TY - JOUR TI - Mouse B2 SINE elements function as IFN-inducible enhancers AU - Horton, Isabella AU - Kelly, Conor J AU - Dziulko, Adam AU - Simpson, David M AU - Chuong, Edward B A2 - Levine, Mia T A2 - Przeworski, Molly A2 - Ichiyanagi, Kenji VL - 12 PY - 2023 DA - 2023/05/09 SP - e82617 C1 - eLife 2023;12:e82617 DO - 10.7554/eLife.82617 UR - https://doi.org/10.7554/eLife.82617 AB - Regulatory networks underlying innate immunity continually face selective pressures to adapt to new and evolving pathogens. Transposable elements (TEs) can affect immune gene expression as a source of inducible regulatory elements, but the significance of these elements in facilitating evolutionary diversification of innate immunity remains largely unexplored. Here, we investigated the mouse epigenomic response to type II interferon (IFN) signaling and discovered that elements from a subfamily of B2 SINE (B2_Mm2) contain STAT1 binding sites and function as IFN-inducible enhancers. CRISPR deletion experiments in mouse cells demonstrated that a B2_Mm2 element has been co-opted as an enhancer driving IFN-inducible expression of Dicer1. The rodent-specific B2 SINE family is highly abundant in the mouse genome and elements have been previously characterized to exhibit promoter, insulator, and non-coding RNA activity. Our work establishes a new role for B2 elements as inducible enhancer elements that influence mouse immunity, and exemplifies how lineage-specific TEs can facilitate evolutionary turnover and divergence of innate immune regulatory networks. KW - interferon KW - transposon KW - gene regulation JF - eLife SN - 2050-084X PB - eLife Sciences Publications, Ltd ER -