Author:
Muñoz-Lopez Martin,Vilar Raquel,Philippe Claude,Rahbari Raheleh,Richardson Sandra R.,Andres-Anton Miguel,Widmann Thomas,Cano David,Cortes Jose L.,Rubio-Roldan Alejandro,Guichard Etienne,Heras Sara R.,Sanchez-Luque Francisco J.,Morell Maria,Aguilar Elisabet,Garcia-Cañadas Marta,Sanchez Laura,Macia Angela,Vilches Pedro,Nieto-Perez Maria Concepcion,Gomez-Martin Antonio,Gonzalez-Alzaga Beatriz,Aguilar-Garduno Clemente,Ewing Adam D.,Lacasana Marina,Alvarez Ignacio S.,Badge Richard,Faulkner Geoffrey J.,Cristofari Gael,Garcia-Perez Jose L.
Abstract
ABSTRACTLong Interspersed Element 1 (LINE-1/L1) is an abundant retrotransposon that has greatly impacted human genome evolution. LINE-1s are responsible for the generation of millions of insertions in the current human population. The characterization of sporadic cases of mosaic individuals carrying pathogenic L1-insertions, suggest that heritable insertions occurs during early embryogenesis. However, the timing and potential genomic impact of LINE-1 mobilization during early embryogenesis is unknown. Here, we demonstrate that inner cell mass of human pre-implantation embryos support the expression and retrotransposition of LINE −1s. Additionally, we show that LINE-1s are expressed in trophectoderm cells of embryos, and identify placenta-restricted endogenous LINE-1 insertions in newborns. Using human embryonic stem cells as a model of post-implantation epiblast cells, we demonstrate ongoing LINE-1 retrotransposition, which can impact expression of targeted genes. Our data demonstrate that LINE-1 retrotransposition starts very shortly after fertilization and may represent a previously underappreciated factor in human biology and disease.
Publisher
Cold Spring Harbor Laboratory
Cited by
9 articles.
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