective pressure to evolve in response to emerging pathogens and other environmental challenges. Genome evolution includes the acquisition of new genes or new isoforms of genes and changes to gene expression patterns. One source of genome innovation is from transposable elements (TEs), which carry their own promoters, enhancers and open reading frames and can act as 'controlling elements' for our own genes. TEs include LINE-1 elements, which can retrotranspose intracellularly and endogenous retroviruses (ERVs) that represent remnants of past retroviral germline infections. Although once pathogens, ERVs also represent an enticing source of incoming genetic material that the host can then repurpose. ERVs and other TEs have coevolved with host genes for millions of years, which has allowed them to become embedded within essential gene expression programmes. Intriguingly, these host genes are often subject to the same epigenetic control mechanisms that evolved to combat the TEs that now regulate them. Here, we illustrate the breadth of host gene regulation through TEs by focusing on examples of young (The New), ancient (The Old), and disease-causing (The Ugly) TE integrants. |
Author | Rowe, Helen M. Gould, Poppy A. Enriquez-Gasca, Rocio |
AuthorAffiliation | Centre for Immunobiology, Blizard Institute, Queen Mary University of London, London E1 2AT, UK; r.enriquez-gasca@qmul.ac.uk (R.E.-G.); p.gould@qmul.ac.uk (P.A.G.) |
AuthorAffiliation_xml | – name: Centre for Immunobiology, Blizard Institute, Queen Mary University of London, London E1 2AT, UK; r.enriquez-gasca@qmul.ac.uk (R.E.-G.); p.gould@qmul.ac.uk (P.A.G.) |
Author_xml | – sequence: 1 givenname: Rocio orcidid: 0000-0002-0483-4841 surname: Enriquez-Gasca fullname: Enriquez-Gasca, Rocio – sequence: 2 givenname: Poppy A. orcidid: 0000-0002-6101-9296 surname: Gould fullname: Gould, Poppy A. – sequence: 3 givenname: Helen M. orcidid: 0000-0001-5881-0290 surname: Rowe fullname: Rowe, Helen M. |
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Keywords | KRAB-associated protein 1 endogenous retroviruses gene regulation X chromosome inactivation epigenetic repression genomic imprinting transposable elements Intracisternal A-type particle elements position-effect variegation |
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Snippet | The human genome has been under selective pressure to evolve in response to emerging pathogens and other environmental challenges. Genome evolution includes... |
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SubjectTerms | coevolution DNA methylation DNA Transposable Elements - genetics endogenous retroviruses Endogenous Retroviruses - genetics Enhancers Epigenesis, Genetic - genetics epigenetic repression Epigenetics Evolutionary genetics Gene expression gene expression regulation Gene Expression Regulation - genetics Gene regulation genes Genomes germ cells Humans Intracisternal A-type particle elements Isoforms Long Interspersed Nucleotide Elements - genetics Open reading frames Pathogens position-effect variegation Promoter Regions, Genetic - genetics Proteins Regulatory Sequences, Nucleic Acid - genetics Retroviridae Review Stem cells transposable elements transposons |
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Title | Host Gene Regulation by Transposable Elements: The New, the Old and the Ugly |
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