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Endogenous retroviruses function as species-specific enhancer elements in the placenta

The mammalian placenta is remarkably distinct between species, suggesting a history of rapid evolutionary diversification(1). To gain insight into the molecular drivers of placental evolution, we compared biochemically predicted enhancers between mouse and rat trophoblast stem cells (TSCs) and find...

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Detalles Bibliográficos
Autores principales: Chuong, Edward B., Rumi, M. A. Karim, Soares, Michael J., Baker, Julie C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3789077/
https://www.ncbi.nlm.nih.gov/pubmed/23396136
http://dx.doi.org/10.1038/ng.2553
Descripción
Sumario:The mammalian placenta is remarkably distinct between species, suggesting a history of rapid evolutionary diversification(1). To gain insight into the molecular drivers of placental evolution, we compared biochemically predicted enhancers between mouse and rat trophoblast stem cells (TSCs) and find that species-specific enhancers are highly enriched for endogenous retroviruses (ERVs) on a genome-wide level. One of these ERV families, RLTR13D5, contributes hundreds of mouse-specific H3K4me1/H3K27ac-defined enhancers that functionally bind Cdx2, Eomes, and Elf5 - core factors that define the TSC regulatory network. Furthermore, we demonstrate that RLTR13D5 is capable of driving gene expression in rat placental cells. Comparison with other tissues revealed that species-specific ERV enhancer activity is generally restricted to hypomethylated tissues, suggesting that tissues permissive to ERV activity gain access to an otherwise silenced source of regulatory variation. Overall, our results implicate ERV enhancer cooption as a mechanism underlying the striking evolutionary diversification of placental development.