What Doesn't Kill You Makes You Stronger: Transposons as Dual Players in Chromatin Regulation and Genomic Variation

• Published in: BioEssays Vol. 42; no. 4; pp. e1900232 - n/a
• Main Authors: Percharde, Michelle, Sultana, Tania, Ramalho‐Santos, Miguel
• Format: Journal Article
• Language: English
• Published: United States Wiley Subscription Services, Inc 01.04.2020
• Subjects: Animals; Binding Sites; Biological evolution; Chromatin; Chromatin - genetics; chromatin organization; Deoxyribonuclease I - genetics; Deoxyribonucleic acid; Deregulation; DNA; DNA Transposable Elements - genetics; endogenous retroviruses; Enhancer Elements, Genetic; evolution; Evolution, Molecular; Gene Expression; Gene Regulatory Networks; genes; Genetic Variation; Genomes; Genomics; Humans; inflammation; LINE1; Mammals; Mammals - genetics; Mammals - growth & development; mutagenesis; Mutation; preimplantation development; Senescence; transposable elements; Transposons; chromatin organization; endogenous retroviruses; preimplantation development; transposons; LINE1; transposable elements; mutagenesis
• ISSN: 0265-9247; 1521-1878; 1521-1878
• DOI: 10.1002/bies.201900232

Transposable elements (TEs) are sequences currently or historically mobile, and are present across all eukaryotic genomes. A growing interest in understanding the regulation and function of TEs has revealed seemingly dichotomous roles for these elements in evolution, development, and disease. On the one hand, many gene regulatory networks owe their organization to the spread of cis‐elements and DNA binding sites through TE mobilization during evolution. On the other hand, the uncontrolled activity of transposons can generate mutations and contribute to disease, including cancer, while their increased expression may also trigger immune pathways that result in inflammation or senescence. Interestingly, TEs have recently been found to have novel essential functions during mammalian development. Here, the function and regulation of TEs are discussed, with a focus on LINE1 in mammals. It is proposed that LINE1 is a beneficial endogenous dual regulator of gene expression and genomic diversity during mammalian development, and that both of these functions may be detrimental if deregulated in disease contexts. The recent results pointing to a dual role of transposable elements (TEs) as both mutagens and regulators of mammalian development are discussed. Several cellular pathways keep the mutagenic activity of TEs under control, but these pathways can be disrupted by stress. It is proposed that TEs are versatile regulators of chromatin biology that can contribute to evolvability of development.